6.4 DNA Repair Flashcards

1
Q

How do abnormal alleles lead to cell cycle advancement?

A
  • encode proteins that are more active than normal proteins
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2
Q

What genes participate in DNA repair processes?

A
  • Tumor suppressor genes, like p53 or Rb (retinoblastoma)
  • encode proteins that inhibit the cell cycle or participate in DNA repair processes
  • Just one copy of the normal protein can function to inhibit tumor formation
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3
Q

What happens when complementary strands have incorrectly paired bases?

A
  • the hydrogen bonds between the strands can be unstable, and this lack of stability is detected as the DNA passes through this part of the polymerase.
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4
Q

how does the enzyme discriminate which is the template strand, and which is the incorrectly paired daughter strand?

A
  • It looks at the level of methylation: the template
    strand has existed in the cell for a longer period of time, and therefore is more heavily methylated. Methylation also plays a role in the transcriptional activity of DNA
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5
Q

Why is the likelihood of mutations in the lagging strand considerably higher than the leading strand?

A

DNA ligase, which closes the gaps between Okazaki fragments, lacks proofreading ability

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6
Q

What do enzymes encoded by MSH2 and MLH1 do?

A
  • Do mismatch repair by detecting and removing errors introduced in replication that were missed during the S
    phase of the cell cycle
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7
Q

How do the repair mechanisms work?

A
  • Most involve proteins that recognize damage or a lesion, remove the damage, and then use the complementary strand as a template to fill in the gap
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8
Q

What is Nucleotide Excision Repair mechanism and how is it triggered?

A
  • UV light -> Thymine dimers (interfere with DNA rep., gene expression & distorts shape) -> distorts helix & messes up replication -> triggers NER mech.
  • NER mech:
    1. Recog. damage (it’s a bulge)
    2. excision endonuclease (exinuclease) removes oligonulceotide
    3. DNA poly. synth 5’ to 3’ & ligase seals
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9
Q

Base Excision Repair mechanism

A

Thermal energy -> cytosine to uracil -> glycosylase enzyme (rec. & remove) *leaves a -> AP site -> AP endonucl. removes damage -> DNA poly. rep. -> DNA ligase seals

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