BIO Flashcards

1
Q

Saturated Fatty Acids prefer use when?

A

-Storage
-When Temp Rises
Packs closer together

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2
Q

Unsaturated Fatty Acids prefer use when?

A

-NRG Production
-When Temp Decreases
Packs further apart

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3
Q

6 Types of Lipids

A

1)Triacylglycerols
2)Fatty Acids
3)Phospholipids
4)Glycolipids
5)Steroids
6)Terpenes

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4
Q

Sphinogolipid

A

When glycerol backbone in phospholipids has N at C2 position (SN2)

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5
Q

Glycolipids versus Phospholipids

A

Polar head group in phospholipids is a sugar in glycolipids

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6
Q

R/S Configuration of AA

A

S except Cysteine is R

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7
Q

T or F R groups involved in secondary structure

A

False, just H bonding

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8
Q

A disulfied bond is considered how many cysteines

A

1, even though 2

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9
Q

Heat as a denature agent?

A

Disrupts all forces

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10
Q

Salt and pH as denaturing agents?

A

Disrupt ion interactions (Na+ + Cl-, H+)

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11
Q

Organic solvents (C+H) as denaturing agents?

A

Disrupt hydrophobic interactions

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12
Q

Urea as denaturing agents?

A

Distrupts H-Bond, denature DNA=RNA

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13
Q

B-mercaptoethanol as a denaturing agent?

A

Distrupts di-sulfide bonds (reducing gels from proteins in lab)

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14
Q

2 Types of protein classes?

A

Structural and Gobular

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15
Q

Glycoprotiens

A

Proteins with some carbphydrateses in membrane

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16
Q

Proteoglycans

A

Greater than 50% carbs on protein in ECM

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17
Q

Cytochromes

A

Proteins with prosthetic heme groups –> Covalently attached in ETC

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18
Q

D for Carbs

A

OH on last chiral carbon is on the R (C6 (CH2OH) on top)

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19
Q

alpha carb ring

A

opposite side OH

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20
Q

L for Carbs

A

OH on last chiral carbon is on the L (C6 (CH2OH) on bottom)

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21
Q

beta carb ring

A

same side OH

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22
Q

Glycogen Branched 1-4

A

Connect horizontal

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23
Q

Glycogen Branched 1-6

A

Connect Verticle

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24
Q

Glycogen linkages

A

Alpha linkages with branching

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25
Q

Starch linkages

A

Alpha linkages with minimal branching
Amylopectin =branching
Amylose = no branching

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26
Q

Cellulose linkages

A

Beta Linkages with no branching

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27
Q

Two forms of starch

A

Amylose and Amylopectin
Amylose = No branching
Amylopectin = Branching

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28
Q

Does positive delta G favour products or reactants?

A

Reactants

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29
Q

Does neg. delta G favour products or reactants?

A

Products

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30
Q

Fat soluble vitamins

A

ADEK

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30
Q

What is transition state?

A

Highest nrg state intermediate not substrate or product

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31
Q

Water soluble vitamins

A

B-Vit, C- Vit, Folate

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32
Q

2 Types of CoFactors

A

1)Organic (Vit)
2)Inorganic (Min)

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33
Q

Prosthetic Group

A

Coenzyme covalently bound to the enzyme

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34
Q

Holoenzyme

A

Active enzyme with bound co-enzyme

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35
Q

Apoenzyme

A

protein part of enzyme

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36
Q

High Km means high or low affinity

A

Low affinity creates substrate

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37
Q

Competitive Inhibitor

A

Enzyme Active Site
Inhibits substrate binding
Increase Km
No Change Vmax

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38
Q

Uncompetitive Inhibitor

A

E-S complex
DOESN”T Inhibits substrate binding
Decrease Km
Decrease Vmax

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39
Q

Mixed Inhibitor

A

E-S complex or Enzyme
DOESN”T Inhibits substrate binding
Decrease/Increase Km
Decrease Vmax

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40
Q

Noncompetitive Inhibitor

A

E-S complex or Enzyme
DOESN”T Inhibits substrate binding
No Change Km
Decrease Vmax

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41
Q

Proteolytic Cleavage

A

Inactive enzymes are irreversibly activated by proteolytic cleave

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42
Q

Reversible Covalent Modification

A

Enzyme activation often via a modifier

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43
Q

Control Protiens

A

Control protiens or portein subunits associate with ezmes to active or inactivate activity

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44
Q

Enzyme Regulation x4

A

-Proteolytic Cleavage
-Reversible Covalent Modification
-Control Proteins
-Allosteric Interactions

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45
Q

Oxidoreductases

A

Catalyzes transfer of electrons

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46
Q

Hydrolases

A

Hyrdolyzes Bond

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47
Q

Lysase

A

Breaks and forms new bonds

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48
Q

Transferases

A

Transfers functional groups

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49
Q

Isomerases

A

Switches configuration of molecule to isomer

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50
Q

Ligases/Synthetases

A

Join molecules together using ATP

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51
Q

Kinases

A

Phosphorylation of target

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52
Q

Phosphatase

A

Dephosphorylation of target

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53
Q

3 Irreversible Steps of Glycolysis

A

1: Glucose to G6P (Hexokinase)
3: F6P to F 1,6, Bisphosphate (PFK)

ATP Used ^^

9: Phosphoenolypyruvate to Pyruvate (Pyruvate Kinase) (ATP Create)

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54
Q

Net Equation Glycolysis

A

1 Glucose + 2 NAD+ + 2ADP + 2Pi
=
2pyruvate + 2NADH + 2H + 2ATP +2H2O

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55
Q

Rxn to create NADH in Glycolysis

A

Glyceraldehyde 3 -Phosphate (2 Molecules) –> 1,3 Bisphosphoglycerate

Via Glyceraldehyde 3 -Phosphate dehydrogenase

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56
Q

2 Energy Generating Steps of Glycolysis

A

5: 1,3 Bisphosphoglycerate –> 3-Phosphoglycerate
(Via Phosphoglycerate Kinase)

9: Phosphoenolyruvate –> Pyruvate
(Via Pyruvate Kinase)

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57
Q

2 Energy using Steps of Glycolysis

A

1: Glucose to G6P (Hexokinase)
3: F6P to F 1,6, Bisphosphate (PFK)

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58
Q

Where does glycolysis occur

A

cytoplasm

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59
Q

Where does krebs cycle occur

A

Mitochondria Matrix

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60
Q

Wher does ETC occur

A

Mitochondria inner membrane

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61
Q

What does the _____ rxn from pyruvate to acetyl-coA produce

A

Oxidation Reaction (oxidizing carbon is the release of O2)

CO2
NADH

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62
Q

Net result of TCA Cycle

A

per 2 Pyruvate (1 Glucose)

2ATP, 6NADH, 2FADH2 +4 CO2 as Biproduct

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63
Q

Substrates of TCA Cycle

A

Oxaloacetate
Citrate
Isocitrate
A-Ketogluterate
Succinyl-CoA
Succinate
Fumarate
Malate

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64
Q

Where complex does NADH come in ETC

A

1

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65
Q

Where complex does FADH come in ETC

A

2

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66
Q

How many NADH pump and ATP create

A

Pumps 10 H+ into intermembrane space
Makes 3 ATP

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67
Q

How many FADH pump and ATP create

A

Pumps 6 H+ into intermembrane space
Makes 2 ATP

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68
Q

True or False Q Enzyme is a Protien Enzyme

A

False Lipid

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69
Q

NADH or FADH is a better reducer?

A

NADH, FADH holds onto its E more

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70
Q

How many does H+ take to produce ATP via ATP Synthase?

A

3 H+ = 1ATP

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71
Q

1 NADH = ___ ATP

A

3
Except in glycolysis only 2 from transport of NADH from cytosol to mito

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72
Q

1 FADH = ___ ATP

A

2

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73
Q

ATP produced Glycolysis total

A

6 ATP

2 NADH x 2= 4 ATP
2 ATP on own

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74
Q

ATP produced pyruvate oxidation

A

6 ATP

2 NADH x 3= 6 ATP

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75
Q

ATP produce Krebs Cycle

A

24 ATP

2 GTP = 2 ATP
6 NADH x 3 =18 ATP
2 FADH x2 = 4 ATP

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76
Q

Why is fermentation used?

A

Hypoxic condition regenerates NAD+ from reducing pyruvate to lactic acid.

In hypoxic conditions, ATP can still be produced in glycolysis, but NAD+ is quickly depleted

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76
Q

Total ATP produced from 1 Glucose molecule (2 turns krebs cycle)

A

36 ATP

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77
Q

How does pyruvate produce NAD+

A

Pyruvate is reduced to Lactic Acid
Pyruvate Carbon is reduced
NADH is oxidized

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78
Q

What is created via the PPP

A

2 NADPH = Fat Synthesis
5 Carbon Sugars Ribose
Products that can be used in glycolysis

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79
Q

What does the first branch of PPP

A

Oxidative Branch
NADPH + CO2
Main regulator via feedback inhibition
Ends with Ribulose-5-Phosphate

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80
Q

What does the second branch of PPP

A

Non-Oxidative Branch
5 Carbon Sugars –> Ribose for creating nucelotides

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81
Q

What are the two options of the PPP

A

1: Create Ribose 5 Phosphate for NUCLEOTIDES
Oxidative and Non-Oxidatve
2: Glycolysis intermediates:
Oxidative –> Non Oxidative to create G-3-P and F-6-P from ribose 5 phopshate

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82
Q

What is the NADPH used for in PPP?

A

Fats Synthesis

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83
Q

Acetyl CoA can be used for?

A

ATP and Fat Synthesis

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84
Q

Where does PPP occur

A

Cytosol

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85
Q

Where does Gluconeogensis occur

A

Cytosol

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86
Q

What is required to be a substrate for gluconeogensis?

A

3-Carbon Structure
Glycolysis/KREBS Intermediate’s

Lactate, Glycerol, Certain AA
NOT Fatty Acid (Cuz made into acetyle Co-A)

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87
Q

What cannot be used as a substrate for gluconeogensis?

A

NOT Fatty Acid (Cuz made into acetyl Co-A, via B-Oxidation)

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88
Q

What is the exception to fatty acids being used as a substrate for gluconeogenesis?

A

Odd chain Fatty acids can be used, last 3 carbons can be used for gluconeogensis

(Rest is used for B-Ox for acteyl CoA)

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89
Q

What is Beta Oxidation

A

Fatty Acid Breakdown to acetyl CoA

Occurs in Mitochondria

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90
Q

Beta Oxidation Equation

A

Step 1:
Fatty Acid + CoA + ATP
=
Acyl CoA +ADP + Pi

Step 2:
ACYL (Carbon) Chain- CoA + FAD + NAD+ +CoA
=
ACYL (Carbon) Chain- CoA (-2 Carbons/OG CoA) + Acetyl CoA (Krebs or Ketones) + NADH +FADH2 (ETC)

Acyl (Carbon) Chain goes until chain is depleted

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91
Q

Fatty acid synthesis occurs in

A

Cytosol

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92
Q

Fatty Acid Synthesis Equation

A

2 Acetyl CoA (glycolysis) + ATP + NADPH (PPP)
(Oxidizing Acetyl CoA)
=
4-C Acyl CoA + CoA +2 NADP + ADP + PI

4-Carbon Acyl continues back by adding 2 more actyl CoA from glycolysis

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93
Q

What is the default Fatty Acid Synthesis Created

A

16 Fatty Acid
Palmitate

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94
Q

Beta- Oxidation occurs how many carbons at a time

A

2

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95
Q

When does Ketogenesis occur?

A

When in a starved state, fatty acids into acetyl CoA.

Absence of insulin (low blood sugar levels), Acetyl CoA converted into Ketones. in Mitochodnira

Ketones can travel on own in blood stream to specific tissues which then absorb it and convert it back to acetyl CoA, then ATP via CAC

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96
Q

T or F Ketone Bodies can be used for gluconeogensis

A

False

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97
Q

Where does ketogensis occur

A

Mitochondria

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98
Q

When does Protein Anabolism Occur x3

A

Fed States
Glycolysis
Glycogenesis
Lipid Storage

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99
Q

When does Protein Catabolism Occur x4

A

Fasting State/UNFED
Gluconeogenesis
Glycogenolyisis
Beta-Oxidation
Ketogenesis

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100
Q

Rate Limiting Enzyme of Glycolysis

A

Phosphofructosekinase-1

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101
Q

Rate Limiting Enzyme Fermentation

A

Lactate Dehydrogenase

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102
Q

Rate Limiting Enzyme Glycogenisis

A

Glycogen Synthase

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103
Q

Rate Limiting Enzyme Glycogenolysis

A

Glycogen Phosphorylase

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104
Q

Rate Limiting Enzyme Gluconeogenesis

A

Fructose 1-6 Bisphosphate

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105
Q

Rate Limiting Enzyme PPP

A

G-6-P Dehydrogenase

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106
Q

Which steps of CAA produce energy carrying products?

A

Isocitrate ==> A-Keto (NADH)
A-Keto –> Succinyl CoA (NADH)
Succinyl CoA –> Succinate (GTP)
Succinate –> Fumerate (FADH2)
Malate –> Oxaloacetate (NADH2)

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107
Q

What is the greatest e-acceptor in ETC?

A

Oxygen, last and therefore takes the most

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108
Q

Gluconeogenesis and Glyogenesis share what enzyme

A

G-6-Phosphotase

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109
Q

What are the 3 substrates for gluconeogenesis?

A

Lactate
Glycerol
Certain AA (Glycolysis and Krebs Cycle Intermediates)

Fatty Acids with last 3 Carbons, No Ketones

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110
Q

What 3 things is the plasma membrane made of?

A
  1. 50% protein
  2. 48% Lipids
  3. 2% Cells
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111
Q

Smooth ER x4

A

Synthesis of Lipids and Sterioids
Carb Metabolism
Detox of Drugs
Ca2+ Regulation

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112
Q

Lysosomes are best in what evnviroment?

A

Acidic

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113
Q

Peroxisome x2

A

Lipid and Protein Storage
DETOX ROS (Reactive Oxidative Species)

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114
Q

T or F all cells have same chemical composition

A

T

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115
Q

T or F Energy flow occurs within cells

A

T

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116
Q

4 Eukaryotic Organsims

A
  1. Protista
    2.Fungi
    3.Plantae
    4.Animalia
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117
Q

What are the 3 things that eukaryotic cells have that prokaryotic don’t

A

1.Membrane Bond Organelles
2.Histones
3.RNA Processing

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118
Q

What is the difference in ribosomes between prokaryotes and eukaryotes?

A

P: Smaller, 30s,50s,70s (ODD)
E: Larger, 40s,60s,80s, (EVEN)

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119
Q

What is the difference in cell wall between prokaryotes and eukaryotes?

A

P: Made of Peptidoglycan
E: IF CW:
- Insects and FUNGI: CHITIM
-Plants: Cellulose

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120
Q

What is the difference in flagella between prokaryotes and eukaryotes?

A

P: Made of Flagellin and Spin
E: Made of Microtubules and Swish

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121
Q

What is the difference in divison between prokaryotes and eukaryotes?

