Biology Flashcards

1
Q

what happens in the nucleolus?

what does an endosome do?

A

rRNA is synthesized

endosomes transport/package/sort cell material traveling to/from the membrane
- involved in endocytosis

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2
Q

what is the function of the endoplasmic reticulum?
compare smooth vs rough ER

what about the golgi?

what about peroxisomes?

A

ER function is synthesis/transport of biomolecules
Smooth does lipid synthesis, Rough does protein synthesis

The golgi modifies then packages/transports cellular products to their correct destination

peroxisomes do B-oxidation, synthesis of phospholipids, have enzymes for PPP

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3
Q

describe the 3 components of the cytoskeleton

  1. microfilaments
  2. MTs
  3. intermediate filaments
A
  1. Microfilaments are made of actin, and give the cell protection; also form a ring during cytokinesis of mitosis
  2. MTs are made of tubulin, providing pathways for kinesin/dynein (motor proteins) to carry vesicles; also cilia and flagella
  3. Intermediate filaments do cell-cell adhesion and maintain integrity of cytoskeleton
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4
Q

explain types of epithelial cells:

  • simple
  • stratified
  • pseudostratified
  • cuboidal
  • columnar
  • squamous
A
  • simple - one layer of cells
  • stratified - multiple layers of cells
  • pseudostratified - one layer but appear as multiple
  • cuboidal - cube shaped
  • columnar - long and thin
  • squamous - flat/scalelike
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5
Q

gram-positive vs. gram-negative cell walls

A
  • gram-positive has a thick layer of peptidoglycan (protection from host’s immune system) and also contains lipoteichoic acid
  • gram-negative contain small amount of peptidoglycan and also outer membranes containing lipopolysaccharides
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6
Q

what is binary fission?

what are virulence factors?

A

asexual reproduction in prokaryotes

they’re traits that increase pathogenicity (toxin production/projections/evasion)

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7
Q

transformation vs. conjugation vs. transduction for bacteria

A

Transformation is integration of foreign material into the host genome. Conjugation is bacterial form of mating (forming conjugation bridge, donor male + to recipient female - . Transduction genetic recombination process that requires a vector

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8
Q

what is a transposon

what are the phases of bacteria growth?

  • lag phase
  • exponential/log phase
  • stationary phase
  • death phase
A

genetic elements capable of inserting and removing themselves from the genome

  • lag phase is when bacteria first adapt to the new local conditions
  • exponential/log phase is when rate of division increases
  • stationary phase is when reduction of resources slows reproduction
  • death phase is when environment cant support bacteria and they die
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9
Q

what is a capsid? what are virions? what are bacteriophages? describe functions of tail sheath vs tail fibers

A

capsid is the protein coat of a virus. virions are viral progeny used to infect other cells. bacteriophages are viruses that target other bacteria. tail sheath acts like a syringe, tail fibers recognize/connect to correct host cell

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10
Q

what is a retrovirus? describe positive vs. negative sense genomes

A

retroviruses are ssRNA viruses that carry reverse transcriptase, synthesizing DNA from RNA and integrating that DNA into the host cell’s genome

  • positive means the genome may be directly translated from to functional proteins by the ribosomes like mRNA
  • negative carry RNA replicase to synthesize proteins from the RNA
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11
Q

lytic vs lysogenic cycles

prions vs. viroids

A

lytic cycle is when bacteriophage maximizes use of cell’s machinery w/ little regard for survival of host cell (virus is VIRULENT), lysogenic phase is when virus replicates as bacterium reproduces because it is part of host’s genome

  • prions are nonliving infectious proteins, causing misfolding of other proteins, viroids are small pathogens consistent of a very short circular ssRNA, they bind to large # of RNA seq. and silence genes in plant genome
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12
Q

the stages of the cell cycle:
G0
Interphase - G1, S, G2
M stage - Mitosis

A
  • G0 - cell is simply living / carrying out functions
  • G1 - cells create organelles for energy/protein production (RESTRICTION POINT)
  • S - cell replicates genetic material so daughter cells have identical copies (PLOIDY DOESNT CHANGE)
  • G2 - cell passes through another quality control
  • M - cells separate into identical daughter cells
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13
Q

explain p53’s role

explain role of cyclins and CDKs

A

p53 controls if cell needs to arrest to repair DNA or if it is ready for synthesis
- CDKs are activated by the right cyclins, and this complex phosphorylates TFs that promote transcription of genes for next stage of cell cycle

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14
Q

explain 4 steps of mitosis and cytokinesis

  • prophase
  • metaphase
  • anaphase
  • telophase
  • cytokinesis
A
  • prophase - chromosomes condense, centrioles separate to poles and spindle fibers form
  • metaphase - chromosomes align at metaphase plate b/c of spindle apparatus
  • anaphase - sister chromatids are pulled apart by shortening kinetochore fibers
  • telophase - new nuclear membrane forms around each set of chromosomes, spindles disappear
  • cytokinesis - separation of cytoplasm and organelles to each daughter cell
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15
Q

Meiosis I and then Meiosis II

when does crossing over occur in meiosis?

A

Meiosis I results in homologous chromosomes being separated generating HAPLOID daughter cells (reductional division)
Meiosis II is similar to mitosis, resulting in separation of sister chromatids W/O change in ploidy (equational division)

Prophase I

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16
Q

what are the functions of seminiferous tubules and interstitial cells of Leydig

what do cowper’s glands do?

A

seminiferous tubules (secrete testosterone) and interstitial cells of Leydig (produce sperm)

produce clear/viscous fluid that cleans remnants of urine and lubricates urethra during arousal

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17
Q

define terms:

  • spermatogonia
  • primary spermatocyte
  • secondary spermatocyte
  • spermatid
  • spermatozoa
A
  • spermatogonia - diploid stem cells in males
  • primary spermatocyte - diploid sperm after S stage
  • secondary spermatocyte - haploid sperm after Meiosis I
  • spermatid - haploid sperm after meiosis II
  • spermatozoa - mature sperm
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18
Q

where is an egg ovulated into? and then what does it travel through? what is its destination?

A

peritoneal sac; fallopian tubes, uterus

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19
Q

define terms:

  • primary oocyte
  • secondary oocyte
  • zone pellucida
  • corona radiata
A
  • primary oocyte - created and stored until menarche, when one is released per month
  • secondary oocyte - primary oocyte after meiosis I
  • zone pellucida - surrounds oocyte, is an acellular mixture that protects oocyte
  • corona radiata - layer of cells that adhere to oocyte during ovulation
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20
Q

when does GnRH get released? what happens after that?

