Lecture 7: Replication Flashcards

1
Q

deoxyribonucleotide triphosphate (dNTP)

A
  • nucleotide
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2
Q

How do prokaryotes replicate their DNA?

A
  • DNA polymerase unzips helix
  • 5’–>3’ in both directions
  • replication forks and bubbles (see notes)
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3
Q

synthesis of leading strand (2 steps) (4 key enzymes/proteins involved in first step, SHPT; 1 involved in second)

A
  1. DNA is opened and primed:
    - primase makes RNA primer (~10 nucleotides long)
    - topoisomerase removes twists
    - helicase opens double helix
    - single strand DNA binding proteins keeps strands separated
  2. DNA polymerase III makes leading strand 5’–>3’
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4
Q

synthesis of lagging strand (5 steps)

A
  1. RNA primer is added
  2. first fragment synthesized
  3. next fragment is synthesized (okazaki fragments)
  4. replace primer (DNA primer I replaces RNA with DNA and goes 5’–>3’)
  5. gap is closed by DNA ligase
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5
Q

How does DNA replication occur in Eukaryotes? What is the problem that eukaryote cells run into at the end of replication?

A
  • similar to prokaryotes except larger and more linear chromosomes with multiple replication forks
  • at the end of replication a problem occurs where there are missing nucleotides at the 5’ end because chromosomes shorten during replication
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6
Q

telomer and telomerase

A
  • telomer: portion of strand (end piece) missing DNA (the unreplicated 5’ end)
  • telomerase binds to a 3’ end and adds nucleotides to lengthen telomer several times; has its own RNA template
  • extended DNA acts as a template for DNA polymerase III
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7
Q

DNA repair:

  • during replication
  • immediately after replication
  • anytime
A
  • during: DNA polymerase proofreads DNA; wrong nucleotides are excised and replaced
  • immediately after replication: mismatched repair occurs on new strand
  • anytime: repair of damaged DNA
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8
Q

enzymes involved in DNA repair (3): state role

A
  • nucleases: excision
  • DNA polymerase: replacement
  • ligase: linkage
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9
Q

genotype vs phenotype

A

genotype: sequence code for protein
phenotype: physical trait produced by protein

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10
Q

List the types of mutations (4)

A
  • silent
  • missense
  • nonsense
  • frameshift
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11
Q

explain the following mutation type and the result of it: silent

A
  • change in nucleotide sequence that does not impact the amino acid specified by codon
  • result: no change in phenotype
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12
Q

explain the following mutation type and the result of it: missense

A
  • change in nucleotide sequence that changes amino acid specified by codon
  • result: change in primary structure of protein (could be beneficial, neutral, or deleterious)
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13
Q

explain the following mutation type and the result of it: nonsense

A
  • change in nucleotide sequence that results in an early stop codon
  • result: breakdown of mRNA or a shortened polypeptide; usually deleterious
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14
Q

explain the following mutation type and the result of it: frameshift

A
  • addition/ deletion of a nucleotide

- result: reading frame is shifted altering meaning of all subsequent codons; almost always deleterious

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15
Q

differentiate between DNA I and DNA III

A
  • dna polymerase I: removes RNA primer with DNA

- dna polymerase iii: adds nucleotides to make new strand

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