A

P: Binary Fission
E: Mitosis

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122
Q

What is the difference in Genome between prokaryotes and eukaryotes?

A

P: Circular Chromo
E: Liner Chromo

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123
Q

T or F DNA can leave nucleus

A

False, transcription occurs in nucleus and leaves as RNA

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124
Q

What time of enzyme rxn occurs in lysomes

A

Hydrolytic Enzymes

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125
Q

The RER first targets proteins for what organelle

A

Golgi, transmembrane proteins

ALL proteins are tagged to be brought from RER to Golgi via ER lumen

Golgi then sends them to final destinanctin

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126
Q

Proteins that are made for the cytosal are made/translated where?

A

In cytosol, free ribosome

All other are RER (exported from cell or are sequestered in a vesicle)

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127
Q

Golgi Processes what 2 things?

A

Proteins and Lipids

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128
Q

Do all cells have the same amounts of organelles

A

NO, cells that require more energy will have more mito, cells that require more secretion have more RER and golgi

depends on their use

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129
Q

What are the 3 structures of the cytoskeleton (support and movement)?

A
  1. Microfilments
    2.Intermediate Filaments
    3.Microtubules
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130
Q

Role of the Microfilaments/ACTIN?

A

Cell Shape/Support
-Muscle Contraction and Cytokinisis

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131
Q

Role of Intermediate Filaments?

A

Maintain Cell Shape ( STRONGER than Actin)
-Vimentins, Keratin, Lamin

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132
Q

Role of Mictrotublues

A

Intracellular Transport (highways of cells(
-Mitotic Spindles and Cilia,Flagella

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133
Q

Where do microtublues start

A

MTOC and extend from positive end

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134
Q

What are alpha and beta tubule dimers bound to

A

GTP
-B can hydrolyzes the GTP to signal the breakdown of the microtubule

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135
Q

How many microtubules are in a single arrangement?

A

13 protofilimaners (a+b tubule bound to GTP) (A)

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136
Q

How many microtubules are in a double arrangement?

A

23 protofilimaners (a+b tubule bound to GTP)
13 protofilimaners (a+b tubule bound to GTP) (A)
11 protofilimaners (a+b tubule bound to GTP)( B)

9+2 Arrangement of a microtubules (9 bound doublettes and 2 singlettes) in a structure

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137
Q

How many microtubules are in a triple arrangement?

A

33 protofilimaners (a+b tubule bound to GTP)
13(a), 11(b), 11(c)

9+1 Arrangement of a microtubules (9 bound trippletes and 1 singlette) in a structure

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138
Q

When the Mircotubule depolarmizes what happens with concern to GTP?

A

GTP quickly hydrolyzies but a GTP tubulin cap at + end of growing tubule prevents spont. depolyermization (DURING BUILDING OF MT)

When depolrymized the hydroylisis of GTP catches up to the + end and the enture structure collapses

CATASTROPHE

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139
Q

Cilia and Fagella are composed of

A

AXONEME, MT Doublettes (9+2 formation of MT (doublettes and singles)

Doublettes held together by dynein, which causes movement

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140
Q

what does it mean for the lipid bilayer to be assymetric?

A

Phospholipids and protein compositions on the outside and inside of bilayer are structurally and functionally different

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141
Q

Sphingolipids are different from phospholipids how?

A

SN2 of glycerol has N attached
Have a sphingosine group and a fatty acid group instead of 2 fatty acids

Important in mylein

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142
Q

What does cholesterol do in the plasma membrane?

A

Modulates the fluidity of the membrane

-Good @ Hot /High Temp: fills gaps, slows down movement of other membrane components, therefore decreasing membrane fluidity
-COUNTERACTS: good bc MF increases with temp.

-Good @ Cold/Low Temp: spaces our lipids so they cannot constrict as tightly
-COUNTERACTS: Decreases intermolecular force to increase fluidity, cuz with cold fluidity decreases

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143
Q

How are miscelles and membrane different even tho both made of phosplipids

A

Membranes must be actively assembled as they are less thermo stable, compared to miscless which are most stable and form spont.

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144
Q

Hydrophobic or Hydrophilic Molecules can pass through the lipid bilayer?

A

Hydrophobic because interior

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145
Q

The overall diffusion of a molecule across a membrane is determined by

A

Electrochemical gradient
-Chemical Gradient: Concentration (high to low)
-Electrical Gradient: Movement in the direction of the + charged ion would go

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146
Q

Proteins that transverse the membrane are called?

A

Integral Protein (amphipathic)

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147
Q

Proteins associated with integral membrane proteins on the membrane surface are known as?

A

Peripheral or Extrinsic Proteins

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148
Q

Types of Peripheral or Extrinsic Proteins x6

A

-Selective Transport Channel
-Enzyme
-Cell Surface Receptor
-Cell Surface Identify Marker
-Cell Adhesion
-Attachment to the cytoskeleton

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149
Q

Phagocytosis vs. Pinocytosis

A

Phagocytosis = Large Random Transport
Pinocytosis = Small Random Transport

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150
Q

Receptor-Mediated Endocytosis

A

Selective endocytosis
-LDL in cytosol
-LDL receptors on plasma
-Straight to lysomes

(Bring into cell -> Endosome -> Lysosome)

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150
Q

What are the 3 types of junctions that connect animal cells?

A
  1. Tight JXN
    2.Desmosomes
    3.Gap Jxn
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150
Q

What does exocytosis use?

A

It uses secretory vesicles produced by Golgi and release the extracellular fluid of to membrane if transmembrane domain

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151
Q

Transcellular Path v. Para Cellular Path?

A

trans= cross membranes (through 1 cells)
Para = btwn cells

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152
Q

Tight Jxn

A

Form a water tight seal btwn cells that prevents passage of molecules in btw cells

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153
Q

Desmosomes

A

-Join two cells at a single pt and attach directly to the cytoskeleton of each cell
-Hold cells together but do not prevent fluid from circulating the sides
-Tension resistance to a layer of cells.

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154
Q

Gap Jxn

A

CRUCIAL FOR CELL-TO-CELL COMMUNICATION
-Small tunnels connecting cells that allow molecules and ions to move btwn them
-Gap jxn in cardiac muscle allows for the spread of action potential

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155
Q

When will osmosis stop

A

when it reaches dynamic equilibrium, when osmotic pressure is equal to hydrostatic pressure

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156
Q

Osmosis causes water to move from

A

Low solute to high solute
High water to low water
Cross a semipermeable membrane

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157
Q

Tonicity

A

Solute Concentration

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158
Q

Isotonic

A

Same concentration to enviro

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159
Q

Hypertonic

A

More highly concentrated compared to enviro

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160
Q

Hypotonic

A

Less highly concentrated compared to enviro

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161
Q

Simple Diffusion vs. Faciltated Diffusuin

A

Simple: Just passes thru membrane
-Increases linear as it does not depend on anything

Facilitated: Exponential and then level out
-Fast @ Start (low concentration)
-Saturated = Max speed
(relies on amount of transporters)

FOR BOTH NO NRG IS USED

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162
Q

Active Transport

A

Requires energy to pass (the process is going against electrochemical gradient (unnatural))

Gradients created

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163
Q

Primary Active Transport

A

Hydrolysis of ATP takes places directly in order to transport the solute in question

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164
Q

Sodium Potassium Pump is and proccess and net equation

A

Form of Primary Active Transport
3 Na out
3K in
1ATP

  1. Binding of cytoplasm (inside the cell) Na+ to pump triggers phosphorylation by ATP
  2. Phosphorylation causes conformation change in protein
  3. The conformation change expels Na+ to outside and extacellular K+ binds

4.K+ binding triggers the release of phosphate (that came from ATP)

5.Lossof phosphate restores OG conformation

  1. K+ is released and Na sites active again
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165
Q

What is secondary active transport

A

No direct coupling of ATP (established first step)

Step 1: Establish gradient with active transport (H+ gradient)

Step 2: Use H_ gradient to move 2nd substance (desired) into cell

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166
Q

What is the Extra Cellular Matrix (ECM)

A

Extracellular part of animal tissue that provides structural support to cells (LOCATED BTWN CELLS)

Contains: STICK CELLS TOGETER
-proteoglycans
-structural proteins
-adhesive proteins

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167
Q

4 basic types of tissues?

A
  1. Neuro
    2.Connective
    3.Muscle
  2. Epitheilal
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168
Q

Working together of cells heirachy x5

A

1.CELLS
2.TISSUE
3.ORGANS
4.SYSTEMS
5.ORGANSISM

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169
Q

Endosymbiosis theory

A

Bacteria (aerobic) are eaten by Archea (anaerobic) and have a symbiotic relationship over formed eukaryotic cells.

Bacteria live inside hosts (

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170
Q

What are the 3 parts of a virus

A
  1. Genetic Material (DNA/RNA, SS/DS)
  2. Capsid (Protein Coat)
  3. Envelop (Optional, old host membrane to blend in)
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171
Q

What are the subviral particles x2

A

Viroids (naked RNA/plants) and Prions (naked proteins)

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172
Q

What are bacteriophages

A

virus that infects bacteria

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173
Q

How to most virus capsids enter cell

A

Receptor-mediated enocytosis

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174
Q

What do retrovirus contain

A

RNA and Reverse Transcriptase

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175
Q

How do retrovirus work

A
  1. Enter cell via fusion
  2. Reverse Transcription to convert Viral RNA to DNA
  3. Viral DNA enters the hosts gene and is integrated (cannot tell btwn cell OG and Viral DNA now)
  4. Transcription, Translation using cells to make more retrovirus
    5.Ritrovirus released by budding
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176
Q

HIV is what type of virus

A

Retrovirus

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177
Q

What do antiviral do?

A

Target steps of retrovirus before integration

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178
Q

Lytic Cycle: What and what types of virus

A

Replication cycle
Symptomatic
Active cycle replication

Virulant Virus

STRESS go somewhere else

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179
Q

Lysogenic Cycle/ Provirus: What and what types of virus

A

Replication cycle
No Symptoms
Integrated into genome

Temperate virus

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180
Q

How are organisms classified interms of how they aquire carbon and energy

A

Prefix:
-Photo: NRG from Light
-Chemo: NRG form inorganic matter

Suffix:
-Autotroph: Make own carbon source
-Heterotroph: Eat.Consume carbon from other organism

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181
Q

2 Domains of Prokaryotes

A

1.Bacteria
2.Archea

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182
Q

3 distinct of archaea?

A

1.No cell Nucleus
2.No Organelles
3.Extreme Habitat

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183
Q

Bacteria are only anaerobic

A

False, they are both aerobic and anaerobic

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184
Q

What are plasmids

A

In bacteria, small extra-chromo DNA molecules hat may contain genes for antibiotic resistance or virulence factors

-Replicate independant
-Gain or Lost over tie
-Passed to next gene

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185
Q

what does DNA look like in bacteria

A

SINGLE, CIRCULAR, CHROMOSOME of DOUBLE STRANDED DNA

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186
Q

True or False Bacteria have membrane bound organelles

A

False,

Nuc, Mito, Golgi, ER

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187
Q

two “membranes” of bacteria

A
  1. Membrane and everything inside = Protoplast
  2. Cell wall and Capsule = Envelope

Cell wall is required or else protoplast would burst

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188
Q

The cytosol of the bacteria is _____ to the enviro and results in?

A

HYPERTONIC

-Water flows until hydrostatic pressure = osmotic pressure
-Pressure against container = draw into container cuz of solute

Therefore cell wall is needed or else protoplast would burts

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189
Q

Neg. Gram Stain

A

Pink
Thin Cell Wall
Small Petidoglycan between 2 cell membranes

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190
Q

Pos. Gram Stain

A

Purple
Thick Cell Wall
Lots peptidoglycan outside cell

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191
Q

Bacteria Growth is what type

A

Exponential, so doubles each phase
10–>20 –> 40 –> 80–> 160

Each organism produces two daughters

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192
Q

3 types of Bacteria recombination?

A
  1. Conjugation: Me and Zebra
  2. Transformations: Me and dead road kill
  3. Transduction: I get COVID, I infect grace, grace gets covid + paige DNA
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193
Q

Conjugation

A

Bacteria “Sex”
Bacteria join via bridge and transfer

F Plasmid is required (Sex Pili)
F+ = Donor
F-= Acceptor

Single-stranded DNA transfered and the F Plasmid is Nicked

The both bacteria cells synthesisze complemenrary strand to produce doubele stranded circular plasmid and new pili as both are donors

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194
Q

Transformation

A

Picked up “naked” DNA from enviro
LAB PICK UP

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195
Q

Transduction

A

Virus “accidentally” takes some host genome in provirus (come out of genome to enter lytic cyle) next infected cells gets some old host cell DNA

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196
Q

4 Phases of Bacteria Growth

A

1.Lag
2.Exponetial
3.Stationary
4.Death

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197
Q

What is a episome

A

when a F plasmid from conugation is intergated into the main bacterial chromosome

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198
Q

T or F R-Plasmids can conjugate

A

True but have different types of antibiotic resistance to their recipient cells (acceptors)

R= Resistance

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199
Q

What are transposons

A

Transposable Elements
-In P and E
-Genetic elements that can jump around by inserting and deleting themselves from the genome
-TF: Create or Reverse Mutations

Regulated by transponsases

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200
Q

IS Elements

A

Transposase gene flanked by inverted repeated sequences

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201
Q

Complex Transposons

A

Contains the transposes gene followed by REGULATORY GENES

Again the transposons flanked by inverted repeats

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202
Q

Composite Transposons

A

Two Transposase Sequences with a central region btwn them

Inverted repeats flank sequence

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203
Q

The transponses scar is how many BP repeats

A

two

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204
Q

How is regulation different between prokaryotes and eukaryotes?

A

P: Changes due to environment (nutrient availability)
E: Changes due to Homeostasis (Cell)

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205
Q

What is a operan

A

A single promotor to multiple genes
-Region of DNA codes for:
-Promotor, Operator, Genes

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206
Q

What does a operator do?

A

Prevent gene expression of operon (genes) when repressor-bound
-Negative Feedback Regulation (from repressor)
DEFAULT IS NO EXPRESSION

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207
Q

Process of Prokaryotic Regulation

A

WHEN NO LACTOSE PRESENT:
Repressor (lac1) made and binds to operator PREVENTING the RNA polymerase/operon from transcribing lac proteins
(High Glucose, 0 Lactose)
(Low Glucose, 0 Lactose)

WHEN LACTOSE PRESENT: (No glucose)
Repressor (lac1) made and binds to lactose, ALLOWING the RNA polymerase to transcribe/operan activated and lac proteins made
(High Glucose, High Lactose)

(Low Glucose, High Lactose –> CAMP)

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208
Q

Positive Control of Lac Operator

A

Occurs due to LACK of GLUCOSE:
-Need more lactose,
-Low glucose = High cAMP binds to CAP
-CAP activates operan promoter
-Proteins Made

(Low Glucose, High Lactose –> CAMP)

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209
Q

If the carbon 2 (bottom right carbon) on ribose (5c) sugar in DNA is H it is DNA or RNA

A

DNA

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210
Q

If the carbon 2 (bottom right carbon) on ribose (5c) sugar in DNA is OH it is DNA or RNA

A

RNA

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211
Q

Purines

A

A and G
Double ring bases

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212
Q

Pyrimidines

A

T and C
Single Ringed Bases

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213
Q

Differences between purines

A

A has no oxygen
G has Oxygen

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214
Q

Differences between pyimidines

A

T has 3 branches (2 O2)
C has 2 Branches (1 O2)

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215
Q

Nuceloside vs Nucleotide

A

Nucleoside is Nitrogenous base + ribose sugar

Nucleotide is addition of phosphate group

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216
Q

How are nucleotides attached

A

Phophodiester bond (covalent bond between two nucleotides)

Dehydration reaction between the OH attached to the 3’ C of deoxyribose sugar, and the phosphate group attached to the 5’ carbon sugar of the next
(The new nucleotide uses it 5’ PO4 to attached to previous nucleotides 3’ C) HAPPENS 5’ to 3’

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217
Q

How many H Bond bewteen T-A

A

2

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218
Q

How many H bond between G-C

A

3

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219
Q

What two forces stabilize double helix

A

Hydrogen Bonds
Base Stacking (Hydrophobic)

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220
Q

What does it mean that DNA is replicated in a semi-conservative fashion?