A

at the start of puberty the hypothalamus releases pulses of GnRH
- triggers anterior pituitary to release FSH and LH

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21
Q

describe menstrual cycle

  • follicular phase
  • ovulation
  • luteal phase
  • menstruation
  • pregnancy
  • menopause
A
  • follicular phase - begins w/ menstrual flow, GnRH increases which increases FSH and LH and produce follicles, which have negative feedback on hormones; estrogen spikes late
  • ovulation - high estrogen levels cause GnRH, FSH, LH to spike. LH surge induces ovulation
  • luteal phase - LH causes ruptured follicle to form corpus luteum which secretes more and more progesterone. negative feedback on GnRH, FSH, LH.
  • menstruation - w/o implantation, corpus luteum loses stimulation from LH, progesterone decreases, uterine lining is shed. GnRH block is removed
  • pregnancy - if implantation occurred, zygote forms into blastocyst which implants into uterine wall and secretes hCG, which maintains corpus luteum.
  • menopause - w/ age, ovarian atrophy occurs. estrogen/progesterone drop, endometrium atrophies, menstruation stops. blood levels of FSH and LH rise b/c negative feedback stops
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22
Q

determinate vs indeterminate cleavage

describe blastulation

A

determinate is when cells’ fates are already determined, indeterminate is when cells can still develop into complete organisms

  • blastulation is when morula (ball of cells) forms into a blastula (hollow ball of cells w/ fluid inside called blastocoel). mammalian blastula is a blastocyst
  • outer layer trophoblast cells become placenta, inner cell mass becomes organism
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23
Q

what is gastrulation? deuterostomes vs protostomes; describe the 3 primary germ layers

  • ectoderm
  • mesoderm
  • endoderm
A

gastrulation is generation of three distinct cell layers

  • deuterostomes develops into anus, protostomes develops into mouth
  • ectoderm - outermost layer, gives rise to hair/skin/nails/eye lens/NS
  • mesoderm - middle layer, gives rise to musculoskeletal, circulatory, excretory systems
  • endoderm - innermost layer, forms epithelial linings of organs, lungs, liver, pancreas
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24
Q

how do cells differentiate into distinct cell types during development? also talk about induction

explain neurulation

  • notochord
  • neural folds
  • neural groove
  • neural tube
  • neural crest cells
A

selective transcription of genome

  • induction is one group of cells influencing fate of nearby cells
  • chemical substances (inducers) diffuse from organizing cells to responsive cells
  • notochord - rod of mesodermal cells that forms long axis of organism (spine)
  • neural folds - notochord induces cells to slide inward forming folds, which surround neural GROOVE
  • neural tube - folds grow towards each other and fuse to form neural tube, becoming CNS
  • neural crest cells - at tip of each fold, these cells move outward to form PNS
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25
Q

rank the potency of a cell

autocrine vs paracrine vs juxtacrine vs endocrine

A
  • totipotent is greatest potency (stem cells) and can differentiate into anything
  • pluripotent can differentiate into any type except for placental structures
  • multipoint can differentiate into multiple cell types within a particular group

autocrine is to itself, paracrine is to cells that are close, juxtacrine is stimulating receptors of adjacent, endocrine is to cells far away

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26
Q

how are the umbilical arteries/vein different?

describe the 3 shunts in a fetus

  • foramen ovale
  • ductus arteriosus
  • ductus venosus
A

umbilical artery carries deoxygenated blood away from from fetus to placenta, and umbilical vein carries oxygenated blood and nutrients to fetus from placenta

  • foramen oval is one way valve connecting R atrium to L atrium, avoiding ventricles and driving blood in circulation
  • ductus arteriosus - shunts leftover blood from pulmonary artery to aorta
  • ductus venosus - shunts blood returning from placenta directly into inferior vena cava
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27
Q

what happens in first trimester? second trimester? third trimester?

talk about birth

  • parturition
  • prostaglandins
  • oxytocin
  • afterbirth
A

1st trimester is when major organs begin to develop, skeleton begins to form into bone, brain fairly developed
2nd trimester fetus undergoes tremendous growth, begins to move, face becomes human, toes/fingers elongate
3rd trimester is more growth and brain development, antibodies transferred from mother,

  • parturition - vaginal childbirth
  • prostaglandins - coordinates rhythmic contractions of uterine muscle
  • oxytocin - peptide hormone in pos. feedback for contractions
  • afterbirth - placenta and umbilical cord are expelled
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28
Q

what cells produce myelin? (in PNS and CNS)
- difference b/w tracts and nerves?

temporal vs. spatial summation

A

oligodendrocytes in CNS and schwann cells in PNS
- nerves carry more than one type of info, tracts only carry one

temporal is multiple signals integrated during a short period of time, spatial is additive effects based on # and location of incoming signals

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29
Q

define the function of each:

  • glial cells
  • astrocytes
  • ependymal cells
  • microglia
  • oligodendrocytes (CNS) / schwann cells (PNS)

what is saltatory conduction?

A
  • glial cells - myelinate neurons
  • astrocytes - form BBB
  • ependymal cells - line ventricles of brain, produce CSF
  • microglia - ingest/break down waste products in CNS
  • oligodendrocytes (CNS) / schwann cells (PNS) - produce myelin for axons

the signals hops from node to node

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30
Q

what part of the spinal cord are sensory neurons found?

what is the first neuron in ANS called? second neuron?

A

dorsal root ganglia

preganglionic neuron; postganglionic neuron

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31
Q

difference in function b/w peptide hormones and steroid hormones

  • what do peptide hormones end in? steroid hormones?
A

peptide hormones can’t pass membrane so they use second messenger, steroid hormones diffuse thru membrane so they bind to intracellular receptors (slower effect)

-in or -ine; -one or -oid

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32
Q

direct vs. tropic hormones

products of anterior pituitary mnemonic? which are tropic and which are direct?

A

direct hormones act directly on target tissue, tropic hormones require an intermediary to act

F - FSH
L - LH
A - ACTH 
T - TSH
Prolactin
Endorphins
G - GH
FLAT is tropic and PEG is direct
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33
Q

where does the hypothalamus secrete compounds? what does being hormones to?

what is the HPA axis? how does negative feedback work for it?

