Exam 2 Flashcards

1
Q

What is transcription

A

DNA -> mRNA

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2
Q

Central Dogma

A

DNA -> RNA -> Protein

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3
Q

Enzyme for RNA

A

Ribozyme

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4
Q

RNA vs DNA (just RNA)

A

RNA:
- Uracil instead of Thymine
- Ribose instead of deoxyribose
- Can fold into different structures

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5
Q

What catalyzes RNA trasnscription?

A

RNA Polymerase

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5
Q

Functions of RNA polymerase

A

Catalyzes RNA transcription
Unwinds the strands
Keeps strands seperate

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5
Q

Coding vs non coding strand

A

Coding: The one that will look like your new strand but you don’t touch
Noncoding: The one you touch but is the opposite of your new strand

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6
Q

What is translation

A

mRNA -> polypeptide

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7
Q

Steps of eukaryotic transcription and where they’re located

A
  1. Transcription: in nuclear envelope
    DNA -> Pre-mRNA
  2. RNA processing
    Pre-mRNA -> mRNA
  3. Translation: Leaves nuclear envelope
    mRNA -> Polypeptide
    Done by a ribosome
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8
Q

Prokaryotic transcripts are often

A

polycistronic (multiple proteins encoded on one mRNA)

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9
Q

Eukaryotic vs Prokaryotic mRNA

A

Eukaryotic:
- mRNA processing (pre -> mRNA)
- leaves nuclear envelope for translation
- One mRNA for one protein

Prokaryotic:
- No processing (no splicing, 5 prime caps, etc.)
- Polycistronic

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10
Q

Three ways pre-mRNA is processed

A
  1. 5’ cap
  2. Splicing (introns are removed)
  3. Poly-A tail
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11
Q

Why do we have pre-mRNA processing?

A
  1. Protects ends
  2. Marks ready for translation
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12
Q

What does the 5’ cap bond to?

A

triphosphate group bridge

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13
Q

What splices the pre-mRNA

A

Spliceosome

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14
Q

What is a spliceosome made of and how does it work

A

Made of snRNPs and other proteins. It hydrogen bonds with the introns to form and intron loop

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15
Q

What is alternative splicing and what is the outcome?

A

Recombines exons to form different patterns. It can distinguish protein functions out of one gene.

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16
Q

What distinguishes pre-mRNA to mRNA and allows mRNA to leave the nucleus?

A

Nuclear Pore Complex

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17
Q

What adds the poly-A tail to mRNA

A

Poly-A polymerase

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18
Q

What interacts with mRNA to translate it?

A

A ribosome

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19
Q

What is a ribosome made of? (overall)

A

rRNA and ribosomal proteins

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20
Q

UTR

A

Noncoding regions binding sites where proteins bind to stop translation

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21
Q

5’ UTR

A

Blocks translation (proteins bind to it)

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22
Q

3’ UTR

A

Bind to microribosomes at post transcription regulation

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23
Q

What subunits make up the ribosome

A

Small subunit and bigsubunit

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24
Q

Why are ribosomes so big

A

They need to bind to 3 tRNA, mRNA, polypeptides, etc.

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25
Q

Polypeptides are made from the

A

N-terminus to the C-terminus

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26
Q

Three factors used in translation

A

Initiation, elongation, and release factors

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27
Q

What brings specific tRNAs to the ribosome

A

Aminoacyl tRNA synthetases

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28
Q

Draw a polypeptide chain being made from n to c terminus

A

okay

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29
Q

Label all the amino acids accordingly

A

Okay

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30
Q

Why is there a triplet code?

A

There are 20 amino acids
1: 4
2: 4 x 4 = 16
3: 4 x 4 x 4 = 64

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31
Q

What does the redundancy of 64 codes when you only need 20

A

diversity of the last codon, allows to be wobbled by tRNA

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32
Q

Initiation

A

Starts at 5’ cap, first AUG is the start codon, and is read 3 at a time

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33
Q

What differentiates amino acids?