A

Each replicatant/daughter contains a strand from parent

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221
Q

Replication in both prok and euk is unidirectional or bidirectional

A

Bidirectional meaning that from replication bubble there are two replication forks leaving each orgin

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222
Q

What regulates replication?

A

Replisome

Attaches to orgin of replication and seperates the two DNA strands and form a replication bubble contain two replication forks

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223
Q

Orgin of Replication EUK versus PROK

A

Multiple Orgins vs Single Orgin

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224
Q

Step 1 Replication

A

Open Helix Via DNA Helicase

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225
Q

Step 2 Replication

A

Hold Helix Open via Single Stranded Binding Protiens

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226
Q

Step 3 Replication

A

Add Primer via RNA Primase

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227
Q

Step 4 Replication

A

Extend DNA off Primer via DNA polymerase 3

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228
Q

Step 5 Replication

A

Remove Primer via DNA Polymerase 1 (Fills DNA)
(in EUK primers removed via RNASE h)
Ozarki Fragements

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229
Q

Step 6 Replication

A

Seal Strands via DNA Ligase

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230
Q

Which enzyme catalyzes DNA Replication and PROOFREEDS

A

DNA Polymerase

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231
Q

DNA polymerase can only add NTD if

A

there is a existing 3’OH

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232
Q

Leading Strand attaches to which antiparallel strand

A

The 5’ -3’ antiparallel strand from start
Works with up with fork

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233
Q

Lagging Strand with Okazi Fragemnet attaches to which antiparallel strand

A

The 3’-5’ antiparallel strand from start
Works down the fork

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234
Q

3 Roles of DNA Polymerase

A

Assembles Leading and Lagging Strands
Removes primer in Prokaryotes
Proofreads

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235
Q

What does RNAse H do?

A

Remove primers in eukaryotes

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236
Q

How are telomeres lengthened different?

A

Ntd lengthened by telomerase instead of DNA Polymerase

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237
Q

4 Ways RNA is different than DNA

A

1)Contains 2 OH on Sugar
2)Single Stranded
3)Contains Uracil and Not Thymine (pairs with A)
4)RNA can leave nucleus

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238
Q

What 2 RNA’s regulate gene expression?

A

1)Small Interferring RNA (siRNA)
2)Micro RNA (miRNA)

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239
Q

What is the difference between mRNA and primary RNA

A

Primary RNA is the product of transcription (immature single strand of mRNA)

mRNA primary transcript is processed to encode a chemical blueprint used in translation (carries info used in translation)

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240
Q

How is transcription regulated

A

1)Transcription Factors
2)upstream/downstream gene regukatory sequences

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241
Q

What is the main regulatory point in gene expression

A

Transcription

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242
Q

What is the TATA box

A

The promoter that initiation factors of transcription find and assemble transcription initation complex

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243
Q

What unzips DNA is transcription

A

RNA polymerase to create TRANSCRIPTION BUBBLE

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244
Q

Transcription is unidirectional or bidirectional

A

Unidirectional and continuous

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245
Q

What has higher and faster proof reading, transcription or DNA replication

A

DNA replication

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246
Q

Transription uses one or two templates

A

1

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247
Q

T or F primers are used in transcription

A

F

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248
Q

What are the 3 post-transcriptional modifications that occur inside the nuceleus

A

1)5’ Cap
2)Poly(A) Tail
3)Splicing

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249
Q

What is the use of the 5’Methyl Guanine Cap

A

Added to the 5’ End of Transcript
Attachment site for protein synthesis and protection from transcript degradation by exonucleases

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250
Q

What is the Poly A Tail

A

3’ End of transcript
String of Adenine nucleotides protecting the 3’ end of transcript from degradation

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251
Q

What is spicing

A

Introns are cleaved out, and exons are spliced together: PRIMARY TRANSCRIPTION.

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252
Q

What enzyme is for splicing

A

snRNPs

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253
Q

What are the 3 traits of the genetic code?

A

1)Unambiguous
-one 3 nucleotide sequence read 5’-3’ on the mRNA strand codes for a specific AA

2)Degenerative
-One AA may have more the one 3 nucleotide sequence

3)Universal
-Nearly every living organism uses the same genetic code

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254
Q

3 Stop Codons

A

UAA: You Are Annoying (Stop)
UAG: You Are Gone (Stop)
UGA: You Go Away (Stop)

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255
Q

1 Start Codons

A

AUG, or MET for AA

Are U Going (START)

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256
Q

What is the Sedimentation Coefficent

A

Ribosome consisting of both the large and small subunits

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257
Q

Sedimentation Coefficient Prok

A

30s +50s = 70s

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258
Q

Sedimentation Coefficient Euk

A

40s + 60s = 80s

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259
Q

What are the 3 sites for translation

A

A: approach
P: Polymerization
E; Exit

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260
Q

The MET in translation starts at what site in translation

A

P

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260
Q

Translation is made in what direction

A

5’->3’
N->C

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261
Q

What is a peptide

A

A small non fxn protein that is made in during the process of translation before protien is finished (transaltion is finished)

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262
Q

Why is there no proofreading in translation

A

There is virtually no proofreading once the translation is underway because hydrolyzing (removing) an incorrect AA would release the peptide from the ribosome.

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263
Q

What happens when a stop codon is met in translation (reaches A site)

A

Release factor bind
(No associated tRNA)

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264
Q

Difference between prokaryotes and eukaryotes translation

A

Prokaryotes: Completes Transcription + Translation same time in cytoplasm

Eukaryotes: Completes transcription and translation at different times, translation in cytoplasm

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265
Q

How does the translation of Membrane-Bound Proteins work?

A
  1. Polypeptide Sequence begins with a free-floating ribosome
  2. The first 20 AA form a signal protein recognized by the SRP
  3. SRP bounds and translation temp stops
  4. SRP carries ribo complex to SRP receptor protien in RER
  5. Translation resume inside RER lumen
  6. Signal protein is removed by cleaving that area of protein
  7. Protein goes under post translation modification in RER
  8. Protien Transported to final target
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266
Q

What are 3 examples of post-translational modifications

A
  1. Folding aided by chaperon proteins
  2. Addition of sugar residues
  3. Additions of lipids and phosphate groups
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267
Q

What happens if post-translational control takes a while or decides proteins are not done and we need protien?

A

Post-translational control have inactive proteins on the READY which can be activated by cleavage phosphorylation

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268
Q

Pt mutations only matter if in what region?

A

Coding

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269
Q

Missense Point Mutation

A

The change causes the codon to code for a different AA (may or may not impact the overall function)

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270
Q

Nonsense Point Mutation

A

The change causes the codon to code for a stop codon (resulting in truncated, usually non-fxn protien)

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271
Q

What are Frameshift Mutations

A

Deletion and Insertion of nucleotides in multiples of 3

Alter the reading frame of the eventual coding region

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272
Q

Insertion mutations only affect the protein sequence if they are not in multiples of ___

A

Multiples of 3 will not change = non-frameshift mutations.

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273
Q

Forward mutations to a already mutated gene will

A

Move it even further from original state (wild type)

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274
Q

Backward mutations to already mutated gene

A

Move it back/revert towards orginal state (wild type)

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275
Q

T or F mutations can be desriable

A

True
may increase fitness of a organism by promoting desirable traits

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276
Q

Large scale mutations are how big and occur where?

A

greater than 1000bp

Occur at the chromosome level

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277
Q

What happens if DNA Repair fails?

A

Cell Apoptosis

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278
Q

When is proofreading capability is at the lowest?

A

Transcription and Translation

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279
Q

What is Cancer the result of?

A

Unrestrained and Uncontrolled growth of cells due to accumulation of mutation.

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280
Q

What are the 3 things that can contribute to cancer?

A

1) Gain of Fxn Mutation (Oncogens via Carcinogens, unstopped cell growth, just keeps going)

2)Loss of Fxn mutatuon (Loss of tumor supressor gene fxn, loss of stop growth capabaility)

3)ROS (reactive oxygen species)

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281
Q

What is the hierarchy of the DNA/Protein complex of chromatin? x5

A
  1. Histones
    2.Nucleosome
    3.Solenoids
    4.Supercoils
  2. Chromatin
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282
Q

What does chromatin attach to form chromosomes

A

Scaffold Proteins

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283
Q

What are the 2 regions of the human chromosomes?

A

Telomere Region: repeating regions of DNA Sequences which protect the ends of each chromosome

Centromere Region: Pt of mitotic spindle attachment during meiosis and mitosis

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284
Q

How many chromosomes do humans have, and what is their shape?

A

23 pairs of homologs (similar but not identical chromosomes), 46 chromosomes total

92 Chromatid

Linear

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285
Q

Euchromatin

A

Contains expressed regions of chromatin and is loosly packadged

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286
Q

Heterochromatin

A

Contains tightly packaged non expressed regions of chromatin

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287
Q

Epigentics

A

Changes that are made around the genome that do not alter the actual nucleotide sequence

-Controls chromatin coiling and uncoiling to regulate which DNA sequences are transcribed

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288
Q

3 Common epigenetic changes

A

1)Histone Modification
-Acetylation, Methylation, Phosphorylation
2)DNA Methylation

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289
Q

2 phases of cell cycle

A

Mitosis
Interphase: G1, S and G2

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290
Q

Go

A

Cell arrest cycle

Most differienated cells enter here

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291
Q

G1

A

Most of time cell is here (or Go)

Normal Cell Acitivity

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292
Q

S

A

DNA replication

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293
Q

G2

A

Normal Cell Activity but double DNA

Checks in replication

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294
Q

Pt of Mitosis

A

Separate sister chromatids (from replication) into 2 genetically identical daughter cells

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295
Q

Prophase x3

A

1.Condensation of chromatin
2.Formation of spindle apparatus
3. Nuclear Envelope Disintegrates

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296
Q

Metaphase

A

Lining up of Chromosomes

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297
Q

Anaphase x2

A

Disjunction and start of cytokinesis

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298
Q

Telophase x4

A

Nuclear envelop reforms
Cytokinesis Cont
Chromosomes condense
Two diploid cells produced

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299
Q

Diploid = Homologous T or F

A

T

There are 46 chromosomes before and 46 chromosome after replication

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300
Q

How are autosomal chromosomes organized and labels?

A

1-22(#)
Largest to Smallest

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301
Q

What triggers epigenetic changes in Chromatin

A

incRNA: long noncoding DNA

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302
Q

If given coding strand how to transribe to RNA

A

Keep strand the same switch A to U

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303
Q

If giving template strand how to transcribe to RNA

A

Transcribe as normal (all and A to U)

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304
Q

How many chromosomes in haploid (gametes)

A

23

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305
Q

How many chromosomes are in diploid germ cells?

A

46 (23 pairs)

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306
Q

When does crossing over occur?

A

Prophase 1
Forms the Synaptonemal Complex

Tetrads (2 Chromosomes) Cross Over

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307
Q

What is a Haplotype

A

A set of alleles or regions of DNA that are inherited together.

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308
Q

In anaphase 1 what are seperated

A

Tetrades, the two homologous chromosomes split
SO, Both chromosomes split, but the chromatid stay together.

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309
Q

When does the law of independent assortment occur?

A

Metaphase 1

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310
Q

3 Ways Eukaryotes increase genetic diversity?

A

1)Crossing over in prophase 1
2)Random assortment in metaphase 1
3)2 Gametes fertilized to produce a unique diploid zygote.

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311
Q

What is nondisjunction

A

Failure of chromosome pairs to separate at anaphase one or sister chromatid to separate at anaphase 2

Results in imbalance of chromosomes, aneuploid

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312
Q

Monosomy

A

Loss of a single chromosome in zygote (45) . Most not viable in nature.

2n-1

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313
Q

Trisomy

A

Addition of a single chromosome in the zygote (47)

2n+1

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314
Q

Turner Syndrome

A

Monosomy of the sex chromosomes (genetically female)

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315
Q

Klinefelters Syndrome

A

Trisomy of the sex chromosomes (XXY: total of 47 chromosomes)

Male

Extra X is a bar body

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316
Q

When is nondisjunction the most impactful

A

Embryogenesis (mitosis)
Offspring cells are affected which multiple to form a body, all cells will have the issue

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317
Q

What are alleles

A

Versions of specific genes

Gene for colour in eyes: alleles are the different colours

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318
Q

The best test offsprings have these qualifications x4

A

1)Small
2)Easy to look after
3)Short Generation time
4)Lots of offspring

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319
Q

Mendalian Ratio is

A

3:1

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320
Q

What is a Test Cross (back cross)

A

Testing for if a dominant trait is it homozygous or heterozygous for the trait

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321
Q

How do test crosses work

A

Breading the individual at question with a homozygous recessive person

If a homozygous recessive trait appears in offspring, it is heterozygous if not its homozygous

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322
Q

Incomplete Dominance

A

The dominant allele does not fully mask reccessive allele
Heterozygous individual shows a intermediate phenotype that is a blend (pink)

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323
Q

Co-dominance

A

There is no intermediate phenotype in the Heterozygote that fully expressed the phenotype of both alleles.

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324
Q

Dihybrid Cross

A

They are used to look at the inheritance pattern of two separate characteristics.

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325
Q

Dihybrid Cross Ratio

A

9:3:3:1

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325
Q

Dihybrid test cross ratio

A

1:1:1:1
Gives all hetrozygotes

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326
Q

What is the dihybrid test cross used for?

A

Confirm the presence of a heterozygous genotype in the F2 progeny of the original dihybrid cross

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327
Q

How does a dihybrid test cross work?

A

Heterozygous F2 Progeny is crossed with homozygous recessive individual –> Gives all heterozygotes

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328
Q

If genes are located on the same chromosome what is the likelihood they will remain together during crossover in prophase 1

A

Indirectly proportional to the distance separating them.
The map units they are apart is the % of how often they are together.