A

hypophyseal portal system; anterior pituitary

hypothalamus->CRF->anterior pituitary->ACTH->adrenal cortex->cortisol
- cortisol inhibits ACTH and CRF when too high

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34
Q

define the function of the following:

  • ADH (vasopressin)
  • oxytocin
  • prolactin

contrast anterior vs posterior pituitary

A
  • ADH (vasopressin) - increases reabsorption of H2O in ducts of kidneys
  • oxytocin - stimulates uterine contractions
  • prolactin - stimulates milk production in mammary glands

anterior produces/secretes its own hormones, posterior is projection of hypothalamus and stores/secretes those hormones

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35
Q

what are the 2 functions of the thyroid?

how does it mediate both effects?

A
  1. setting BMR
  2. promoting Ca2+ homeostasis
  3. releases T3 & T4, which increases cell. resp.
  4. release of calcitonin, which decreases plasma Ca2+ levels
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36
Q

what does parathyroid hormone (PTH) do?

what is the 3 functions of corticosteroids mnemonic?

A

serves as an antagonistic hormone that raises blood Ca2+ levels
- also activates vit.D which is required for Ca2+ absorption

3 S’s

  • Sugar (glucocorticoids)
  • Salt (mineralocorticoids)
  • Sex (cortical sex hormones)
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37
Q

define functions of each corticosteroid, which are released by the _____

  1. Glucocorticoids
  2. Mineralocorticoids (describe how low BP is regulated)
  3. cortical sex hormones
A

adrenal cortex

  1. Glucocorticoids - regulate BGL, affect protein metabolism; Cortisol and Cortisone decrease inflammation
  2. Mineralocorticoids - used in salt/water homeostasis (aldosterone)
    - low BP causes juxtaglomerular cells to secrete renin, which cleaves angiotensinogen to angiotensin I, then to angiotensin II by ACE. angiotensin II bring BP up
  3. cortical sex hormones release androgens/estrogens
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38
Q

what are the 3 types of Islets of Langerhans in the pancreas? what does each one secrete?

compare Type I vs Type II diabetes

what does somatostatin do?

A
  1. alpha - glucagon
  2. beta - insulin
  3. delta - somatostatin

Type I is caused by destruction of B-cells, so low/no insulin production. Type II is result of receptor resistance to effects of insulin

inhibits glucagon and insulin secretion, also GH secretion

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39
Q

what does erythropoietin do and where is it secreted from?

talk about atrial natriuretic peptide (ANP)

also thymosin

what secretes melatonin?

A

from the kidneys
- stimulates bone marrow to increase production of erythrocytes in response to low blood O2 levels

released from heart to regulate salt/water balance

thymosin is released from thymus which is important for T-cell development/differentiation

pineal gland

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40
Q

order that air goes from mouth to lungs

define the following terms:

  • total lung capacity (TLC)
  • residual volume (RV)
  • vital capacity (VC)
  • TV
  • expiratory reserve volume (ERV)
  • inspiratory reserve volume (IRV)
A

mouth to pharynx to larynx to trachea to bronchi to bronchioles to alveoli

  • total lung capacity (TLC) - max lung volume when inhaling completely
  • residual volume (RV) - volume remaining after exhalation
  • vital capacity (VC) - TLC-RV
  • TV - volume inhaled/exhaled during normal breaths
  • expiratory reserve volume (ERV) - volume of additional air that can be exhaled
  • inspiratory reserve volume (IRV) - volume of additional air that can be inhaled
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41
Q

what enzyme is in the nasal cavity? describe mucociliary escalator

what 3 immune cells are in the lungs?

what is the bicarbonate buffer system equation?

A

lysozyme; mucus catches particles/large matter, then cilia propel mucus up respiratory tract to be expelled/swallowed

  1. macrophages
  2. IgA antibodies
  3. Mast cells

CO2 + H2O -> H2CO3 -> H+ + HCO3-

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42
Q

what do each of these hormones cause to release form the anterior pituitary?

  • GnRH
  • GHRH
  • TRH
  • CRF
A
  • GnRH -> FSH and LH
  • GHRH -> GH
  • TRH -> TSH
  • CRF -> ACTH
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43
Q

hypothyroidism vs. hyperthyroidism

what 3 hormones affect water homeostasis?

A

hypo is when thyroid hormones are secreted in insufficient amounts or not at all, hyper is when there is overstimulation of thyroid hormones

  1. ADH released from posterior pituitary increases blood volume and decreases blood osmolarity
  2. Aldosterone from adrenal cortex increases blood volume but no effect on osmolarity
  3. ANP released from heart decreases blood volume but no affect on osmolarity
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44
Q

which side is the bicuspid (mitral) valve? tricuspid?

what do semilunar valves separate?

what nerve provides parasympathetic signals?

A

bicuspid is with L atrium/ventricle; tricuspid is with R atrium/ventricle

they separate ventricles from vasculature

vagus nerve

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45
Q

systole vs. diastole

do arteries or veins have more smooth muscle?

describe structure of arteries vs. veins

A

systole is ventricular contraction & closure of AV valves; diastole is ventricle relaxation and refilling, semilunar valves are closed

ARTERIES

arteries are highly muscular and elastic and have tremendous resistance to flow, veins are thin-walled and inelastic and can accommodate larger quantities of blood
- VEINS HAVE VALVES

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46
Q

order blood travels in the body

describe the 3 portal systems blood passes through

  1. hepatic portal system
  2. hypophyseal portal system
  3. renal portal system
A

R atrium, tricuspid value, R ventricle, pulmonary valve, pulmonary artery, lungs, pulmonary venules, pulmonary veins, L atrium, mitral valve, L ventricle, aortic valve aorta, arterioles, capillaries, venules, veins, IVC/SVC, R atrium

  1. hepatic portal system - blood leaving capillary beds of gut passes through hepatic portal vein before liver
  2. hypophyseal portal system - blood leaving capillary beds in hypothalamus travel to anterior pituitary to allow for PARACRINE SECRETION
  3. renal portal system - blood leaving glomerulus travels through efferent arteriole before nephron
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47
Q

explain functions of 3 cells in blood

  1. erythrocytes
  2. leukocytes
  3. platelets

what is hematocrit?

what is hematopoiesis and the 2 main hormones?

