MB - DNA Replication (Eukaryotes) Flashcards

1
Q

What are the overall similarities between eukaryotic and prokaryotic DNA replication? (4)

A
  1. Use helicases to unwind the duplex and create replication forks
  2. Use SSBs to hold the ssDNA apart
  3. Use RNA primers for the polymerase/clamp
  4. Use various DNA polymerases for the synthesis of the new DNA on leading and lagging strands
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2
Q

What are some broad differences between eukaryotic and prokaryotic DNA replication? (5)

A
  1. Occurs in the nucleus, not the cytoplasm
  2. More genetic material to replicate (can be four orders of magnitude greater)
  3. More than one chromosome (46 in humans)
  4. Linear chromosomes (except mitochondrial)
  5. Additional packaging (e.g. nucleosomes)
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3
Q

What are some specific differences in eukaryotic DNA replication? (5)

A
  1. Multiple origins per chromosome (10s-1000s)
  2. DNA polymerases are much slower
  3. No DNA polymerases with 5’-3’ exonuclease
  4. Polymerases synthesising leading and lagging strands are not physically linked together
  5. Okazaki fragments are much shorter
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4
Q

How often does initiation occur per cell cycle?

A

Must only happen once per cell cycle
- Ensured by a 2-step process

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5
Q

Where do Origins of replication arise from?

A

Sections of DNA called Autonomously Replicating Sequences (ARS)

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6
Q

What happens during initiation/licensing in the G1 phase of the cell cycle? (3)

A

1) An Origin Recognition Complex of proteins (ORC) binds to the A region

2) Accessory proteins (licensing factors) accumulate in the nucleus during G1

  • Cdc6 and Cdt1 bind to ORC

3) Two helicases are loaded by Cdt1

  • Cdc6/Cdt1 leave
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7
Q

What happens during initiation/activation in the S phase of the cell cycle?

A

The pre-replication complex must be activated

  • Activated by additional proteins + DNA polymerases
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8
Q

What polymerases are involved in DNA elongation in eukaryotic replication? (5)

A

Polymerase α
- Has own primase activity
- Does not associate with PCNA (so not progressive)
- No proofreading

Polymerase β
- Involved in repair

Polymerase γ
- Replicates mtDNA
- Has proofreading

Polymerase δ (lagging strand)
- Associates with PCNA (sliding clamp protein)
- Has proofreading

Polymerase ε (leading strand)
- Associates with PCNA
- Has proofreading

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9
Q

What are 2 methods of editing in elongation?

A

RNA “flap” produced by Pol δ or ε can be mostly digested by RNAse H1
- 1 RNA nt left
(like E.coli version)

Flap 1 endonuclease (FEN1) binds PCNA and can remove any incorrect nt
- Cuts off a section of ssDNA/RNA

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10
Q

What is the end replication problem in DNA replication?

A

Affects the lagging strand

  • Last RNA primer may not be at the extreme 3’ end of the DNA→missed section
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11
Q

How is the end replication problem addressed in eukaryotic cells?

A

Telomeres
- Multiple repeats of a simple sequence (TTAGGG) located at the 3’ ends of chromosomes

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12
Q

How do embryonal cells, cancer cells, stem cells and other types divide more times than the Hayflick limit?

A

→ Synthesis of new telomeric DNA

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12
Q

What happens when the telomeric DNA is gone? (2)

A

→Gene loss
→Cells stop dividing, a point called the Hayflick limit

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13
Q

How is DNA replication handled in mitochondrial DNA? (4)

A
  1. 2-10 copies of circular mtDNA per mitochondrion
  2. Unidirectional replication (1 fork)
  3. Pol γ synthesizes leading strand
  4. Lagging strand is RNA Okazaki fragments
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14
Q

What are the replication mechanisms used by bacteriophages, RNA genomes, and retroviruses?

A

Bacteriophages
- Small circular genome
- Some use a “rolling circle” mechanism to continuously synthesize new DNA
- Sigma (σ) replication

RNA genomes
- Have an RNA-dependent RNA polymerase called RNA replicase
- +Strand RNA is copied directly to make - strand (which is used as a template for more + strand)
- Can be self-priming – no primer is required
- No proof-reading → highly error-prone

Retroviruses
- Virally encoded reverse transcriptase creates a DNA strand using RNA as a template and tRNALys as a primer

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