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329
Q

Why does the mosaic pattern occur

A

Barr body formation occurs randomly early in embryonic development and can result in mosaic patterns for females of phenotypic trains on the x chromosome.

tortoise cats or colour vision in females

Parental x activate in some cells and maternal x activated in other cells

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330
Q

Penetrance

A

Probability of a gene or allele being expressed if it is present

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331
Q

Incomplete Penetrance

A

A dominant is not always expressed in the heterozygous indvidual

A recessive allele is not always expressed in homozygous recessive individual

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332
Q

Complete Dominance

A

The penetrance of the dominant allele is 100% and 0% for the recessive allele

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333
Q

Expressivity

A

Degree to which a phenotype is expressed by individuals with the same genotype

-Polyductyl toes in cats
6,7,8,9: different expressivity

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334
Q

Taxonomical Classification

Darn King Philip Cuts Open Five Green Snakes

A

-Domain
-Kingdom
-Phylum
-Class
-Order
-Family
-Genus
-Species

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335
Q

Genus and Species are always in

A

Italics
-genus first
-Species is second

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336
Q

What does hardy-weingberg display

A

No evolution/change in the gene pool of a sexually reproduce population

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337
Q

Hardy-Weinberg 5 conditions

A

1.Large Pop.
2. Mutational Equilibrium (fwd=reverse)
3. No Migration
4. Random Mating
5. No natural selection

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338
Q

Species offspring must be fertile (t/f)

A

True

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339
Q

Speciation

A

A single ancestral species splits into multiple new species or a single species evolves into a reproductively distinct new species

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340
Q

Genetic Drift and Two Types

A

When allele frequency change suddenly and by chance
-Bottleneck
-Founder effect

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341
Q

Bottleneck effect

A

a population contracts to a significantly smaller size due to RANDOM ENVIROMENTAL EFFECT

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342
Q

Founder Effect

A

A small group of individuals leaves a larger population and establishes a new population

The new pop gene pool will reflect the alleles carried by the founders and may be different from the larger pop.

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343
Q

Gene Flow

A

Transfer of alleles from one population to another

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344
Q

Why in inbreeding bad

A

Causes inbreeding depression
-Increased homozygous, decreased heterozygotes
-Decreases genetic diversity
-Increases unfavourable alleles

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345
Q

Outbreeding (out crossing)

A

Increases heterozygotes
-increasing genetic diversity

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346
Q

Differential Reproduction

A

Varying degree of representation of a particular trait across generations

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347
Q

T or F evolution is the same as natural selection

A

False
Evolution is not the same as NS
Natural Selection is a mechanism for evolution
Natural selection is equivalent to survival of the fittest

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348
Q

The molecular clock refers to?

A

Tracking random mutations to help determine where 2 species diverge

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349
Q

Niche

A

All of the abiotic and biotic factors required by a organism

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350
Q

Which is bigger fundamental (idealized set) niche or realized niche (actual)

A

Fundamental is bigger due to competetion btwn organisms for resources

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351
Q

r-selected species

A

Put energy into reproduction over parental care.

Unstable and unpredictable environments

High repro, small body size, early maturity onset, short generation time and ability to disperse offspring widely.

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352
Q

Adaptations of r-selected species

A

little advantage because the enviro is likely to change again.

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353
Q

K-selected species

A

Put energy into ensuring offspring survive

-stable and predictable environments
-predominates because ability to compete successfully for limited resources crucial

-Large body, long life expectancy, ad production of fewer offspring that require extensive parent care , long maturation process

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354
Q

What species (r or K) would u most likely see close to carrying capacity?

A

K

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355
Q

Mendelian Errors

A

Do not fit mendelian ratios
-describe an allele in a indvidual which could have not been recieved from either of its biological parents by mend. inhertance

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356
Q

Adaptive Radiation

A

The evolution of ecological and phenotypic diversity within a lineage

new enviroment to be exploited is an adaptive zone.

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357
Q

Commesnualism

A

relationship one one orgaism benefits and the other is uneffected.

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358
Q

polymorphism

A

When two or more clearly different phenotypes exist in the same population of species.

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359
Q

A and T/U have how many H-Bonds?

A

2

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360
Q

G and C have how many H-Bonds?

A

3

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361
Q

Denaturing occurs because of what?

A

Lost H-Bonds
dsDNA to ssDNA

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362
Q

Primers vs Probes

A

Primers: Bind and Build
-Begin DNA synthesis at a specific site

Probes: Find and Bind
-Bind to DNA sequence and are labelled: radioactive, fluorescent and colourmetric

363
Q

Primers are made of what?

A

DNA (only RNA for replication)

364
Q

Probes are made of what?

A

RNA and DNA

365
Q

Size of Primers compared to Probes

A

Primer are small 18-25 nt
Probes are long 300-700nt

366
Q

What biotech uses Primers? x2

A

PCR
DNA Sequencing

367
Q

What biotech uses probes?x5

A

Northern/Southern Blots
InSitu (FISH AND RNAISH)
Microarrays
RFLP

368
Q

What are the 2 parts of a antibody?

A

Conserved Sequence: Little Variability (where stored)

Variable Sequence: Changes and unique to the specific antigen

369
Q

What is the difference btwn a primary and secondary antibody?

A

Primary = Attaches to Antigen

Secondary = Attaches to Primary to make sequence stronger and faster

370
Q

What are the 8 DNA techniques?

A

1)Gel Electrophoresis
2)Restriction Enzymes/Endonucleases
3)PCR
4)DNA Sequencing
5)Southern Blot
6)RFLP
7)Cloning
8)FISH

371
Q

What type of gel is used for DNA?

372
Q

DNA Gel Electrophoresis

A

RUN A GEL

Separate DNA fragments by size/mass using an electric field.
DNA has a NEG. CHARGE, DNA migrates towards positive anode.

Bigger will move slower

373
Q

Restriction Enzyme/Endonuclease

A

Cut at 4 or 6 bp in a PALLINDROMIC DNA sequence

(palindrome is same 5’ to 3’ on both strands)

374
Q

PCR

A

Photocopy small sections of DNA from a template, create billions of copies via exponential growth of specific sequence

375
Q

DNA Sequencing

A

Sequence by synthesis complementary strand with labelled primer
(determining DNA Sequence)

-Run a modified PCR with one primer
-Run on a Gel
-Determine Sequence Created

376
Q

Southern Blot

A

Detect the presence of a specific DNA sequence in the genome/sample:

-isolate DNA,
-RE digest (chop into smaller pieces)
-Run on gel
-Denature DNA with NaOH (dsDNA- ssDNA)
-Transfer to blot (paper/membrane)
-Probe DNA for target detect probe (where and where it doesn’t bind)

377
Q

RFLP (restriction fragment length polymorphism)

A

Genotype Individuals/Detect Mutations

-Isolate DNA
-RE Digest
-PCR Rxn
-Southern Blot , Probe and Bind fragments
-See sizes (difference in alleles)

378
Q

Cloning

A

Copy DNA (PCR) and ligate into lasmid cDNA ligase => add into new organism p

379
Q

FISH: Fluorescent IN SITU Hybridization

A

Use probe to locate specific DA in cell and check DNA integrity
-IF cell is dying

380
Q

What are the 5 RNA biotech?

A
  1. Gel Elelectrophorisis
  2. RT-PCR (reverse transcriptase)/ q-PCR
    3)Northern Blot
    4)RNAISH
    5)Microarray
381
Q

What Gel is used for RNA

A

Acrylamide Gel (smaller pore size = better size definition)

382
Q

RNA Gel Electrophoresis

A

Separate RNA by mass/size

RNA has Negative Charge

383
Q

RT-PCR / Q-PCR

A

Make cDNA from mRNA (5’UTR, Exons, 3’UTR)

Compare gene expression between sample

384
Q

Northern Blot

A

Quantative

Run a gel,
Transfer to lot
Probe to detect presence

385
Q

RNAISH

A

Detect specific RNA gene expression and location in cell

(Embryo dev)

386
Q

Microarray

A

Compare gene expression between 2 samples

(treatment of thousands of genes simultaneously, increase and decrease expression, done with computer)

387
Q

What are the 6 protein biotech?

A

1)Gel Electrophoresis
2)Western Blot
3)Immunocytochemistry/Immunohistochemistry
4)Chromatography
5)X-ray Crystallography
6)Mass Spectrometry

388
Q

What gel is used for proteins?

A

Acrylamide

389
Q

How is gel electrophrosis different in proteins

A

AA carry positive, neg and neutral charges; therefore different cuz RNA and DNA are just negatuve

390
Q

Isoelectric Focus for Gel Electrophoresis

A

Protiens

-Run small pH gradient gelei; 1st
-Separate by charge (isoelectric pt)

391
Q

Native Gel for Gel Electrophoresis

A

Proteins

No protein denaturing, keep shape and subunits together (compare to denatured)

392
Q

SDS page Gel Electrophoresis

A

Add a negative charge to each AA (denatured and flat), therefore all are now the same(all have neg charge) =

Can solely be Separate by Mass

393
Q

Reducing Gel for Gel Electrophoresis

A

Break disulphide bonds (redox rxn, Beta neothethalyne)

Ensures completely flat (usually paired with SDS)

394
Q

Western Blots

A

Isolate proteins
Run Gel
Transfer to Blot
Use antibody to detect protein

395
Q

Immunocytochemistry/Immunohistochemistry

A

Detect protein with antibodies in cell sample, in sub cell compartments

Location and Expression of Protien

Staining sample

396
Q

Chromatography is what

A

Seperating protiens

397
Q

3 types of protein chromatography

A

Ion Exchange
Size Exclusion/Gel Filtration
Affinity (unique character)

398
Q

X-Ray Crystalliography

A

Find 3D shape of protien

399
Q

Mass Spectroscropy

A

Find Sequence of small peptides, identify protiens

400
Q

True or False Crystallization is used often?

A

False inefficient

401
Q

What are the 3 separation techniques

A

1)Extraction
2)Distillation
3)Crystalization

402
Q

What is Extraction?

A

Seperation based on solubility that invoves 2 not mixable phases (aq layer and less dense organic mixture) l

403
Q

Key moto for extraction

A

Weak before Strong

-Weak Acid removes Strong Base
-Strong Acid removes Weak Base
-Weak Base removes strong acid
-Strong Base removes weak acid

404
Q

What is distillation?

A

Separates compounds based on their differing bp

(must be 20c difference)

-Compound with lower bp will boil off first and can be captured and condensed in cool tube

Fractional distillation if less than 20

405
Q

Crystalization

A

Seperation based on idea that pure substances form crystals more easily than impure substances

406
Q

How does chromatography work?

A

Mixture is dissolved into a solution (mobile phase, carrying sample thru) and poured over matrix

Then it forms distinct layers by drawing out specific compounds and creates a stationary phase

407
Q

Which chromatography separate compounds based on polarity

A

Column
Paper
Thin Layer
High-Pressure Liquid

Polar stays (more interactions, slower), Non-polar fast

407
Q

Salting Out is used in what

A

Ion Exchange Chemotoloy

Percipitate Ions

408
Q

How does Ion exchange chemotology work?

A

Mixture of charge protiens in a solution with charge beads (charge depends on which one you want out)

They solution will seperate (attract and repell)
-Repelled ones at bottom

Then salting out (a buffer) comes in and removes attracted one from stationary phase as buffer replaces
-Come to bottom seprate

409
Q

Mobile Phase

A

The phase in which there is movement. Not stuck the one that is selected to move.

Non polar (cuz polar sticks)
Other Charge (one charge sticked, mobile is free to move)
Affinity binds to one attached and leaves the other to move

410
Q

What 3 things does affinity chromtaology due to result in stationary phase

A

1) Receptor proteins binds to stationary Ligands
2)Enzyme proteins bind to stationary substrate
3)Antibody protein binds to stationary antigen

411
Q

Stationary Phase

A

Behind Bind to, stops from moving, and allows the other thing to move through (mobile phase)

412
Q

T or F SDS Page can also be used to seperate protiens by isoelectric points?

A

True, That is the pH of a particular molecule has no net electric phase

pH gradient is added to gel before the electric gradient

413
Q

Gel Electrophoresis uses what?

A

Non-Spont. Electrolytic Cell

414
Q

Further right on a Gas Chromo means what

A

More Polar

415
Q

Restriction sites must be x2

A

1)Palindromic
2)4 or 6 Nuceotides Long

416
Q

PCR key reagents x5

A

1)DNA template
2)2 DNA Primers
3)Taq polymerase
4)dNTPS
5)mg2+(buffer) to stabilize DNA

417
Q

3 Steps of PCR

A

1)Denature
-raise temp 90-95 break H-bonds btwn strands, now ss DNA template so primers can hybridize

2)Annealing
-Lower temp (50-60), allows the short primer to hybridize w/out the template coming back together (primers binding)

3)Elongation
-Raise temp. to DNA polymerase (TAQ) optimum (70-72)
-Replicate and build new DNA strand
-Synthesis by adding 3’OH of primer

418
Q

4 ways PCR is different than DNA replication

A

1)
PCR: Vitro (test tube) DNA:Vivo (cell)

2)
PCR: DNA Primer Ordered
DNA: RNA primers (s phase, primase makes them)

3)
PCR: Uses heat to denature to get ssDNA
DNA: Uses DNA helicase to break h-bond and denature to get ssDNA

4)
PCR: Amplify small DNA segment
DNA:Entire DNA helix chromosome

419
Q

What is Cell Culture?

A

Process in which cells are are grown under controlled conditions outside the organism

420
Q

What is the growth curve for cell culture

A

Lag Phase
Log phase (exponential, lots of resources and space)
Stationary (cell growth = cell death)
Death Phase (#deaths is greater than # divisios), toxins build up not enough resources

421
Q

The magnification of a microscope is equal to?

A

Mag = Objective (btm) x Ocular (eye 10x)

422
Q

What are the two downsides to a electron microscope?

A

Immobile
In a Vaccum (closed)

423
Q

Diffraction in a microscope is limited to the resolution of what?

A

Approx 0.2 micrometers (0.2 micro/200 nano)

Resolution is distance btwn 2 pts to see as 2 objects

424
Q

Transmission Electron Microscopy is used for

A

Internal cellular structures
-obtain higher resoltuion using a electron beam with small wavelentgh

425
Q

Scanning electron Miscrosy is used for?

A

Surface or 3D structures

426
Q

Light Microscopy can only be used for what? x2

A

Image Dark and Refracting Objects

427
Q

What is Flow Cytometry

A

Used for counting and examining microscopic particles (cells and chromo)

Suspending them in a stream of fluid and passing them through an electronic detection apparatus (stained with flourescents before)

428
Q

4 Steps for DNA extraction

A

1)Cells are broken open to expose the DNA within (cell lysis) by grinding, sonification, or the use of chemicals

2)Membrane lipids are removed by adding a detergent

3)Proteins are digested using a protease

4)Dna is perciptated with a alc

429
Q

How does DNA cloning work

A

1)Plasmid DNA and Foregin DNA are both cut with the same restriction enzyme (sticky ends made complementary to each other)

2)Foreign DNA is inserted into the plasmid where it inactivates the lacz Gene

430
Q

What is needed for DNA cloning x4

A

1)A DNS Plasmid/Vector
2)Gene for Antibiotic Resistance (without plasmid dies)
3)A reporter gene for lac z (conform DNA was inserted into plasmid)
4)Know locations of restricted endonucleases sites

431
Q

How does DNA sequencing work?