A
  1. erythrocytes - O2 transport by hemoglobin, DONT DO oxid. phosph. for ATP, only rely on glycolysis
    - only live for 120 days until phagocytized
  2. leukocytes - WBCs, crucial part of immune system
  3. platelets (thrombocytes) - assist in clotting, made from megakaryocytes in bone marrow

hematocrit is measure of how much of blood sample consists of RBCs

hematopoiesis is blood cell production

  • erythropoietin is secreted by kidney and stimulates RBC development
  • thrombopoietin is secreted by liver/kidney and stimulates platelet development
48
Q
what are the 5 types of leukocytes? function?
Granulocytes:
1. neutrophils
2. eosinophils
3. basophils
Agranulocytes: 
1. lymphocytes
2. monocytes (macrophages)
A
  • Granulocytes: contain cytoplasmic granules that are toxic for microbes and can be released during inflammatory rxns and allergies, etc.
    1. neutrophils
    2. eosinophils
    3. basophils
  • Agranulocytes: help in specific immune response, like particular pathogens (virus/bacteria). contain a memory bank of pathogen recognition
    1. lymphocytes
    2. monocytes
49
Q

ABO vs. Rh factor antigens

what are the 4 blood types? and what are the 2 ways to express A blood? B blood?

A

ABO antigens is composed of 3 alleles for blood type
- A (or Ia) and B (Ib) alleles are CODOMINANT, if they’re both present they’ll both be expressed
- Type O (or i) blood don’t express either, RECESSIVE to A and B
Rh factor is a surface protein expressed on erythrocytes, can be Rh+, Rh- (presence/absence of D)

A, B, AB, O
Ia Ia, Ia i, Ib Ib, Ib i

50
Q

who is a universal donor? universal recipient?

explain erythroblastosis fetalis

what is CO equation? BP equation?

A

type O is universal donor, type AB is universal recipient

if fetus is Rh+ and mother is Rh-, mother is sensitized to Rh factor and makes antibodies, and next child could die because mother’s immune system fights fetal blood cells if Rh+ again

CO = SV x HR
BP = TPR x CO
51
Q

hydrostatic pressure vs. oncotic (osmotic) pressure (in blood) (STARLING FORCES)

explain coagulation; what does prothrombin form? then converted to what?

what breaks down a clot?

A
  • hydrostatic pressure is force the blood exerts against vessel walls
  • osmotic (oncotic) pressure is sucking pressure generated by solutes as they attempt to draw water into bloodstream

when endothelium of blood vessel is damaged, connective tissue containing TISSUE FACTOR is exposed, platelets detect tissue factor and it’s sensed as injury. Platelets aggregate, and coagulation factors (secreted by liver) initiate cascade.
- prothrombin is activated and forms thrombin by thromboplastin, then convert fibrinogen into fibrin, which forms net over injury

plasmin, generated by plasminogen, breaks down a clot

52
Q

innate (nonspecific) immunity vs. adaptive (specific) immunity

A
  • innate immunity is defenses that are always active against infection, but lack ability to target specific invaders
  • adaptive immunity is defenses that target specific pathogens (slower to act)
53
Q

The ____ is the location of blood storage
- what do plasma cells produce?

what is humoral immunity?

what are T cells? where are they matured? what immunity are they part of?

A

bone marrow
- antibodies (adaptive immunity)

part of adaptive immunity where antibodies dissolve in blood

T-cells are a class of adaptive immune cells, mature in thymus, agents of CELL-MEDIATED IMMUNITY (coordinate immune system and kill viral cells)

54
Q

what do lymph nodes do?

what are adenoids, tonsils, peyer’s patches, and lymphoid aggregates examples of?

A

produce/filter lymph, activate B-cells,

gut-associated lymphoid tissue (GALT)

55
Q

function of lymphocytes? monocytes?

A
  • lymphocytes produce antibodies, modulate immune system, target killing of infected cells
  • monocytes are phagocytic cells in bloodstream, become MACROPHAGES (microglia, langerhans, osteoclasts)
56
Q

what is complement system? classical vs. alternate pathway

what is an interferon? when is it produced?

A

complement system consists of # of proteins in blood that act as NONSPECIFIC defense against bacteria

  • can be activated through classical pathway (requires BINDING OF ANTIBODY to pathogen)
  • or activated through alternate pathway (DOES NOT REQUIRE ANTIBODY)

produced when a cell has been infected with viruses, it is a protein that prevents viral replication/dispersion

  • increased antigen representation
  • decreased permeability
57
Q

what does a macrophage do when it detects a bacterial invader? talk about cytokines too

describe MHC

A

it is activated

  1. phagocytizes invader thru endocytosis
  2. digests invader using enzymes
  3. presents little pieces of invader to cells using MHC
    - macrophages can release cytokines which stimulate inflammation and recruit other immune cells

MHC binds to antigen which carries it to cell surface to be recognized by adaptive immune system

58
Q

MHC-I vs. MHC-II

what is a pattern recognition receptor (PRR)?

A
  • MHC-I is in all nucleated cells in body and presents ENDOGENOUS PATHWAY b/c binds antigens from inside cell
  • MHC-II is in antigen-presenting cells (macrophages) and presents EXOGENOUS PATHWAY b/c antigens originate outside of cell

PRRs are able to recognize category of invader and allows for appropriate cytokines and then appropriate immune cells

59
Q

explain each kind of cell

  • natural killer cells (NK)
  • neutrophils
  • eosinophils
  • basophils / mast cells
A
  • natural killer cells (NK) - nonspecific lymphocyte, destroys body’s own cells that are infected (goes after cancer cells)
  • neutrophils - short lived leukocytes, phagocytic, opsonize bacteria
  • eosinophils - red/orange granules, ALLERGIC RXNS, release histamine (vasodilation & leakiness of blood vessels), causing inflammation, PARASITES
  • basophils / mast cells - purple granules, allergic responses, release histamine in response to allergens
60
Q

what is degranulation?

describe structure of antibodies

  • what is variable region?
  • what is constant region?
A

occurs when antigen binds to antibody on surface of mast cell, exocytosis of granule contents, releasing HISTAMINE

2 heavy chains and 2 light chains, held together by disulfide/noncovalent linkages

  • antigen-binding region contains variable region (domain) at tips of Y, BINDS 1 AND ONLY 1 SPECIFIC ANTIGEN
  • constant region is remaining part of Y, where macrophages/NKs/etc. bind for complement cascade
61
Q

where do naive B-cells wait? what happens when that antigen is detected? (what 2 cells are produced?

primary vs. secondary response

A

lymph nodes, waiting for their antigen to come

  • upon exposure to right antigen, B-cells proliferate producing 2 types of cells: plasma cells & memory-B cells
  • plasma cells produce large amount of antibodies
  • memory-B cells stat in lymph node, awaiting reexposure

primary response is initial activated, 7-10 days, plasma cells die but memory cells live; secondary response is if reexposure ever occurs

62
Q

positive vs. negative selection of T-cells

explain killer T-cells (CD8+)
- MHC-I or MHC-II?