A

R groups

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34
Q

Who reads the triplet code in mRNA

A

tRNA

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35
Q

At the ___’ end of tRNA is where amino acids attatch

A

3’ end via an ester bond

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36
Q

How are amino acids grouped with triplet codes

A

The anticodon region reads the mRNA sequence, and an amino acids fits into the attachment site on the 3’ end of the tRNA

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37
Q

What ends the process of translation?

A

hydrolysis

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38
Q

Chromatin

A

DNA + protein fiber that organizes and packages genetic material

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39
Q

Histone

A

Made of 8 proteins, a spool where the DNA is wrapped around

40
Q

How may wraps per histone

A

around 1.5

41
Q

T/F Chromosomes are always condensed

A

F, condensed only during replication

42
Q

Homologous

A

Similar but not identical

43
Q

Diploid

A

Two of each chromosome

44
Q

Humans have __ sets of chromosomes so ____ in total

A

23 sets, 46

45
Q

Why is telomerase only active in germ and stem cells

A

Somatic cells like skin cells should not keep rapidly rejuvenating or else cancer will occur.

46
Q

Sexual reproduction summarized

A

Meiosis:
germ-like cells: haploid egg and sperm fertilize to make a diploid zygote
Mitosis: zygote multiples so form an organism full of somatic and germ cells.

47
Q

Two parts of a chromosome

A

Centromeres and telomeres

48
Q

Direction RNA polymerase reads and synthesizes in

A

Reads: 3’ to 5’
Synthesizes: 5’ to 3’

49
Q

TATA box

A

where RNA polymerase binds to before transcription

50
Q

Direction the ribosome reads and synthesizes during translation

A

Reads: 5’ to 3’
Synthesizes: n terminus to c terminus

51
Q

Describe the EPA

A

E: n-terminus, tRNA ejected
P: connecting polypeptides
A: C-terminus, tRNA enters

52
Q

What happens during s phase

A

2 Homologous chromosomes (1 chromatid each) replicated and make 2 homologous chromosomes (2 sister chromatids each)

53
Q

Which strand needs telomerase to add telomeres to prevent important sequences from being lost?

A

lagging strand

54
Q

What attaches to centromeres to separate sister chromatids?

A

kinetochores attached to long microtubules

55
Q

Three things that allow for genetic diversity

A
  1. Random fertilization
  2. Independent assortment of maternal and paternal homologs during meiosis I
  3. Crossing over during meiotic prophase I
56
Q

Classify as haploid, diploid, and by mass during the stages of cell division

A

Interphase:
2n, 2x
2n, 4x

Meiosis I:
n, 2x

Meiosis II
n, x

57
Q

Steps of Meiosis I

A

Interphase, Prophase I, Metaphase I, telophase I, cytokinesis

58
Q

Interphase

A

Interphase: Chromosomes replicate to make sister chromatids in the parent cell

59
Q

Prophase I

A

Early Prophase I: Chromosomes condense, nuclear envelope breaks up, spindle apparatus forms, Synapsis of homologous chromosomes (form tetrads)

Late Prophase I: Crossing over of nonsister chromatids

60
Q

How do holiday junctions work

A

When it is formed, there is a 50% 50% chance that resolvase slices it to recombine from non sister chromatids. if the out strands are cut, it happens

61
Q

Chiasma

A

the located where non-sister chromatids link in recombination

62
Q

Metaphase I

A

Tetrads migrate to metaphase plate

63
Q

At least one holiday junction needs to form for each chromosome before metaphase I, how can the cell tell?

A

If there is tension when the chromosomes are being pulled apart

64
Q

Anaphase I

A

Homologs separate and begin moving to opposite sides of the cell

65
Q

Telophase I

A

Cells divide

66
Q

What happens during meiosis II?

A

Same as meiosis I but there is no interphase, and four cells are formed. Each with their own nuclear envelope, two chromosomes (each with one chromatid)

67
Q

What solutions did valence bond theory give

A
  1. Considers quantum mechanics
  2. Separate orbitals can’t form proper geometry, so they hybridize
68
Q

What does hybridization do

A

Takes different orbitals and makes them the same size and shape

69
Q

What are sigma bonds

A

Covalent bonds between 2 atoms formed when orbitals overlap

70
Q

What are pi bonds

A

Bonds made when p orbitals overlaps above and below the internuclear axis

71
Q

Why is SP3 lower in the energy diagram than P?