A

Sequencing Process for DNA
-DNA to be sequencesd is contained in pure recombinate plasmids and divided into 4 seperate rxn tubes
Template –> Coding

-Each tube contain all nucelotides , DNA polyemerase, and primers complementary to flanking regons of DNA

-Each tube contains one of four ddntps which lack 3’OH terminating sequence

-The fragments undergo gel electrophorisis in 4 seperate lanes (for each ddntp)
-Small fragments appear first (there ddntp) and then large
-Read bottom to top to get sequence (bottom 5’- top3’)

432
Q

In DNA sequencing how do we identify the last base

A

Which ddNTP was added, deduce sequence

433
Q

True or False cDNA has introns?

A

False made from mRNA so it lack introns

But is the same as the DNA without introns

434
Q

What is RT-PCR used for?

A

Used to determine if a gene of interest is actually transcribed in vivo into mRNA.

Tells use whether a given gene is turned on in that tissue or at development pt in time

435
Q

Q-PCR

A

Measure the cDNA template actially avaliable

Does RT-PCR but gives amount not just yes or no if it is activated

436
Q

What is In SITU hybridization?

A

Uses complementary DNA or RNA probe to localize specific DNA or RNA sequence in a portion of tissue (in situ)

Allows research to determine WHERE a given gene is transcribed and integrity

437
Q

Why do we have ctrl for blotting?

A

Use ACTIN or TUBLIN

To ensure equal loading control. Ensure that what you are seeing isn’t just bigger or small by chance, compare to ctrl, they should all be the same size down the row)

438
Q

Immunohistorchemistry

A

Used to determine protein expression

-Secondary antibody with flourscents or enzymes recognizes primary and covery info about expression

-ANTIBODY BIND TO KNOWN PROTEIN

439
Q

What are peptide hormones made of?

A

Amino Acids and Sugars

440
Q

Peptide hormones are polar or nonpolar?

A

Polar, travel easily in blood

441
Q

Polar Hormone characteristics compared to Non-Polar

A

Polar Hormones have a short term fast response

Non-polar are long term and slow acting

442
Q

How are peptide hormones made?

A

RER to Golgi, secretory pathway to plasma membrane

443
Q

How do polar hormones interact with their target?

A

Bind at target cell surface receptor

444
Q

What is GPCR and what is its pathway?

A

Peptide Hormone

GCPR
GProtien
Effector (adenyl cyclase) (convert ATP to cAMP)
Make 2nd Messenger (CAMP)
Activate Target (PKA)

Results in Many protein changes (PKA phosprykates other protiens)

Cell Signal Amplified

445
Q

What is Receptor Tyrosine Kinase (RTK) and its path?

A

Peptide Hormone

RTK
Auto Phosphorylate to activate dimer
Phosphorylated target

Result is increased growth/division

446
Q

Are Steriod Hormones polar or non-polar

447
Q

Where are steroid hormones made?

A

SER or Mitochondira

448
Q

Because sterioid cells are nonpolar how does it effect their transport?

A

Need carrier protiens to travel through blood

At cell can diffuse thru membrane to bind INTERNAL Receptor

449
Q

Where do peptides bind the cell?

450
Q

Where do sterioids bind the cell?

A

cytosol or nucleus

451
Q

What do sterioid hormones do/bind to?

A

Bind to the transcription factor.

Protein binds DNA and changes gene expression

452
Q

What are Tyrosine derived Hormones made of?

453
Q

Where are Tyrosine derived hormones made?

A

Made in cytosol/RER

454
Q

What type of hormones are:

Catecholamines
(Dopamine
Epinephrine/Adrenaline
Noepi/Nor Adrelinaline)

A

Polar Tyrosine Hormones

455
Q

Where are epi/norepi made?

A

Adrenal Medulla

456
Q

What type of hormone are thyroid hormones (T3/T4)

A

Nonpolar Tyrosine Derived Hormones

457
Q

What do T3 and T4 do?

A

CTRL basal metabolic rate

458
Q

Symptoms of Hypothyroid

A

To little T3/T4

Slow Metabolism
Weak
Cold
Loosing Hair

459
Q

Symptoms of Hyperthyroid

A

Too Much T3/T4

Fast Metabolism (underweight)
Hot
Anxious/Irritable

460
Q

What are tropic hormones?

A

Target another endocrine gland

461
Q

What are Direct Hormones?

A

Work on that tissue/gland

462
Q

T or F all hormones need receptors?

A

True

Polar; Outside
Non-polar= Inside

463
Q

Polar Hormones bind to what type of receptor

A

Membrane Receptors

Which then activate a secondary messenger

464
Q

What are the 3 types of hormone membrane receptors

A

1)Enzyme Linked Receptors
2)Ion channel linked receptors (ligand gate channel)
3)G-Protien Coupled Receptors

465
Q

How do G-Protien coupled receptors work?

A

These proteins have 7 Transmembrane Domains and are coupled with a trimeric G protien.

The G protiens have 3 subunits

The alpha subunits binds to GDP in the cell and acts to phosphorylate it into GTPm which allows it to disassociate from rest of G protien

Once activated G proteins are either exciatory of inhibitory depending on their effects in the cell

466
Q

GDP is the active or inactive form

467
Q

GTP is the active or inactive form

468
Q

What are the 3 domains of a G protien

A

Alpha
Beta
Gamma

469
Q

When activated what G protien domain leaves and which stay?

A

Beta and Gamma Stay

Alpha Leaves after binding to GDP phosphorylating to GTP (transition is what allows it to leave)

470
Q

What is the G protein activator

A

G alpha S

Effector (activates next protien)

471
Q

What is the G Protien Inhibitor

A

G alpha I
Inhiboys next protien

472
Q

Enzyme linked receptor is a what

473
Q

Ligand Gated Ion channel has what receptor

A

ACH receptor on muscle

Neuromusclar jxn
Na+ Channel

474
Q

What is a portal system

A

A capillary bed that drains into another capillary bed through a vein, without first goingt through heart

475
Q

What are the 3 portal systems in humans

A

1)Hypothaamic-Hypophyseal portal system (hypothalamus to pitutary land)

2)Hepatic Portal (digestive to liver)

3)Renal Portal (kidneys)

476
Q

How do hormones travel from hypothalamus to ant. pituitary?

A

Bloodstream
-Hypothalamic-Hypophyseal Portal System

477
Q

How do hormones travel from hypothalmus to post. pitutary?

A

Nerve Axons via Neurosecratory Cells
LONG AXONS

478
Q

What two hormones are associated with post. pitutary?

Direct Hormones of Hypothalamus

A

1) ADH/VASOPRESSIN
-Increases H2O absorbtion on collecting ducts

2)Oxytocin
-Releaseed to increase uterine contraction

479
Q

ADH/Vassopressin is Inhibitred by what?

A

Caffine and Alc

480
Q

What are the 7 Hormones of the Ant. Pitutary

A

FLAT PEG

FSH
LH
ACTH
TSH
PRL
Endorphins
GH

481
Q

What is needed for T3 and T4

A

Iodine and TRH stimulaing TSH

482
Q

Every Gland in the body is innevated by the parasympathetic nervous system PNS expect what?

A

Sweat Glands CNS

482
Q

What are the 2 patrs of the adrenal glands

A

Adrenal Cortex
Adrenal Medulla

483
Q

The adrenal cortex responds to ATCH and secretes what?

A

Corticorosteriods

Sugar: Glucorticoids
Salts: Mineralocotricoids
Sex: Corticol Sex hormones

484
Q

What does the adrenal gland secrete?

A

Cateocholamines

Epinephrine and Norepinephrine

485
Q

Glucocorticoids are released where and are associated with what?

A

Released in adrenal cortex

Associated with stress

486
Q

What is the key mineralocoticoid in teh RAAS system?

A

Aldosterone

487
Q

What does aldosterone do?

A

Acts on kidney

Increases Na and Cl retention

Increases K and H secretion

(increases H2O absorption in collecting ducts)

488
Q

How does the RAAS System Work

A

1)When blood volume/pressure decrease JGA cells produce renin

2)Renin converts the plasma protein angiotensinogen (produced in the liver) to angiotensin 1

3)Angiotensin 1 is converted into angiotensin 2

4)Angiotensin 2 stimulates the adrenal cortex to secrete aldosterone

5)Aldosterone increases sodium reabsorption in the kidneys, leading to an increase in blood volume and pressure.

489
Q

What are the chateocholamines

A

Tyrosine Derivative Hormones

Epinephrine/Adrenaline
Norepinephrine/Noradrenaline

490
Q

The secretory cells of the adrenal medulla are part of what system?

A

Sympathetic Nervous System

491
Q

What are the functions of catecholamines?

A

Sympathetic Nervous System (fight or flight)

-Increase HR, Increase Blood Movement
-Decrease Gut, Decrease Excretion
-Increase conversion from glycogen to glucose

492
Q

What Calcitonin?

A

Calictonin is large hormone released by the Thyroid

Decrease Ca2+ levels by inhibiting the release of Ca2+ from bone osteoclasts

493
Q

T3 and T4 increase what?

A

Basal Metabolic Rate

494
Q

Increase blood Ca2+ results in what?

A

Make Calcitonin
Results with increase bone deposition

495
Q

Decrease Blood Ca2+ results in what

A

Make PTH
Results in decreased bone because of reabsorption

496
Q

What does PTH do?

A

Increases blood Ca by stimulating Ca release from bone by osteoclasts

497
Q

Endocrine Glands vs Exocrine Glands

A

Endocrine: secrete their hormone products directly in the blood

Exocrine: Secrete products into ducts that lead directly into the external environment.

498
Q

True or False Somatostatin always inhbits insulin and glucagon

499
Q

Pancreatic Somatostatin is produced by what?

A

Delta Cells

500
Q

Where are Islet of Langerhands?

A

Pancreas
Alpha: Glucagon
Beta: Insulin
Delta: Somatostatin

501
Q

What are the 2 parts of the testes

A

Seminiferous Tubules: Sertoli Cells

Interstitial Cells: Leydig Cells

502
Q

What do Lydig Cells makes?

A

Testosterone

503
Q

What do sertoli cells make?

504
Q

Pathway of Sperm

A

Seven Up

Seminiferous Tubules
Epididymis
Vas Deferens
Ejaculatory
Nothing
Urethra
Penis

505
Q

What happens in the epididymis

A

Spemiogensis
(mature sperm)
(gain flagella, in spermatogensis just round cells)

506
Q

Vasectomy

A

Cut Vas Degerens
No Sperm in Cells

507
Q

What creates the fluid in sperm?

A

Postate
Seminal Vesicle

508
Q

Process of Spermatogenesis x4

A

1) Spermatogenum (stem cells), 2N–>(Mitosis) –> Primary Spermatocytes (2N)

2)Primary Spermatocytes, 2N –> (Meisosis 1) –> Secondary Spermatocyte N Haploid

3)Seondary Spermatocytes N –> (Meiosis 2 )–> Spermatid N

4)Spermatid N –> (Spemogensis/differentiation and maturation) –> Spermatozoa, Sperm, N

509
Q

Acrosome

A

part of sperm; Digest into female cell by enzyme

509
Q

What are primary oocytes (2n) stopped in during meiosis?

A

Prophase 1

509
Q

When does the secondary oocytes (n) stop?

A

Metaphase 2 (meiosis 2)

509
Q

How long does spermatogenesis take?

510
Q

What is expelled during ovulation x2?

A

two daughter cells of equal size
-Secondary Oocyte (n)
-Small Polar Body

511
Q

How many eggs in newborn females

A

2 million primary oocytes (80%die)

512
Q

How many eggs after puberty?

A

400,000 primary oocytes

513
Q

How many secondary oocytes will be expelled via ovulations

514
Q

When the oocyte is expelled from the follicle what does it become

A

Corpus Luteum
Caused by LH

515
Q

What is a zygote

A

Ovum and Spermatozoa

516
Q

Mensturation and Proliferation occur during what phase of ovarian cycle?

A

Proliferatin
(develops and shed)

517
Q

What hormones promote the development of overian follicles?

A

FSH and LH

518
Q

What causes LH surge

A

Follicles secrete estrogen as they grow

Estrogen increases GnRH production

GnRH causes LH and DSH Surge

519
Q

What does the corpus luteum secrete?

A

Estrogen and Progesterone

520
Q

What causes the endometrium to mature in leutal phase

A

Progesterone

521
Q

In the leutal phase what are the inhibitory effects of progesterone and estrogen?

A

Inhibit GnRH, LH, and FH prevent maturation of additional follicles

522
Q

What causes the menses to occur?

A

Drop in progesterone due to atrophy of corpus leuteum

523
Q

What are the 2 layers of cells surrounding the secondary oocyte?

A

Inner: ZonaPellucida
Outer: Corona Radiata

524
Q

What reaction prevents the fusion of other sperm to egg?

A

Cortical Rxn

525
Q

What does pluripotent mean?

A

Ability to develop into any cell type

526
Q

Trophoblast cells become what?

527
Q

Order of zygote to embryo

A

Zygote,

Morula,

Blastocyst (fluid ball) contain ICM (embryo stem cells) and Trophoblasts

Gastrula

Neurula

528
Q

What is the difference between indeterminant cleavage ersus determinant clevagev

A

Indeterminant: Mitotic Division without differentiation

Determinant Cleavage: Mitotic Division with differentiatiom

529
Q

Totipolent?

A

Stem cells become any cell, placenta or embryo
Zygote and Morula

530
Q

Pluripotent

A

Stem cells can become any one of the 3 germ layers (in embryo)

531
Q

Multipotent

A

Stem cells replace cells of a particular lineage, skin, blood, liver

532
Q

What protects the endrometrium

A

Estrogen establishes and Progesteron Protects

533
Q

True of False during the 1st trimester the corpus leutum degrades

A

False preserved by HCG

Keeps progesterone and estrogen levels high preventing new menstrual cycle from occurring

534
Q

When does the corpus leutum degenerate during pregnancy?

A

Second trimester when placenta is fully developed and can produce and secrete estrogen and progesterone on own.

535
Q

What stage does the embryo different into 3 layers

536
Q

What are the 3 layers of the gastrula?

A

Ectoderm
Endoderm
Mesoderm

537
Q

Ectoderm

A

Outer
Integument
Lens of Eyes
Nervous System

538
Q

Endoderm

A

Inner
Epithelial Linings of digestive and resp. tracts
Parts of Liver, Pancreas, Thyroid, Bladder

539
Q

Mesoderm

A

Middle
Musculoskeltelal
Cirulatory
Excretory
Connective
Digestive

540
Q

What layer of gastrula is adrenal cortex derivided

541
Q

What layer of the adrenal medulla derivied?

A

Ectoderm (contains nervous tissue)

542
Q

What is neurulation

A

Notochord in mesoderm induces the ectoderm to thicken and form neural plate

Neural –> Neural Folds –> Neural Tube

543
Q

What does the neural tube become?

A

Spinal Cord, and most of nervous system

544
Q

What does the neural crest become

545
Q

When does embryo become fetus?