A

Positive selection is allowing only maturation of cells that can respond to presentation of antigen on MHC. Negative selection is causing apoptosis in cells that are self-reactive

killer T-cells (CD8+) are capable of directly killing virally infected by injecting toxic chemicals that promote apoptosis into infected cells
- MHC-I b/c better for extracellular infections (8x1=8)

63
Q

explain helper T-cells (CD4+)

  • what does loss of these cells do?
  • MHC-I or MHC-II?
A

helper T-cells (CD4+) coordinate immune response by secreting chemicals known as lymphokines, which recruit other immune cells and increase their activity

  • loss of them (occurs in HIV) prevents immune system from mounting adequate response to infection
  • MHC-II b/c better for intracellular infections (4x2=8)
64
Q

explain suppressor T-cells

explain memory T-cells

A

suppressor T-cells express CD4, but also Foxp3.

  • these cells keep immune response in sweet spot
  • turn off self-reactive lymphocytes

memory T-cells can be generated to await reexposure

65
Q

what happens with self-antigens and autoimmunity?

active vs. passive immunity

what is hypermutation?

A

self-antigens are attacked by immune systems for people with autoimmune diseases

active immunity is when your immune system does the job of making you immune (vaccines) longer lived, passive immunity is when someone else’s immune system does the work (maternal), short lived

hypermutation is what gives an antibody specificity to an antigen

66
Q

how do lymphatic vessels provide a secondary system for circulation?

where are lacteals located? what travels through them?

what are geminal centers?

what structure is responsible for returning material from lymphatic circulation back to cardiovascular system?

A

they drain tissues to push little remaining liquid back into bloodstream

located at center of each villus in small intestine, carry chylomicrons filled w/ fat (chyle)

germinal centers are collections in lymph nodes where B-cells proliferate/mature

thoracic duct!

67
Q

what are the 2 types of helper T-cells

A
  1. T h1 cells release interferon gamma, activating macrophages and helping to kill bacteria
  2. T h2 cells activate B-cells
68
Q

what does the enteric nervous system do?

what 2 enzymes are released in saliva?

what are the 3 parts of the pharynx?

A

governs function of GI system (e.g. peristalsis)

salivary amylase (hydrolyzes starch into sugars) and lipase (catalyzes lipid hydrolysis)

oropharynx, nasopharynx, laryngopharynx

69
Q

what are the 2 esophageal sphincters? which one is associated w/ GERD?

explain the 4 divisions of the stomach

  1. fundus
  2. body
  3. antrum
  4. pylorus

lesser curvature vs. greater curvature
- what are rugae?

A

upper esophageal sphincter (muscles of oropharynx) and lower esophageal sphincter (entrance to stomach), LES is complicated w/ GERD

  1. fundus - very top section, contains mostly gastric glands
  2. body - middle part, contains mostly gastric glands
  3. antrum - second lowest part, contains mostly pyloric glands
  4. pylorus - closest to small intestine, contains mostly pyloric glands

lesser curvature is inner curve, greater curvature is outer curve
- rugae are the folds that make up lining of stomach

70
Q

what do gastric glands do? define the 3 types

  • mucous cells
  • chief cells
  • parietal cells

what about pyloric glands? (what do G-cells secrete?)
- what does gastrin do?

A

respond to signals from vagus nerve of PNS in response to sight, taste, smell of food

  1. mucous cells - produce bicarbonate rich mucus that protects muscular wall from acid (pH=2)
  2. chief cells - part of gastric juice; secrete pepsinogen (zymogen form of pepsin), which cleaves peptide bonds near aromatic AAs
  3. parietal cells - part of gastric juice; secrete HCl, cleave pepsinogen into pepsin
    - also secretes INTRINSIC FACTOR, glycoprotein involved in absorption of B12

contain G-cells that secrete gastrin, a peptide hormone
- Gastrin induces parietal cells to secrete more HCl and signals stomach to contract

71
Q

what are the 3 parts of the small intestine?

what are brush border enzymes and when are they secreted?

what are the 3 other things does duodenum secrete?

A
  1. duodenum (majority of chemical digestion)
  2. jejunum (absorption)
  3. ileum (absorption)

secreted by duodenum in the presence of chyme, they break down dimers/trimers of biomolecules into absorbable monomers

enteropeptidase which activates other digestive enzymes from accessory organs of digestion, and secretes secretin/CCK into blood

72
Q

what happens when there are undigested disaccharides in intestines?

what is the role of aminopeptidase? dipeptidase?

what does enteropeptidase activate? into what? what else does it activate?

A

it creates an osmotic effect and pulls water into stool causing diarrhea

aminopeptidase removes N-terminal AA from peptide; dipeptidase cleaves peptide bond of dipeptides to release free AAs

activates trypsinogen into trypsin; activates procarboxypeptidases A and B into active forms

73
Q

what 2 things does secretin do?

what is the role of cholecystokinin (CCK)

A
  1. causes pancreatic enzymes to be released into duodenum
  2. regulates pH of digestive tract by reducing HCl secretion from parietal cells and increasing bicarbonate secretion from pancreas

CCK is secreted in response to chyme in duodenum. It is a peptide hormone which causes release of bile & pancreatic juices
- promotes SATIETY

74
Q

what are acinar cells?
- pancreatic amylase, trypsinogen, chymotrypsinogen, carboxypeptidases A & B are all enzymes in what? activated by what?

what is the role of pancreatic lipase?

how do pancreatic ducts empty into duodenum?