A

It has more s character

72
Q

Paramagnetic

A

Molecules with unpaid electrons, attracted to magnetic fields

73
Q

Diamagnetic

A

Molecules with paired electrons, not attracted to magnetic fields

74
Q

When orbitals (wave functions) are inphase

A

It is constructive and forms a bond

75
Q

When orbitals (wave functions) are outphase

A

It is destructive and forms a node (aka antibond)

76
Q

Valence bond theory vs MO

A

Valence Bond:
- Each atom’s own orbitals hybridize independently

MO:
- All atomic orbitals combine in one molecule

77
Q

Molecular Orbital Theory, 4 principles

A
  1. S and S combine to for a bonding and antibonding MO (sigma and sigma star)
  2. Bonding MOs are lower in energer
  3. Lowest MOs fill first
  4. The number of AOs equals the number of MOs
78
Q

Bond Order (equation and use)

A

Determines strength and length
1/2[(number of electrons in bonding MOs) - (number of electrons in antibonding MOs)]

79
Q

Why does sp mixing happen?

A

2s and 2p are closer in energy when the Zeff is lower

80
Q

Diatomics that will experience sp mixing and wont

A

Yes: Li2, Be2, B2, C2, N2 (anything isoelectric with N2)
No: O2, F2, Ne2

81
Q

The more Zeff

A

The less energy of MO orbitals

82
Q

Intermolecular vs Intramolecular

A

Intermolecular:
- Between two or more molecules
- Dipole-dipole interactions and London dispersion forces
- Hold molecules together (determine melting point, boiling point, etc)
- Weak interactions

Intramolecular:
- Inside a molecule
- Covalent
- Hold atoms together to make a molecule
- Very strong

83
Q

London Dispersion Forces (Vanderwall)

A
  • Instantaneous
  • Temporary dipoles because electrons are always moving
  • Every molecule has it
  • The more there are the higher boiling and melting point
84
Q

Higher surface area =

A

More chance of LDF

  • They can stack better
85
Q

Dipole Dipole

A

Permanent interaction
Electronegative atom

86
Q

Hydrogren Bond

A

The strongest dipole-dipole interaction (due to the difference in EN)

87
Q

Steps to make sure it is hydrogen bond

A
  1. Net dipole
  2. Hydrogen bonded to EN atom
  3. O, N, Br, F
88
Q

Ion-Dipole

A

Interactions like salt and water

89
Q

Percent Yield

A

Actual yield/Theoretical Yield x 100 = % yield

90
Q

Molarity

A

Moles of solute/Liters of solution

91
Q

T/F RNA molecules can synthesize sequentially before the first finishes

92
Q

T/F All genes are transcribed at the same efficiency

A

F, UTR tunes efficiency

93
Q

Transcribe the RNA from this
5’-AGTCTA-3’
3’-TCAGAT-5’

A

5’-AGUCUA-3’

94
Q

Where is hybridization inaccurate?

A

The theory is inaccurate because it assumes that electrons are localized in bonds between atoms or in lone pairs, “belonging” to one atom. In reality, electrons are delocalized across the entire molecule. As a result of this physical inaccuracy, this theory cannot predict the energies of electrons within molecules.

95
Q

Best way different cells maintain different functions

A

Cell specific mRNA transcription

96
Q

Which amino acid would tRNA with the anticodon 5’-CUU-3’ carry?

97
Q

Alpha Helix

A

Coils like a spring, turns every 3.6 amino acids

C=O groups point down to the C-terminus (positively charged)

N-H groups point up to the N-terminus (negatively charged)

98
Q

Beta sheet

A

Two poly peptides stacked on top of one another

Parallel: Same direction
Antiparallel: Opposite directions

99
Q

Nonpolar amino acids tend to be found in the

A

interior of proteins