final DNA replication problems Flashcards

1
Q

what do adaptor proteins do

A

help hold other proteins together

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2
Q

what are gene regulatory proteins

A

transcription factors that play a key role in defining the level of transcription

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3
Q

what are clathrin coat proteins important for

A

forming vesicles as they bud off from membrane - identify the origin membranes of the vesicle so it can be targeted properly

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4
Q

what are the 3 main error-correcting mechanisms to achieve high fidelity of DNA replication

A

5’-3’ polymerization, 3’-5’ exonucleolytic proofreading, strand-directed mismatch repair

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5
Q

what prevents extension by the polymerase

A

lack of base-pairing by a mismatched nucleotide

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6
Q

why can DNA polymerase only extend a base-paired primer

A

there is a dependence of perfect base-pairing of -1 base (last nucleotide in chain)

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7
Q

why does DNA replication need a RNA primer

A

it provides a 3’ paired nucleotide bc DNA polymerases can only add onto existing strands of DNA

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8
Q

what does a RNA primer provide

A

a 3’ paired nucleotide for the polymerase to recognize in order to start a chain

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9
Q

what happens to DNA without perfect base pairing

A

DNA will not add another nucleotide

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10
Q

what happens to exonuclease when mismatch occurs

A

exonuclease removes any nucleotides until there is a clean basepair at the 3’ end, then DNA polymerase can add a new nucleotide

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11
Q

what is a newly synthesized, mismatched pair recognized by

A

the presence of an unsealed nick

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12
Q

how can you distinguish between a newly synthesized strand and the original strand

A

the original is unbroken because it has Okazaki fragments sealed with DNA ligase and the newly synthesized is broken

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13
Q

how is a mis-incorporated nucleotide fixed (aka mutation)

A

second cut in new strand is made, then the stretch of DNA is removed, then gap is filled by DNA polymerase and sealed with DNA ligase

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14
Q

what are the three ways that somatic DNA can be damaged

A
  • oxidation of nucleotides
  • hydrolysis cleavage of base away from sugar/groups away from base
  • methylation of nucleotides that can typically happen bc of chemicals to damage DNA
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15
Q

what are the common forms of DNA damage and how are they generated

A

depurination and deamination, by hydrolysis reactions

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16
Q

what is depurination

A

removal of base from sugar - removes purines (G, A)

17
Q

what is deamination

A

removal of amine groups from base to change identity of base

18
Q

how does DNA glycosylation recognize individual damaged bases and remove them

A

base flipping - can be flipped out from double helix because they don’t pair properly

19
Q

what is base excision repair

A

fixes excised bases - results in the surgical removal of the damaged base followed by DNA synthesis and ligation

20
Q

what is a translesion polymerase

A

can replicate damaged DNA

21
Q

why do translesion polymerase added nucleotides not follow Watson-Crick base pairing

A

allows it to jump over a few nucleotides and save the rest of the genome

22
Q

what are the two ways double-stranded breaks can be repaired

A

non-homologous end joining and homologous recombination

23
Q

what does non-homologous end joining do

A

seals ends back together

ends of DNA will be trimmed back to be blunt ends and will be ligated together with DNA ligase

24
Q

what does homologous recombination do

A

chews it back to get gap; ends of broken chromosome will invade and make pairing with sister chromatid. will use sequence of it as template for reconstructing sequence that has been lost, then can be resealed back up together