A

pancreatic exocrine cells that produce bicarbonate rich pancreatic juices
- all in pancreatic juices; enteropeptidase

breaks down fats into free FAs and glycerol

major and minor duodenal papillae

75
Q

explain bile ducts in liver

explain hepatic portal vein

A

bile is produced in liver and travels down bile ducts where it is stored in gallbladder and secreted into duodenum

liver receives/processes all blood draining from abdominal portion of GI tract through hepatic portal vein, then vena cava
- takes up excess sugar for glycogen, excess fat for triacylglycerols, etc.

76
Q

what is major components of bile?

what happens if liver cannot process/excrete bilirubin?

what 2 proteins does the liver synthesize?

A

bile salts, pigments (bilirubin) from breakdown of hemoglobin, and cholesterol

jaundice

  1. albumin - protein that maintains plasma oncotic pressure; also a carrier for drugs/hormones
  2. clotting factor - used during blood coagulation
77
Q

what is the role of the gallbladder? release of CCK?

what germ layer do accessory organs of digestion originate?

where do fat-soluble vitamins (A D E K) go during digestion?

A

stores/concentrates bile thru bile ducts
- upon CCK release, gallbladder contract and pushes bile into biliary tree

ENDODERM

right into chylomicrons to enter lymphatic circulation

78
Q

explain trancellular and paracellular movement of water during digestion

describe the 3 parts of large intestine

  1. cecum (and name valve and what organ attaches)
  2. colon
  3. rectum (and 2 sphincters)
A

water moves transcellularly (across cell membrane) and paracellularly (squeeze b/w cells)

  1. cecum - an out pocketing that accepts fluids exiting the small intestine through ILEOCECAL VALVE; site of attachment for appendix
  2. colon - main function is to absorb water/salts from undigested material left over from small intestine and concentrates rest into feces
  3. rectum - storage/expulsion site for feces
    - internal (involuntary) and external (voluntary) sphincters
79
Q

what are the 2 circulatory vessels in villus?

what does ghrelin do?

A

capillaries and lacteals

promotes a sensation of hungry, increasing feeding behavior

80
Q

what are the outer and inner layers of the kidney called? what exits through the renal hilum?

what is the order of structures starting from afferent arterioles?

what is the vasa recta?

A

outermost is cortex and innermost is medulla; renal artery, vein, and ureter exit through hilum

afferent arterioles, glomeruli (bowman’s capsule), proximal convoluted tube, descending/ascending loop of henle, distal convoluted tube, collecting duct

capillary bed surrounding loop of henle that is part of efferent arterioles

81
Q

for the bladder, what is:

  • detrusor muscle
  • internal urethral sphincter
  • external urethral sphincter

what is micturition reflex?

A
  • detrusor muscle - muscular lining of bladder
  • internal urethral sphincter - smooth muscle, contracted in normal state (involuntary)
  • external urethral sphincter - skeletal muscle (voluntary)

when bladder is full, PNS tells detrusor muscle to contract and internal sphincter to relax, then individual chooses to relax external sphincter to pee

82
Q

where does blood flow during filtration in nephron?

what does the glomerulus filter out? where does that go?

when/where is urea produced?

is secretion moving solutes into blood in bowman’s capsule or not?

A

blood flows from glomerulus into bowman’s capsule because of higher hydrostatic pressure in glomerulus being higher than osmotic pressure in opp. direction

filters out large molecules like cells/proteins; goes through efferent arterioles to vasa recta

urea is produced in the liver from large amount of NH3 (sometimes from meat heavy diets), then transported to kidney for exertion

NO, anywhere besides bowman’s capsule

83
Q

what is absorbed at the proximal convoluted tube (PCT)? what waste products (mnemonic)

what happens to filtrate at descending loop of henle? ascending?

what is the diluting segment of loop of henle? why are cells bigger?

is there a net increase or decrease of dilution in loop of henle? of volume?

A

AAs, glucose, vitamins, salts are reabsorbed into interstitium then vasa recta
- DUMP the HUNK (H+, Urea, NH3, K+)

descending is permeable ONLY TO WATER; ascending is permeable ONLY to SALTS

transition from inner to outer medulla, loop of Henle becomes thicker b/c cells are bigger b/c more mitochondria to move salts by active transport

slight increase in dilution, and large decrease of volume

84
Q

what does the distal convoluted tube (DCT) respond to? function? is there waste secretion or no?

what happens in collecting duct? what is it responsive to?

A

DCT responds to aldosterone, which promotes Na+ reabsorption, causing water to reabsorb w/ it and decreasing urine volume but increasing concentration
- YES waste secretion

responsive to aldosterone and ADH
- it is where water is reabsorbed, but reabsorption is dependent on permeability of duct (depending on hydration level)

85
Q

where are aldosterone and ADH secreted from? why?what effect do ADH and aldosterone have?

oncotic vs. osmotic pressure

A

Aldosterone:
- aldosterone is secreted by adrenal cortex in response to low BP
- aldosterone acts to increase Na+/K+ reabsorption by adding Na+/K+ pumps at DCT, which pulls in more water and excretes more K+, increasing BP
ADH:
- ADH (vasopressin) is released from posterior pituitary in response to high blood osmolarity
- allows more water to be reabsorbed at collecting duct (inhibited by alcohol and caffeine)

osmotic pressure is sucking pressure that draws water into vasculature by dissolved particles, oncotic pressure is osmotic pressure from dissolved proteins specifically

86
Q

layers of skin starting from outermost to innermost

what are strata? name layers from outermost to innermost (mnemonic?)

A

epidermis, dermis, hypodermic

layers of epidermis; stratum corneum, lucidum, granulosum, spinosum, basale
Come Lets Get SunBurned

87
Q

what happens in each layer of the epidermis? (

  • stratum corneum -
  • stratum lucidum
  • stratum granulosum
  • stratum spinosum -
  • stratum basale -

what does excessive keratin deposition and friction form?

A
  • stratum corneum - contains many layers of flattened keratinocytes forming barrier from pathogens
  • stratum lucidum - only present in thick hairless skin
  • stratum granulosum - site where keratinocytes die and lose their nuclei
  • stratum spinosum - site of langerhans cells, which are macrophages that present antigens to T-cells
  • stratum basale - contains stem cells and responsible for proliferation of keratinocytes (produce keratin)

CALLUSES

88
Q

what do melanocytes derive from? where are they found? what do they form?

what is function of melanin?