A

8 Weeks is on own with placentaand umbiical all stuff o2 and nutrients from mum

546
Q

True or False Mom and Fetus mix blood

A

False no blood mixing

Placenta allows for diffusion between them, gas exchange occurs in placenta, fetus lungs do not work until after birth

547
Q

When is the fetus most suscpetible to factors intefeerrin with development?

A

Organogensis Week 4 to 8

548
Q

1st trimester is classified by

A

Development

549
Q

2nd trimester is classified by

A

Development/Growth

550
Q

3rd trimester is classified by

551
Q

What is blood connective?

A

Connective tissue containing cells and matrix

552
Q

What is blood responsible for? x6

A

Transport of:
1)Nutrients
2)Gases
3)Wastes
4)Hormones
5)Heat
6)Immune Cells

553
Q

3 Components of Blood

A

1)Plasma
2)Buffy Coat (White Blood Cells/Leukocytes and Platelets)
3)Erythocytes

554
Q

What is in Blood Plasma

A

Irons
Urea
Water
Proteins
Organic and Inorganic Compounds

555
Q

3 Common proteins in blood

A

1)Albumin (fatty acid transport)
2)Immunoglobulins (antibodies)
3)Clotting Factors

556
Q

What are Erythrocytes

A

Red Blood Cells, Bag of Hb
No Organelles, No Nucleus, Function in O2 and Co2 transport

557
Q

T or F Erthrocytes have DNA maturity

A

False
No Nucelus or Organelles, not capable of mitosis or reproduction

558
Q

Where are Erythrocytes formed?

A

Formed by bone marrow stem cells

Themopoetic Stem Cells in long bones

559
Q

Leukocytes versus Red Blood Cells

A

W:Organelles but no Hb
R: Hb but no Organelles

560
Q

What is the role of leukocytes?

A

Immune Response

561
Q

What are Platelets

A

Involved in injury repair and derived from small portions of membrane bound cytoplasm

562
Q

The A and B adds what to red blood cell

563
Q

IA and IB are what to i

A

Dominant/Co-Dominant

i is Recessive

564
Q

What is the Rh Factor?

A

Specific antigen present on the surface of the red blood cell

565
Q

Somebody with Rh- blood can receieve blood from who?

A

Only rH- people

566
Q

Can somebody with Rh+ blood receive blood from whom?

567
Q

What are the 2 roles of the Lymphatic system?

A

1)Immune System
2)Secondary Fluid Circulation System

568
Q

The lymph system travels how?

A

One way towards heart

569
Q

4 Functions of Lymph System

A

1)Remove interstitial fluid (return to blood via thoracic duct)

2)Transport Proteins, Large Glycerides, Fatty Acids (chylomicrons)

3)Transport Immune Cells

4)Fluid Balance throughout body (prevent edema)

570
Q

How does the lymph system connect to the circulatory system

A

Lymphatic and Thoracic Ducts

571
Q

What are the 2 components of the immune system?

A

1)Innate Immunity: Non-Specific
-Generalized protection from most invading organsims and toxins

2)Acquired Immunity: Specific
-Protection against specific organisms and toxins

572
Q

3 Forms of Innate Immunity

A

1)Physical Barriers
-Skin, Mucous Membrane

2)Cellular
-PMNs, Monocytes, Macrophages, Esinophiles

3)Chemical Barriers
-pH, Lipids, Enzynes

573
Q

Inflammation is what type of immunity?

574
Q

4 Aspects of inflammation

A

1)Dialation of Blood Vessels
2) Increase permibilty of capillaries
3)Swelling of Tissue
4)Migration of Macrophage/Granuloytes

575
Q

Why does inflammation occur?

A

Response is a protective attempt to stop the stimulus from spreading to other tissues and to initate the healing process (blood Clotting)

576
Q

4 Steps of Blood Response

A

1)At site of damage, platelets adhere to collagen fibers in connective tissue and release a substance that makes nearby platelets sticky

2)Platelets form a plug that provides emergency protecton against blood loss.

3)Plug is reinforced by a clot of cross-linked fibrin formed through a multistep process

4)Fibrin is eventually degraded by plasmin to conclude the healing process

577
Q

3 Types of White Blood Cells

A

1)Agranuclear Monocytes (myeloud stem cells)
2)Granulocytes
(Lymphoid Stem Cells)
3)Agrandular Lymphocytes
(myeloud stem cells)

578
Q

Cells involved in innate immunity are denoted by what?

579
Q

Where to leukocytes derivived from?

A

Pluripotent stem cells in bone marrow
-Myeloid Stem Cells (agran monocytes, Granulocytes)
-Lymphoid Stem Cells (agran lympocytes)

Divided into granular and agranular forms

580
Q

Granulocytes live for a long or short time?

A

Short
Function nonspecifically against infective agents

581
Q

Agranulocytes live for a long or short time?

A

Long
Work against specific agents of infection so they need to hang around in case the same infective agent returns

582
Q

Process of innate immunity?

A
  1. Agranuclear Monocytes

Enter body and are attacked by local macrophages (phagocytes)
-Stimulus activation of acquired immunity

  1. Granulocytes

Neutrophils move toward the infected or injured areas and phagocytize more bacteria

583
Q

What happens when neutrophils and macrophages engulf necrotic tissue and bacetria?

A

Die and form Pus

584
Q

Eosinophils (Myeloid stem cells)

A

Work against parasitic fxn

585
Q

Basophiles (myeloid stem cells)i

A

Relese histamine for the inflammatory responsea

586
Q

Natural Killer Cells (Lymphoid stem cells)

A

Play a major role in the rejection of tumors and cells infected by viruses

-Even if not marked they destory

587
Q

Mast Cells

A

-Wound healing,
-Defense against pathogens
-Allergenic response

588
Q

What are the 2 types of acquired immunity?

A

1)BCells = Humoral
2)TCells =Cell Mediated

589
Q

What do B Cells do?

A

B-Cells produce a singe type of antibody (immunoglobin) which is displayed on the surface of plasma membrane)

590
Q

How are B-Cells activated x2?

A

Free Antigens
Helper T-Cells

591
Q

How does a helper T-Cell activate B cells?

A

1)APC macrophage engulfs bacteria and transports to cell surface

2)Helper T-Cells Reconzes and is activated

3)T-Cell activates B-Cells the produe antibody needed to target that antigen

4)Bcell differeniates into Plasma Cells and Memory B Cells

592
Q

Plasma cells (B cells)

A

Plasma cells synthesis free antibodies and releasing them into the blood

593
Q

Positive Colonal Selection

A

Choose B Cells with antibody to increase relpication of that B cell

594
Q

Negative Colonal Selection

A

Antibody bound to self

Rxn against its own body, auto immune

595
Q

Memory B-Cells

A

Remain in bloodstream to elicit a more immediate response to the antigen upon a secondary exposure

596
Q

What is active immunity

A

Production of memory B cells against a particular antigen is conferred by Vaccination

597
Q

Why do we have booster shots?

A

To induce a secondary response by memory B Cells, increase longeity of the immunity

598
Q

Memory B Cells allow for what response? x2

A

Faster response
Increased concentration

599
Q

Where does the T-Lymphocyte mature

600
Q

How do T-Lymphocytes work?

A

Antibody-like protein receptor that recognizes antigens

601
Q

What happens to T-lymphocytes that reacts to self-antigens?

A

Destroyed in the thalmus

602
Q

Helper T-Cells

A

Recognize APC Macrophage that activates B Cells

603
Q

Memory T-Cells

A

Keep antigen Memory

604
Q

Regulatory T-Cells

A

Suppressors
Negative Feedback for Immune System

605
Q

Cytotoxic T-Cells

A

Bind antigen carrying cell (infected )

Antigen is perforin –> Fills with ions and water –> cell lyselide(bursts)

606
Q

What are Lymph Nodes

A

Filter Lymphs and site of most immune responses

607
Q

What occurs in spleen

A

Filters blood and lymph, stores blood and is a secondary site for immune responses

608
Q

What is the major histocompatibility complex (MHC)

A

Nucleated cells in the human body express MHC.

Membrane-bound proteins that display antigens for recognition by the immune system -

609
Q

MHC class 1 molecules

A

ENDROGENOUS PATHWAY

All Nucleated cells display own metabolism

-Protiens display based on internal workings of cell
-Show weird (infection, cancer, foreign tissues)

610
Q

CD x MHC =

A

8

CD4+ responds to MHC-2 (4x2=8)
CD8+ responds to MHC-1 (8x1=8)

611
Q

MHC Class 2 Molecules

A

EXOGENOUS PATHWAY
-Display extracellular pathogens antigens

-Been phagocytes, been broken down, Displayed

612
Q

4 Steps of endogenous and exogenous pathway?

A
  1. Antigen Uptake (ENDO= IN, EXO=OUT)
  2. Antigen Process
    3.MGC Peptide Association
    4.Cell Surface Expression
613
Q

Path of air in? x12

A

1.External Nares
2.Nasal Passage (Filtered by Nasal hair and Mucous)
3. Pharynx
4.Larynx
5.Epiglottis
6.Glottis
7.Trachea
8.Bronchi
9.Lungs
10.Bronchioles
11.Alveoli
12.Capillaries

614
Q

What is surfactant

A

Covers the alveolus lowering the surface tension of the aveoli and facilitates gas exchange across membrane

615
Q

T or F control the diaphram is soley unconsious

A

False it is concious

616
Q

What presents the lungs from collapsing

A

Pressure differential between intrapleural space and the lungs

617
Q

Ventilation is dependant on pressure changes in what?

A

Thoracic Cavity

618
Q

What seperates the thoracic cavity

619
Q

What is a pneumothrax

A

Pressure inside the intrapleural space increases

620
Q

Increased diffusion in lungs occurs due to what x3

A

Increasing SA
Increasing Pressure Gradient
Decreasing Membrane Thickness

621
Q

When diaphragm contracts what occurs to pressure and volume?

A

Volume increases
Pressure Decreases

622
Q

When does diaphragm contract, inhilation or exhaluation

A

Inhalation

Diaphragm contracts and flattens
External intercostal muscles contract

623
Q

Exhalation is passive or active

A

Passive

Highly elastic/resilient and tend to recoil to their og position

624
Q

Ventilation is regulate by what?

A

Central Chemoreceptors (medulla)e
Peripheral Chemorecptors (carotod artieries and aorta)

Monitor CO2 in blood

625
Q

During inhalation external intercostals go which direction?

A

Up and Out\
Contract

626
Q

During exhalaiom external intercostals go which direction?

A

Relax
Down and In

627
Q

What happens to internal intercostals during forced exhalation?

A

Contracted pull ribcage down

628
Q

What causes the diffusion of O2 into the capillaries and CO2 into the aveoli?

A

Differential partial pressure of O2 and CO2

629
Q

PO2 Lungs

630
Q

PCO2 Lungs

631
Q

Po2 pulmonary cap

632
Q

PCO2 Pulm Cap

A

46mmHG (glucose breakdown increases)

633
Q

Other than gas exchange what are the 4 other functions of the respiratory system?

A

1.Preparation of Inhaled Air
2.Thermoregulation
3.Protection against disease and particulate matter
4.Acid-Base Reg/

634
Q

Right Side of heart delivers blood to what?

635
Q

Left Side of heart delivers blood to what?

636
Q

When atria fill what occurs in terms of pressure and volume

A

RELAX
-Ventrical Relax (distole)

Decreased Pressure, Increased Volume

637
Q

When ventrical contract what occurs in terms of pressure and volume

A

Ventricle Contraction (Systole)

Increased Pressure, Decreased Volume

638
Q

Right Side Heart Path

A

BODY TO LUNGS
1)Superior and Inferior Vena Cava
2)RA
3.Tricuspid Valve (AV)
4.RV
5.Pulmonary (lunar) valve
6. Pulmonary Artery to Lungs

639
Q

Left Side of Heart Path

A

Lungs to Body
1)Pulmonary Vein
2)LA
3)Mitral/Bicuspid Valve *AV
4)LV
5)Aortic Valve (Lunar)
6)Aorta

640
Q

3 branches of aorta?

A
  1. Mesenteric Arteries(Digestive and Liver)
  2. Renal Arteries
    3.Iliac Arteries Bottom

Carotid Artery TOP

641
Q

What causes blood to be proplled through cardio system

A

Hydrostatic Pressure

642
Q

Where and what is the role of the pacemaker/SA node?

A

Right Atrium
Responsible for initating and spread AP for heart contraction

643
Q

What is the electrical flow of the heart?

A

SA Node generate AP (RA)
AP to AV node (Above RV)
Bundle of HIs
Purkinje Fibres

644
Q

True or False the activation of AV node is slow?

A

True allows for the atrium and ventricles to fill

645
Q

Rate of contraction of heart is regulated by what?

646
Q

What is the relationship btwn hydrostatic pressure and osmotic pressure when blood flows into capillary bed (aveolar end)

A

Hydrostatic pressure is greater than osmotic

Net low of fluid occurs out of capillary into intersitution

647
Q

What is the relationship btwn hydrostatic pressure and osmotic pressure when blood flows out of capillary bed (venule end)

A

Hydrostaic pressure decrease (less than osmotic) net fluid flows back into capillary from intersitium

648
Q

What % of fluid is lost in capilary exchange and where does it go

A

10%
Lymphatic System
10 (arterial) - 7 (Venule) = 3 mmHG

649
Q

What is the intersitiium/intersituial fluid

A

Between Tissue Cells

650
Q

Net pressure of blood in arterial end of capillary

A

Blood Pressure (32mmHG)
- Osomtic pressure (22mgHG)

=10mmHG into fluid

651
Q

Net pressure of blood in venule end of capillary?

A

Blood Pressure (15mmHG)
- Osomtic pressure (22mgHG)

=-7mmHG into fluid

652
Q

Osmotic Pressure in capilaries is

653
Q

Why do valves exist in veins

A

Prevent backflow because lower hyrdostatic pressure eists in veins

(less smooth muscle that arteries)

654
Q

How much blood is stored in veins and venules

655
Q

Blood Pressure throughout Circulatory System

A

Decreases from Arterials to capillaries

Stays constant in veins

656
Q

Blood velocity throughout circulatory system

A

Decreases from artieries to capilarries and then increases going to veins *but highest in artieries

Velocity decrease with SA

657
Q

How many O2 does one Hb carry

658
Q

T state Hb versus R state Hb

A

Tstate is low bidning affinity

Rstate is high binding affinity (occurs after 1 O2 has bound)

SHAPE CHANGE

659
Q

Hb binding to Oxygen is what type of curve

A

S (sigmodial curve)

660
Q

What causes a right shifted Hb curve?

A

Increase pCO2, decreasing pH (more H+) and increase in temo

Less bound oxygen at a certain pressure, decreased binding addinity

661
Q

Right shifted Hb curves occur when?

A

Exercising
High Altitude

(less O2)

662
Q

Peripheral tissues is right shifted Hb or Left shifted Hb?

A

Right
Decreased Bidning Affinity

663
Q

Lungs is right shifted Hb or Left shifted Hb?

A

Left
Increased Binding affinity

664
Q

What occurs in a left shifted Hb curve?

A

Decrease CO2
Decreased Temp
Increased pH (less H+)

665
Q

What situation does a left shift Hb occur?

