week 5 (unit 2) Flashcards

1
Q

RNA

A
  • single-stranded (most)
  • bases: UTCG and ribose sugar
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1
Q

DNA

A
  • double-stranded, genetic material
  • bases: ATCG and deoxyribose sugar
  • semiconservative
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2
Q

eukaryotic DNA characteristics
(fungi and protists)

A
  • linear, in nucleus, telomeres, introns, multiple chromosomes, and strands twist
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3
Q

prokaryotic DNA characteristics
(bacteria and archaea)

A
  • circular, in cytoplasm, one chromosome, one origin of replication -> bidirectional replication
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4
Q

levels of protein structure

A
  • primary: amino acid sequence
  • secondary: alpha helix or beta sheets
  • tertiary: 3D structure (polypeptide structure)
  • quaternary: 2 or more polypeptide structures
    —– hemoglobin
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5
Q

7 enzymes involved in DNA synthesis

A
  1. helicase: breaks the H bonds
  2. ssDNA binding proteins: protects the DNA and keeps the strands apart
  3. topoisomerases: relieves twisting and keeps it loose
  4. primase: synthesizes the short RNA primers on the lagging strand for the DNA polymerase
  5. clamp loader complex: holds teh DNAP at the DNA strand
  6. Tau: binds E. Coli replication proteins
  7. DNA ligase: joins the Okazaki fragments
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6
Q

leading strand

A
  • primase and DNAP replicate easily in the 5’ to 3’ direction (MEANING THE DNA STRAND THAT IS 3’ FROM THE LEFT SIDE)
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7
Q

lagging strand

A
  • primase and DNAP replicate in many fragments and DNA ligase joins them when done
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8
Q

what enzyme has exonuclease activity (proofreading) , remove wrong nucleotide and out the correct one in

A

DNAP

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9
Q

what does central dogma refer to?

A

DNA-> RNA -> protein

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10
Q

is it in prok. or euk. that transcription and translation occur at the same time (coupled)?

A

prokaryotes

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11
Q

difference between DNAP 1 and DNAP 3?

A
  • DNAP 1 is used to synthesize the DNA from the RNA primers
  • DNAP 3 does the proofreading
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12
Q

bacterial RNAP

A

pic

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13
Q

for transcriptional initiation, whats the composition of the promoter fro both prok and euk?

A
  • euk: TATA box
  • prok: pribnow box
    —- both are heavy TATA heavy regions
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14
Q

promoter region

A
  • -35 bps upstream: sigma factor recognizes and binds
  • -10: Pribnow box: strands start to separate
  • +1: transcription starts
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15
Q

what proteins block the RNAP from binding?

A

repressor proteins on the operator region

16
Q

what proteins help the binding of RNAP?

A

activator proteins on the enhancer region

17
Q

bacterial transcriptional elongation

A

the mRNA strand continues to grow

18
Q

bacterial transcriptional termination: 2 ways

A
  • intrinsic (stem loop): RNA sequence makes a hairpin which is weak bc of AU base pairs and then strand is released
    —— 1. hairpin structure: pause
    2. poly U sequence: ends
  • factor dependent Rho protein (helicase): Rho binds to the rut site and moves along the strand and until it catches up to the termination site and then teh strand is released
19
Q

bacterial translational initiation

A
  • rRNA is w/ mRNA and tRNA binds to the Shine Dalgarno sequence (start codon) on the mRNA
    —–initiator tRNA = N-formylmethionine
    —–archaea and euk: initiator tRNA= methionine
20
Q

euk translational initiation

A

the tRNA binds to the 5’ cap and 3’ polyadenine tail instead of the shine dalgarno sequence (euk doesn’t have this)

21
Q

bacterial translational elongation

A

-mRNA strand is moving along teh ribsome and the tRNA is providing teh amino acid
- tRNA is moving form A-> P -> E sites
- 2 rare stop codon: selenocysteine and pyrrolysine

22
Q

bacterial translational termination

A

when the stop codon is reached the ribosome disassembles and the polypeptide chain is released

23
Q

where do the proteins go when they are synthesized?

A

from cytoplasm to across the plasma membrane

24
Q

2 protein movement systems

A

sec: general secretion pathway
tat: specialized for folded proteins

25
Q

protein secretion in gram (-) bacteria