A

derive from neural crest cells, found in Basale, form melanin

melanin protects skin from DNA damage caused by UV radiation

89
Q

what are the two layers of the dermis? what is in each?

define functions of:

  • merkel cells
  • meisner corpuscles
  • ruffini endings
  • pacinian corpuscles

what is in the hypodermis?

A
  • papillary layer - loose connective tissue
  • reticular layer - dense
  • merkel cells - sensory receptors responsible for deep pressure and texture sensation
  • meisner corpuscles - respond to light touch
  • ruffini endings - respond to stretch
  • pacinian corpuscles - respond to deep pressure and vibration

fat and fibrous tissue

90
Q

what happens during sweating?

what happens during shivering/goosebumps?

A

body temp rises, postganglionic sympathetic neurons that use ACh innervate sweat glands which secrete water and ions. vasodilation occurs to maximize heat loss, and heat is absorbed from body by environment when sweat evaporates

body temp decreases, arrestor pili muscles contract causing piloerection (hairs stand up). this traps layer of heated air near skin, vasoconstriction occurs, and skeletal muscles contract rapidly causing ATP to be used but released as thermal energy

91
Q

what portion of nephron is sodium NOT ACTIVELY TRANSPORTED out?

primary function of nephron is to create that is ______ to the blood

A

thin portion of ascending limb of loop of henle

HYPERTONIC

92
Q

difference between red and white fibers

which types of muscles exhibit myogenic activity? explain

what do intercalated discs do? which type of CAM hold them together?

A

red fibers (slow-twitch) fibers have HIGH MYOGLOBIN content and derive energy aerobically, and contain many mitochondria. white fibers (fast-twitch) contain less myoglobin and fatigue quickly

smooth and cardiac muscle; muscle cells respond to nervous input but don’t require external signals to undergo contraction

intercalated discs hold cardiac muscle cells together, and contain many gap junctions

93
Q

how does the # of nuclei per cell vary b/w muscle types?

A

skeletal has many nuclei per cell, smooth has 1 nuclei per cell, cardiac has 1-2

94
Q

what does each letter represent in sarcomere? (mnemonic)?

  • Z
  • M
  • I
  • A

define myofibril, muscle fiber, muscle

A
  • Z - defines boundaries of sarcomere (end of alphabet/end of sarcomere)
  • M - MIDDLE of MYOSIN
  • I - only thin (actin) filaments (I is thin, only thin)
  • A - ALL of thick filament (myosin)

myofibrils are repeating sarcomere units, muscle fiber is many myofibrils, a muscle is many muscle fibers

95
Q

define the following:

  • sarcoplasmic reticulum
  • sarcoplasm
  • sarcolemma
  • T-tubules
  • titin
A
  • sarcoplasmic reticulum - covering that surrounds myofibrils, contains A LOT OF Ca2+
  • sarcoplasm - modified cytoplasm located just outside SR
  • sarcolemma - cell membrane of myocyte
  • T-tubules - perpendicular to myofibrils, they distribute AP’s to all sarcomeres
  • titin - anchors actin/myosin and prevents excessive stretching
96
Q

explain a muscle contraction from contraction to relaxation

Of I, H, Z, A, what changes and what stays the same during muscle contraction?

A

NS sends efferent signal to synaptic button, releases ACh into synapse and binds to sarcolemma, causing DEPOLARIZATION which triggers AP which spreads down sarcolemma and T-tubules to SR. SR releases Ca2+ which bind to TROPONIN, triggering conformational change of TROPOMYOSIN, exposing myosin binding sites on ACTIN. The free globular heads of MYOSIN bind to sites and pull, drawing thin filaments toward M-line, shortening sarcomere, which releases Pi and ADP. Then, ATP binds myosin head again, releasing it from actin and is hydrolyzed

I and H shorten while A and Z stay the same

97
Q

what happens w/ ACh and Ca2+ during relaxation?

what is latent period in muscle contraction?

what is tetanus?

A

ACh is degraded in synapse by AChase, allowing sarcolemma to repolarize, and Ca2+ release ceases and Ca2+ is taken up by SR.

latent period is time b/w reaching threshold and onset of contraction, when AP spreads along muscle allowing Ca2+ to be released

when muscle contractions become so frequent that muscle is unable to relax and becomes fatigued

98
Q

what are two supplemental energy reserves in muscle?

what does the axial skeleton consist of?

what tissue does bone derive from?

A
  1. creatine phosphate can be created during times of rest
  2. myoglobin reserves can be used for muscles during activity

skull, spinal cord, ribcage, hyoid bone

embryonic mesoderm

99
Q

what are trabeculae?

where is marrow produced? red vs. yellow marrow

diaphysis vs. metaphysis vs. epiphysis

tendons vs. ligaments

A

the bony points in spongy bone?

produced in the cavities b/w trabeculae

  • red is filled w/ hematopoietic stem cells (generate cells in blood)
  • yellow composed of fate and is inactive

diaphysis are cylindrical shafts of bones, metaphysis are the wider parts of bones, and epiphysis is the ends of each bone

tendons connect muscle to bone, ligaments hold bones together at joints

100
Q

what are the organic and inorganic components of bone matrix?

describe the following:

  • osteons
  • lamellae
  • haversian vs volkmann’s canals, what do they contain?
  • lacunae
  • canaliculi
A
  • organic - collagen, glycoproteins, other peptides
  • inorganic - Calcium, phosphate, hydroxide
  • osteons (haversian systems) - structural units of matrix
  • lamellae - concentric circles of bony matrix in osteons
  • haversian vs volkmann’s canals - haversian are longitudinal, volkmann’s are transverse; contain vessels, fibers
  • lacunae - small spaces b/w lamellar rings that house osteocytes (mature bone cells)
  • canaliculi - tiny channels that connect lacunae that allow for exchange of nutrients/wastes
101
Q

what are the functions of osteoblasts and osteoclasts?

how does PTH affect bones? vit. D?

how does calcitonin affect bone growth?

A
  • osteoblasts build bone
  • osteoclasts (macrophages) resorb bone

PTH released by parathyroid glands in response to LOW Ca2+, promotes resorption of bone and increases Ca2+ and phosphate in blood
- vit.D is activated by PTH, causes resorption and thus encourages bone growth.

calcitonin is released by parafollicular cells of thyroid in response to HIGH Ca2+, promotes bone formation and lowers Ca2+ levels

102
Q

what is chondrin?

endochondral ossificaiton vs intramembraneous ossification (where does it happen?