A

Fetal Hb (take O2 from Mom)
CO Poisioning

666
Q

What does 2,3 BPG. 2,3 DPG do?

A

Shift Hb Curve right by binding ti partially deoxygenated Hb to facilitate complete unloading

667
Q

Myoglobin versus Hb

A

Myoglobin has unstant binding affinity but only has one space to hold 1 O2

Single Peptide Chain, 1 Heme Group, Non-cooperative

668
Q

Where does the start digestion of carbs/sugars occur?

A

Mouth via Salivary Amylase

669
Q

What is Bolus

A

Chewing + Salvia (carbs)
Digested by salivary amylase

670
Q

What continues movement down out digestive tract?

A

Peristalis (alt. waves of smooth muscle contraction)

671
Q

Bolus (carbs) combine with stomach juices to form what?

672
Q

How does bolus enter stomach

A

Cardiac Orfice

673
Q

How does chyme leave the stomach and enter duodenum

A

Pylonic Sphincter

674
Q

The duodenun is part of the?

A

Small Intestine

675
Q

What occurs in the small intestine to carbs?

A

Add pancreatic enymes and brush boarder enzymes

676
Q

What happens once carbs are monomers?

A

Absobed into blood stream through enterocytes (intestinal epithelial cell)

677
Q

Where does protein digestion begin

678
Q

4 Cells of the stomach?

A

1.Mucous Cells
2. G Cells
3. Parietal Cells
4. Chief Cells

679
Q

What do mucous cells do?

A

Make mucus to protect stomach cells

680
Q

What do G Cells do?

A

Make Gastrin (peptide hormone)

681
Q

What do Parietal Cells do?

A

Make HCl (acid), lots of Mito

682
Q

Increased activity of parietal cell has what effect on stomach pH

A

Decreases stomach pH (approx.2)

683
Q

What do chief cells do?

A

Make Pepsinogen (zymogen)

684
Q

Pepsinogen (zymogen) combines with HCl to activate what?

685
Q

“Ogen” means what

A

Inactive form

686
Q

What enzyme begins digestion of protiens in stomach

687
Q

What are brush boarder enzymes

A

Amino Pepitdase

688
Q

What activates trypisogen?

A

Enterokinase which is made by brush boarder enzymes in duodenum

689
Q

What are the 5 uses of AA in blood?

A

1.Protein Anabolism (Protein Translation)

Deamination (loss of NH2)
2.Acetyl CoA –> Krebs –> Ox Phos –. ATP synthase
3.Acetyl-Coa –> Fat Synthesis
4.Unfed —> Gluceoneogensis
5.Unfed –> Ketogensis

690
Q

Why is emulsification of lipids required?

A

Because Hydrophobic

691
Q

How are lipids emulsified

692
Q

Where is Bile Made and Storeed

A

Made: Liver
Stored: Gall Bladder

693
Q

What enzyme is produced in the mouth related to fat digestion

A

Lingual Lipase but inactive

694
Q

What activates lingual lipase

695
Q

Where does fat digestion start

A

Can a bit in stomach but mostly in intestine

Emsulifcation occurs there

696
Q

Digested fats and lipids are absorbed into what

A

Lymph not blood stream

697
Q

What are fats digested into x2?

A

1)Fatty Acids FA
2)Monglycerol MGL

698
Q

Where can lymph be reabsorbed into blood

A

Thoracic Duct

699
Q

What 3 enzymes are used for lipid/fat digestion

A
  1. Lingual Lipase STOMACH
  2. Bile (INTESTINES)
  3. Pancreatic Lipase (Intestines)
700
Q

How do fats once digested into MGL and Fatty acids get into lymph?

A

1)Diffuse into enterocytes
2)Go to ER
3)Packaged into chylomicrons
4)Exocytosis released into lymph

701
Q

What are the uses of MGL

A

Glycerol –> Gluceoneogensis

702
Q

What are the uses of FA x5

A

1) Transport: Move to another cell (HDL/LDL)

2)Build Membranes (phospholipids and sphingolipids)

3)Storage: Lipogensis

4)Beta to acetyl coa OX (Krebs)

5)Beta to acetyl coa (Ketogensis)

703
Q

Order of digestive tract?

A

1) Mouth
2) Esphogus
3) Cardiac Sphincter
4)Stomach
5) Pyloric Sphincter
6)Small Intestine (D,I,J)
7)Large Intestine (A, T, D Colons)
8)Sigmoid Colon
9)Rectum
10) anus

704
Q

3 parts of small intestine

A

Duodenum
Illeum
Jejunum

705
Q

3 Parts of Large Intestine

A

Ascending
Transcending
Descedning
Colons

706
Q

A-Amylase (salivary amylase) in the mouth breaks down what

A

Stratch to Polysaccarides

707
Q

Secretions of the stomach cells is stimulated by?

A

PSNS by acetylcholine
Rest and Digest

708
Q

Parietal cells contain many what

A

Mitochondria because requires a lot of energy to produce HCL

709
Q

What does Gastrin Stimulate?

A

Stimulates periatel cells to release HCl

710
Q

What is HCl used for in stomach?

A

Acidic enviroment killing most bacteria

711
Q

What is HCl not effective at killing?

A

HPylori Bacteria
-Gram Neg.
-Causes chronic, gastritis ulcers, stomach cancer

712
Q

What does pepsin do

A

Cleaves peptide bonds of proteins in stomach

713
Q

Where are stomach cells located?

A

Gastric Glands

Gastric Pit (Mucous Cells)

714
Q

What is the cecum?

A

Connects the ileum to ascending colon of large itestine

715
Q

What are the 3 cell types in small intestine?

A

1)Goblet Cells
2)Cyrpts of Leiberkuhn
3)Enterocytes/Epithelial Cells

716
Q

What do Goblet Cells do?

A

Secrete Mucous for Lubrication

717
Q

What do Cyrpts of Leiberkuhn do?

A

Secrete slightly basic pancreatic and intestinal juice

718
Q

What are Enterocytes/Epithelial Cells?

A

Absoprtion of all macromolecules

719
Q

What stimulates the secretion of bile?

A

CCK hormone is response to cyme

Gallbladder releases bile into duodenum via common bile duct

720
Q

What is the role of pancreatic jucie

A

Contain basic bicarbonate which neutralizes acidic chyme in duodenum

721
Q

What is the role of secretin in the duodenum?

A

Release in the response to acidic chyme in duodenum, stimulates the pancreas to secrete pancreatic juice

722
Q

When is secretin secretion stopped?

A

When duodenum pH increases (negative feedback)

723
Q

What are peptidases

A

Released in small intesteine to hydrolize protien

724
Q

What does enterokinase enzyme do and where is it secreted?

A

Secreted for intestinal glands in small intestine
-Converts trypsinogen to trypsin

725
Q

3 Endocrine functions of pancreas?

A

Production of
B=Insulin
a=Glucagon
delta=Somatostatin

726
Q

Pancrease exocrine hormones
released into duodenum by pancreatic duct x6

A

1.Trypsin

2.Pancreatic Amylase (carb hydolysis)

3.Chymotrypsin (protein hydrolysis)

  1. Lipase (lipid hydroylus)
  2. Carboxypeptidase (protein hydrolysis)
  3. Ribonuclease and Deorobonuclease (Nucleic Acid Hyrdolysis)
727
Q

What is the role of trypsin?

A

Protein Hydrolysis and activator of other zymogens

728
Q

What zymogens does trypsin activate? x4

A
  1. Pancreatic Amylase
    2.Chymotrypsinogen
    3.Lipase
    4.Carboxypepitdase
729
Q

What are the 2 major functions of the large intestine?

A

Water Reabsorbtion
Electrolyte Absorption

730
Q

What is constipation

A

Excessive water re-absoption

731
Q

What is diarrehea

A

Failure of LI to reabsorb water

732
Q

Fibre (cellulose) is not digested by human but is digested by?

A

Our microbiome

733
Q

Where does absorption of nurtrients occur?

A

Small Intestine

734
Q

How does carbohydrate absorption work?

A

1.Travel from the intestinal lumen (pancreatic amylase (those not done by salivary amylase) and brush border to monomers)

  1. Through the enterocyte
  2. To the Basolateral Side (faciliated diffusiin) to portal vein and then the liver
735
Q

Fructose absoprtion into enterocyte is caused by what

A

GLUT 5 Transporter, faciltated diffusion

736
Q

Glucose and Galactose absorption into enterocyte is caused by what?

A

SGLT1

Also bring Na in

737
Q

How is a gradient created in the enterocyte?

A

Sodium K pump

Decrease sodium concentration

738
Q

How are carb monomers released into portal vein (basolateral side)?

A

Facilitated diffusion (GLUT 2 Transporter)

739
Q

What is the by produce of deamination and what occurs to it?

A

Ammonia

Converted by the liver to urea and excreted as urine in kidney

740
Q

How does protein absorption work?

A

1) Protiens hydrolyzed to polypeptides by pepsin in the stomach

2)Intestinal Lumen: Brush Boarder, Trypsin and Chymotrypsin hydrolyze polypeptides to aa, di peptides, tripeptides

3)Enter enterocyte via facilitated and active transport (all converted do AA)

4)Enter basolateral side (via facilitated diffusion) , Portal Vein and Liver

741
Q

How does Fat absorption work?

A

1)Intestinal Lumen
-Bile Emuslifies into micelles
-Lipase hydrolyze triglycerides into fatty acids
-Monoglycecdise and FA to Brush Boarder

2)Enterocyte via diffusion
-Converted back to tryglycerides and globules by SER
-Globules go to Mito to become Chylomircors

3)Chylomorics move to Basolateral Side
-Move into lymph
-Lymph Ducts via cirulatory system
-Liver or adipose tissue

742
Q

Fatty acids are combined with what for blood transport?

743
Q

Triglycerides are transported as?

A

Lipoproteins

744
Q

Nutrients enters the liver through?

A

Hepatic Portal Vein

745
Q

Oxygenated blood enters the liver through?

A

Hepatic Arteries

746
Q

What are the 9 roles of the liver?

A

Blood:
1)Blood Storage
2)Blood Filtration
3)Erythrocyte Destruction

Fed/Unfed State:
4)Carb Metabolism
5)Protein Metabolism
6)Fat Metabolism

Storage
7)Vitamin Storage
8)Glycogen Storage

9)Detoxification of Chemicals

747
Q

What is the role of the kidney?x4

A

1)Regulates salt and water concentration in the blood through the formation of urine

2)Blood Pressure Regulation

3)Osmoregulation

4)Acid-Base Homeostasis

748
Q

What is a nephron

A

Filteration units of the kidneys

749
Q

What are the 3 regions of the kidney

A

1)Cortex (outer)
2)Medulla (middle)
3) Pelvis (Fluid ext. for urine)

750
Q

Where does blood first enter the kidney

A

Bowman’s capsule, no selective only small particles through (NOT BLOOD)

751
Q

A single nephrons spans what parts of kidney?

A

Cortex and Medulla

752
Q

Path of flitration in nephron

A

1)Bowmans Capsule
2)Glomerulus
3)Proximal Convoluted Tubule
4)Descending Loop of Henle
5)Ascending Loop of Henle
6)Distal Confuloted Tubule
7)Collecting Duct

753
Q

Path of Filtration in Kidney

A

1)Blood Enters through renal artery which divides into afferent arterioles that branch into capillarilies called glomerulus

2)Efferent Arterioles which divides into Vasa Recta

3)Vasa Recta surrounds nephron

4)
-Converge into renal vein which heads back into ciruclation
-Urine collects from collecting ducts and exits kidney through urter

754
Q

Increasing blood into the afferent arteriole (kidney) does what to BP

A

Increase BP

755
Q

What is the role of angiotension 2

A

Vasconsticts the efferent arteriole
Increase Gobular Filtrartion Rate

756
Q

Angiotension 2 effect on BP

A

Increase BP

757
Q

What are the names of the two types of nephrons

A

Cortical Nephron (small)

Justamedullary Nephrone (Longer)

758
Q

What neurons is associated with urine concentratrion

A

ustamedullary Nephrone (Longer)

759
Q

What are the 3 processes of kidney

A

1)Filtration : No selective

2)Secretion: Selective

3)Reabsorption: Selective
-essential substances are reabsoptied from filtrate rb

760
Q

Compare the sizes of the afferent arteriole and efferent arteriole

A

Afferent is large the efferent creating a hydrostatic pressure

761
Q

True or False Osmolarity stays the same from the start filtrate to end filtrate

A

True
only a decrease in volume of filtrate is obeserve

762
Q

What occurs in the proximal tubule

A

Secretion and Reabsorption

763
Q

What occurs in the decending loop

A

H2O Flows out

(fluid is highly concentrated, so wants out)

764
Q

What occurs in the ascending loop

A

NaCl Flows Out

765
Q

What occurs in distal tubule

A

Further fine tuning of secretion and reabsoprtion

766
Q

Osmotic Concentration increases up or down loop

767
Q

What is the function of the loop of henle

A

Increases the intersitial (medulla) salyt concentration (salt out of filtrate) w/out significant changing solute concentration of filtrate

768
Q

Distal Convulated tubule role in RAAS

A

JGA connects to arterioles of glomerus to distal convulted tubule

-JGA sense changes in solute concentration in DCT and detects streching arteriole wall

-If low Na+ GA cell srelease Renin, causing release of Aldosterome

769
Q

Aldosterone role in kidney

A

Increases Na+ Reabsorption in DCT and collecting duct

Increases blood osmolarity, volume and pressure

-Stiulates ADH release and thirst

770
Q

The collecting duct in impermeable to water expect when?

A

WHhen Ant-Diuertic Hormone is released, water passes out into medulla

771
Q

True or False water should be in urine

A

False, nutrient in ducts and descending

772
Q

What hold Ca in muscle cell

A

Sacoplasmic Ret. (SR)

773
Q

What are the 3 steps of AP

A

1)Na+ channels open (+ charge enters cell) -DEPOLARIZATION

2)K+ channel opens (+) charge exits cell to extracellular space -REPOLARIZATION

3)Re-Establish normal membrane potential (Na+/K+ ATPase)

774
Q

What is constantly working in a cell regardless of AP

A

Na+K+ ATPase

Na in
K out

775
Q

AP causes what to enter the cell

776
Q

What does Ca+ in cell result in for ATP

A

Vesicles fill wit Ach
-Ach released into synaptic cleft by exocytosis

777
Q

What are groves in plasma membrane of muscle cell called

778
Q

What is the sacrolma

A

Muscle Membrane

779
Q

Ach receptors on muscle membrane are also receptors for what?

A

Na+
Therefore you can have AP in Sacrolma

780
Q

What causes the SR to release Ca to allow for muscle contraction?

A

AP travels down T-Tubules from pre-synaptic celll

781
Q

3 Types of Muscle

A

1)Cardiac
2)Smooth
3)Skeletal

782
Q

3 Functions of Muscles

A

1)Body Movement and Support
2)Movement of substances throughout body
3)Thermoregulation

783
Q

Tendons

A

Muscle to Bone

784
Q

Ligaments

A

Bone to Bone

785
Q

Skeletal Muscle is conscious or unconscious control?