T or F the periosteum can differentiate into osteoblasts?

A

chondrin is firm/elastic matrix of cartilage

endochondral is process of cartilage hardening into bone, the cause of formation of long bones. intramembraneous is when undifferentiated embryonic connective tissue is transformed into/replaced by bone
- IN SKULL

TRUE

103
Q

define the following about joints:

  • synovial capsule -
  • synovium -
  • articular cartilage -

origin vs. insertion of bones

flexor vs. extensor
abductor vs adductor
medial vs lateral

A
  • synovial capsule - encloses joint cavity
  • synovium - layer of soft tissue which secretes synovial fluid (lubricates)
  • articular cartilage - coats articular surfaces of bone so impact is restricted to lubricated joint cartilage, not bones

origin is end with larger muscle attachment, insertion is end with smaller attachment

  • flexor vs. extensor - flexor decreases angle, extensor increases angle
  • abductor vs adductor - abductor moves part of body away from midline, adductor moves it closer
  • medial vs lateral rotation - medial rotates axis of limb toward midline, lateral rotates away
104
Q

what is hemizygous?

complete dominance vs. codominance vs. incomplete dominance

penetrance vs. expressivity (constant and variable)

A

when only one allele is present for a given gene (parts of X chromosome for males)

complete dominance is one dominant and one recessive, codominance is when both are dominant (AB blood type), and incomplete dominance is when heterozygote expresses phenotype b/w both (pink flower)

penetrance is proportion of pop. w/ given genotype who actually express the phenotype; expressivity is diff. manifestations of same genotype across pop.
- constant expressivity is when all individuals w/ genotype express same phenotype, variable is same genotype but diff. phenotype

105
Q

segregation and independent assortment allow for greater _________ in offspring

the centromere is where the ________ and ________ are held together

what is recombination in chromosomes?

A

genetic diversity

daughter strand and parent strand

small segments of genetic material are swapped b/w chromatids in homologous chromosomes

106
Q

what is transforming principle?

mutation vs. wild type?

what is a transposon?

A

live, nonvirulent bacteria must have acquired the ability to form smooth capsules from dead virulent bacteria

mutation is change in DNA sequence of allele, while WT is normal/natural allele

an element that can insert/remove itself from DNA, causing mutation if in coding region

107
Q

define the diff. point mutations (1 nucleotide swapped for another)

  • silent
  • missense
  • nonsense

what is a frameshift mutation?

what does it mean if a mutation is deleterious? what are inborn errors of metabolism?

A
  • silent - when change in nucleotide has no effect on final protein synthesized because of degeneracy
  • missense - change in nucleotide result sin substituting 1 AA for another
  • nonsense - when change in nucleotide results in substitution of STOP codon for AA

frameshift is when codon is inserted/deleted into genome

the mutation is detrimental to the organism
- inborn errors of metabolism are a type of deleterious mutation where there are defects in genes required for metabolism

108
Q

what is genetic leakage?

define the following:

  • genetic drift
  • founder effect
  • bottlenecks

what is inbreeding depression? outbreeding/outcrossing?

A

leakage is a flow of genes b/w species, sometimes producing hybrid offspring

  • genetic drift - changes in composition of gene pool due to chance (more pronounced in small populations)
  • founder effect - extreme case of genetic drift, small pop. finds itself in reproductive isolation from other populations as a result of natural barriers (or other bottlenecks)
  • bottlenecks - drastically/suddenly reduce size of pop. available for breeding

inbreeding depression is the loss of genetic variation and a reduce in fitness of pop. outbreeding is introduction of unrelated individuals to group to increase variation

109
Q

what is a test cross?

sex linked traits apply to X or Y?

what is the relationship b/w recomb. freq. and distance b/w genes

what is chiasma?

A

organism w/ unknown genotype is crossed w/ known homozygous recessive

  • if all offspring are dominant, other is homozygous dominant
  • if 1:1, heterozygous
  • if all recessive, other is recessive too

X

they are proportional

point where 2 genes cross over

110
Q

if 2 genes are 29 map units apart, what does that say about recombination?

what are 5 criteria for HW equilibrium?

A

29% of total gametes examined would show recombination somewhere b/w these two genes

  1. pop is very large (no drift)
  2. no mutations
  3. mating is random (no sexual selection)
  4. no migration in or out
  5. genes are all equally successful
111
Q

T or F individuals evolve

what is inclusive fitness?

what does punctuated equilibrium suggest?

A

FALSE populations evolve

measure of organism’s succession pop. based on # offspring, success in supporting offspring, etc.

changes in some species occur in rapid bursts rather than evenly over time (opposes darwin)

112
Q

stabilizing vs. directional vs. disruptive selection

what are polymorphisms?

A
  • stabilizing keeps phenotypes within a specificities range by selecting against extremes (e.g. human birth weight)
  • directional is when adaptive pressure leads to dominance of initially extreme phenotype (e.g. bacteria that are resistant to antibiotics)
  • disruptive is when 2 extreme phenotypes are selected over the norm (e.g. finch beak size)

naturally occurring differences in form b/w members of same pop. (e.g. light&dark coloration of same butterfly)

113
Q

what is adaptive radiation in the context of species? what is its benefit?

what is a niche?

A

describes rapid rise of a # of diff. species from a common ancestor
- benefit is that it allows for various species to occupy diff. niches

niche is specific environment (habitat, available resources, predators) for which a species is specifically adapted

114
Q

prezygotic vs. postzygotic mechanisms

what happens if isolation occurs?

A

prezygotic prevent formation of zygote completely (e.g. breeding at diff times, diff niches, lack of attraction), postzygotic allow for gamete fusion BUT yield nonviable OR sterile offspring (offspring that can’t reproduce, infertile second generation)

the progeny of these populations could no longer freely interbreed. (separate species now)

115
Q

divergent vs. parallel. vs convergent evolution

what is the molecular clock model?

A
  • divergent is independent dev. of dissimilar characteristics in 2 or more lineages sharing a common ancestor (e.g. seals and cats are both mammals, yet differ in general appearance)
  • parallel is process that related species evolve in similar ways for a long period of time in response to analogous environmental pressures
  • convergent is independent dev. of similar characteristics in 2 or more lineages not sharing a common ancestor (e.g. fish and dolphins)

more similar genomes b/w two species, more recent they separated from one another