A

Concious and Voluntary

786
Q

When a muscle contracts it moves towards what point

A

Insertion pt to Origin Point

787
Q

The antagonist muscle vs agonist muscle

A

Agonist is the one that contracts
(flexors)
Antagonist is the one that relaxes(extensors)

788
Q

What is a first class lever
-Effort
-Fulcrum
-Resistance

A

Effort=one side down
Fulcrum= Middle
Resistance= opposite side of effort dip

789
Q

What is a second class lever
-Effort
-Fulcrum
-Resistance

A

-Effort: Up on one side
-Fulcrum =Oppposide side effort
-Resistance= middle down

790
Q

What is a third class lever
-Effort
-Fulcrum
-Resistance

A

-Effort: Middle Up
-Fulcrum: One side
-Resistance: Opposide to fulcrum down

791
Q

How can muscle contraction be unconsious (ans)

A

-Contraction can squeeze blood in ciruclatory system
-Move metabolites away

-Shivering to make warm

792
Q

What is the sacromere

A

Myosin (Thick Fil)
Actin (Thin Fil)

793
Q

What does contraction look like in the sacromere

A

Myosin filaments force actin to move closer together pulling Z-Band closer together.

(MORE OVERLAP CONTRACTING)

794
Q

A-Band

A

All Mysosin

No change regardless of overlap

795
Q

I- Band

A

Actin Only
Decreases with Contraction (more overlap)
Increases with Relax (less overlap)

796
Q

H Zone

A

Myosin Only
Decreases with Contraction (more overlap)
Increases with Relax (less overlap)

797
Q

Z Band

A

Boarders of sacromere units

798
Q

M Line

A

In A-Line
-Closest distance that two acton filaments can be realtive to one another la

799
Q

What part of the muscle has a straiated apperance

A

Sacromers
-Sacromers positioned end to end form a myofibril (gives the apperance)

800
Q

True or False the Skelteal Muscle cells have lots of mitochrondiea

A

True lots of mito and nuclei

801
Q

What are myobrils?

A

Several Sacromeres attached together

-Many myofribris in a muscle

802
Q

6 Steps of Muscle Contraction:

A

1)Motor neuron (somatic Nervous system) depolarizes, AP

2) At end of motor neuron Ca2+ channels open, ACH is released by excoytosis into synaptic cleft, binds muscle ACH receptors , Open Na+ channels in muscle (AP)

3)New AP travels along sacrolema, down T-Tbules and trigger Ca2+ relase from SR

3)Ca binds tropnin whic shoft tropomyosin

4)Mysosin binds ATP, release any previous actin bidning, hyrdolyzes ATP and extend out binds actin and pull actin back in for muscle contraction

5)Resets for next signal: gather Ca+ back into SR (Ca ATPASE) wait for next AP

803
Q

What is the role of troponin?

A

Shifts off tropomyosin

804
Q

What is the role of tropomysosin?

A

Blocks actin and myosin from binding
-Covers active site on Actin

805
Q

Steps of Contraction in terms of myosin and actin?

A
  1. Ca+ binds troponin
  2. Tropnin moves tropomyosin off actin revealing active site
  3. Mysosin binds ATP (releases actin) (low energy)
  4. Mysosin Hydrolyzes ATP (ADP =Pi) (high energy)
  5. Mysosin binds actin (froming cross bridges)

6) Releases PI + ADP for powers stroke
-Mysosin back to low enegry
-Actin pulls towards center

7) New ATP Added, releases Actin (start again)

806
Q

What happens if no new ATP is avaliable for myson to bind

A

Stuck contracted to suck to mysosin
Rigormortis

807
Q

What are the 2 ways skeletal muscle becomes fatigued

A

1) Nervous (not enough ACH)
2)Metabolic (Not enough ATP)

808
Q

What is Oxygen Debt

A

The increased need for oxygen after exercise after exercise in order to metobilize the byproducts of anaerobic glycolysis (lactic acid()

809
Q

3 types of skeletal muscle fibres

A

1)Type 1: Slow Twich/Slow Oxidative

2)Type 2A: Fast Twitch/ Fast Oxidative

3)Type 2B: Slow Twitch/ Fast Glyolytic

810
Q

What skeletal muscle types are red

A

Type 1
Type 2 A

High amounts of myoglobin

811
Q

Why are Type 2B muscles white

A

Low Myogolbin

812
Q

What muscle fibre type has the most amount of mitochondria

A

Type 1 (can be used for ling oeriods of time )

813
Q

Type 1 Muscle
-Contraction Time
-Force Production
-Resistance to Fatigue
-Activity

A

-Contraction Time : SLOW

-Force Production: LOW

-Resistance to Fatigue: HIGH

-Activity: OXIDATIVE

814
Q

Type 2A Muscle
-Contraction Time
-Force Production
-Resistance to Fatigue
-Activity

A

-Contraction Time: FAST

-Force Production: HIGH

-Resistance to Fatigue: Intermediate

-Activity: Longterm Anerobic

815
Q

Type 2B Muscle
-Contraction Time
-Force Production
-Resistance to Fatigue
-Activity

A

-Contraction Time : VERY FAST

-Force Production: VERY HIGH

-Resistance to Fatigue: VERY LOW

-Activity: SHORT TERM ANAROBIC

816
Q

What is a Motor Unit

A

A group of muscle cells sharing one motor nerve

817
Q

How is AP different in Cardiac Muscle

A

PLATEAU Slow Repolarization

Prevnts Teatanus

818
Q

SKELETAL MUSCLE CELL
-Control
-Striations
-Nucleus
-Shape

A

-Control: VOLUNTARY

-Striations: YES

-Nucleus: MULTI

-Shape : NON-BRANCHED (MYOFRIBRILS)

819
Q

CARDIAC MUSCLE CELL
-Control
-Striations
-Nucleus
-Shape

A

-Control: INVOLUNTARY

-Striations: YES

-Nucleus: 1

-Shape : BRANCHED

820
Q

SMOOTH MUSCLE CELLS
-Control
-Striations
-Nucleus
-Shape

A

-Control: INVOLUNTARY

-Striations: NO

-Nucleus: 1

-Shape :TAPERED

821
Q

How many bones in human body

822
Q

4 fxns of bones

A

1)Structural Intergity and Support
2)Stores Ca
3)Protection for Ograns
4)Large bones shelter bone marrow, containes adipose tissue and stem cells

823
Q

Bone is important for regulating

A

Ca and Phosphate
Site of blood cell formation

824
Q

Long bones house what 2 things

A

Yellow Marrow (fats)
Red Marrow (site of RBC development)

825
Q

Flat bones house what

A

Red Bone Marrow (site of RBC developement)

826
Q

Osteoprogenitor Cells

A

Differentate into osteoblasts

Osteoblats –> Osteocytes

827
Q

Osteoclasts

A

Derive from white blood cells
-Hemopoetic Stem Cells

-Release Ca+ into Blood (PTH)

828
Q

Osteoblasts

A

Form bone
Calictonin

829
Q

What are osteocytes used for

A

Exchange wastes and nutrients with the blood

830
Q

Role of Calictonin

A

Decreases osteoclast

831
Q

True or False Bone Cells undergo mitosis

832
Q

Spongy bond has what type of none marrow

A

Red Bone Marrow

833
Q

Compact bone has what type of bone marrow

A

Yellow Bone Marrow

834
Q

At birth what type is all bone marrow

835
Q

What 3 Cells arise in red blood marrow

A

1)Red Blood CElls
2)White Blood CElls
3)Platelets

836
Q

What is the periosteum of the bone responisble for?

A

Fibrous sheath that surrounds the long bone and is the site of attachement of muscle tissue

837
Q

What occurs at the epiphyseal plate?

A

Growth plate
-Stopped growing = Epiphyseal line

838
Q

What is the Haversian Suystem

A

Structucted and Highly Vascularized organization of compact bone

839
Q

What makes Haversian Canals

A

Osteoclasts

840
Q

How are lamellae formed in bones

A

Osteoblasts following haversian canals and lay done new matrix on tunnel walls

841
Q

How do osteocytes exchange wastes in haversian system

A

Canaliculi

842
Q

What are Volkmnann’s Canals

A

Cross links haversian canals

843
Q

What are the 2 things a osteon is made of?

A

1)Lamallae
2)Haversion Canal

844
Q

What do lacuna contain

A

Osteocytes

845
Q

What is cartilage

A

Flexiable tissue found in joints between bones, ribcage, ear and nose

846
Q

Why does cartilage heal slowly

A

No blood vessels

847
Q

What are the 3 types of cartilage and which is the most common?

A

1)Hyaline (most comon reduce friction and shock btwn joints)
2)Fibrocartilage
3)Elastic

848
Q

What are Fibrous Joints

A

Holds 2 bones tightly together , allowing for little movements

849
Q

What are cartilaginous joints

A

Allow little to no movement btwn 2 bones tightly connected by cartilage

850
Q

What are Synovial Joints

A

Do not connect bone by cartilae and are instead seperated by a capsule filled with synovial fluid

-Wide range of motopm

851
Q

True or False women have less bone density

A

True Menopause

852
Q

3 General Functions of Skin

A
  1. Heat Homeostasis
  2. Water Homeostasis
  3. Osmoregulation
853
Q

3 Layers of Skin

A

1)Epidermis
2)Dermis
3)Hypodermis

854
Q

What is the epidermis consist of

A

Stratified Squamous Epithelial Cells (Keratinocytes)

855
Q

3 Specialized Cells of Epidermis?

A
  1. Ketinocytes (produce keratin, dominate)
  2. MelanocytesL produce Melanin
  3. Dendritic Cells: Pagocytes
856
Q

Layers of Epidermis (superficial to deep)

Come, Lets Get Sun Burnt

A

Corneum
Lucidum
Granulosum
Spinosum
Basale

857
Q

What is the dermis

A

Connective Tissue and Procides blood, nutrients and neurons to the epidermis

Fibroblasts
Hair Follciles
Blood Vessels and Nerves

858
Q

Hypodermis

A

Subcutaneous Tissue
Adipose

Absorbs shock and provides insuation

859
Q

At resting potential there is more Na+ inside or outside of cell

A

Oustide

Resting mebrane potential is -70 mV

860
Q

Excitory do what?

A

Depolarize (making more positive)

861
Q

Inhibitory do what?

A

Polarize (making more negative)

862
Q

The CNS can be characterized as what?

A

Brain and Spinal Cord

863
Q

Dendrites

A

Receieve a signal to be transmitted

-Where graded potentials start

864
Q

Cell Body (Soma)

A

Where graded potentials build to trigger ATP

865
Q

Axon Hillock

A

Generates a outgoing AP

866
Q

Axon

A

Transmits the outgoing AP

867
Q

AP jumps between what

A

Nodes of Ranvier

Between Swann cells

868
Q

What is satatory conduction

A

AP jumping between nodes ranvier increasing transmission speed

869
Q

What do swann cells do

A

Make Mylein

870
Q

How does myelin afect AP

A

Increases the rate at which an acon can transmit AP by insulating it

871
Q

White Matter v Grey Matter in Axons

A

Myelinated Axons are WHite
Dell Bodies are Grey

872
Q

What 2 things produce Myelin

A

Schwann Cells PNS
Oligodendrocytes CNS

873
Q

Na+/K+ ATPase moves how many Na+ in and K+ out

A

3 Na+ IN
2 K+ OUT

874
Q

How do neurotransmitters diffuse across synaptic cleft (pre to post)

A

Brownian (random diffusion)

874
Q

Where do electrical synapses exist

A

Cardiac cells

875
Q

WHat happens if a neurone is fired to many times

A

Fatigue
-Can also be degrated by enzymes

876
Q

True of False Neurotransmitters always excite post synaptic cell

A

False can also inhibit

877
Q

How do local anestethics work

A

Block voltage gated Na+ Channels on nerves to prevent pain transmission

878
Q

How many nodes of Ranvier need to be blocked to block a nevre

A

3 Consecutive

879
Q

What is threshold potential

880
Q

Spatial Summation

A

Multiple dendrites recieve input at the SAME time and those inputs are summed up

881
Q

Temproal Summation

A

Single densrie reveives informaion in succesion and those inputs are summed up

882
Q

What are Glial Cells/Neurogila

A

Cells which support the nervous system

883
Q

6 Types of Glial Cells

A

CNS
1)Ependymal Cells: Conatin CSF epitheial cells
2)Oligodendrocytes: Myelin
3)Astrocytes: Shape and physical support
4)Microglia : Macrophage of CNS

PNS
5)Satellite Cells: Support
6)Schwann: Mysosin

884
Q

Somatic versus Autonmic parts of PNS

A

SOmatic: Skeletal Voluntary

Autonomic: Everuthing else Involuntary

885
Q

Sympatetic Neuron pathway

A

Pre-Synaptic Neuron
Short-Axon (Ach Released)
Post Synaptic Neuron
Long Axon (Norepi released)
Target

886
Q

Parasympatehtic Pathwayhe

A

Pre-Synaptic Neuron
Long Axon (Ach)
Post-Snaptci Neuron
Short Axon (ach)
Target

887
Q

What are the 3 types of neurons in the nervous system

A

1)Sensory (afferent) Neurons (Back- Dorsal)
2)Interneurons
3)Motor Neurons (Front -Ventral)

888
Q

What are 90% of neurons in the body

A

Interneurons

889
Q

3 Components of the Brainstem

A

1)Midbrain
2)Pons
3)Medulla

890
Q

Midbrain

A

Relay station for auditory/visual info

891
Q

Pons

A

Facilitate transfer of motor info from motor cortex –> cerebellum

892
Q

Medulla

A

Regulate cardiovasulcar and respiratory system (BP)

893
Q

Cerebellum has what role

A

Coordinates and Plans Movemnt

Gyri and Sulci (folded neuronal tissue)

894
Q

4 Lobes of Cerebral Cortex

A

1)Frontal Lobe
2) Parietal Lobe
3)Temporal Lobe
4)Occipital Lobe

895
Q

Frontal Lobe

A

Higher Exec. Function
Motor Cortex for Voluntary Fxn

896
Q

Parietal Lobe

A

Somatosensory Cortex
-Detect touch, pain and temp

897
Q

Temporal Lobe

A

Integration of auditory and olfactory info

BAR

898
Q

Occipital Lobe

A

Process visual inputs

899
Q

Reflex are apart of what nervous system

A

Somatic (voluntary) system of PNS
SEEMS ODD JUST REMEBER

900
Q

ANS is antagonist or agonist

A

Antagonist

901
Q

The Vagus nerve is apart of what system

902
Q

Sympathetic Nervous system comes from what part of spinal cord

A

Middle
Thoracic and Lumbar

903
Q

Parasynpathetic Nervous system comes from what part of spinal cord

A

Top/Bottom
Cervical and Thoracic

904
Q

What is the post synaptic neurostransmitter for Sympathetic

A

Epinenephrine and NORephinrine
(ADRENALINE from adrenal medulla)

905
Q

Pathway of somatic motor neuron

A

Somatic motor neuron: Voluntary of PNS
ACH
Effector

MUSCLES

906
Q

What is the effect of vitamin D on ca

A

Increase Ca Reabsorbtion