DNA replication in vivo Flashcards

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1
Q

in the cell, what is the primer?

A

RNA

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2
Q

DNA polymerase properties

A

reads template sequence and links nucleotides

reads 3’ to 5’ and synthesizes new DNA 5’ to 3’

MUST always start from on existing 3’ OH end of an existing template

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3
Q

semi conservativeness of dna replication

A

one strand from parent one new

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4
Q

function of helicase

A

breaks hydrogen bonds between base pairs and unwinds the DNA double helix

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5
Q

function of primase

A

synthsizes RNA primers on DNA leading and lagging strands

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6
Q

function of DNA pol. I

A

replaces RNA primers with DNA nucleotides

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7
Q

DNA ligase

A

catalyzes phosphodiester bond formation, joining DNA fragments on lagging strand

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8
Q

function of topoisomerase

A

relaxes supercoiled DNA

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9
Q

SSBPs

A

coat single stranded DNA

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10
Q

DNA Pol. III

A

synthesizes DNA 5’ to 3’ on leading and lagging strands

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11
Q

the leading strand has what ‘ end of the strand pointing to/ at the replication fork

A

the 3’ end, because bases are added from 5’ to 3’ therefore can be added directly as the dna unwinds

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12
Q

how many replication forks are there in one replication bubble

A

2

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13
Q

where is the origin of replication located and how many are there in 1 replication bubble

A

right in the middle of the middle of the bubble, like at the top of a bridge, there is one origin or replication for each bubble which is where replication in both directions begins

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14
Q

replication with circular DNA

A

generally only one origin of replication (generally called OriC)

replicates in a circle, engds generally meet up

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15
Q

replication with linear DNA

A

can begin at any origin of replication , eukaryotes have many many

more than one origin or replication (gen called OriR)

when 2 replication forms meet they fuse to form one large bubble

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16
Q

process of separating the DNA strands

A

topoisomerase relives stress of unwinding, while helicase unwinds, single-strand binding protein (SSB) stabalizes the single strands of DNa

17
Q

process of making primers for DNA replication

A

DNA poly req a primer sequence so it can add to a 3’OH group, RNA primase synthesizes an RNA primer which DNA polymerase can extend

18
Q

what creates the RNA primers

A

the enzyme primase

19
Q

fragments of dna on lagging strand

A

okazaki fragments

20
Q

leading vs lagging strand

A

leading strand has 3’ end facing towards replication fork therefore can continuously grow (located on DNA template strand w/ 5’ end at fork)

lagging strand has 5’ end towards for, therefore must be synthesized in small fragments (okazaki fragments) which are joined by dna ligase which catalyzes formation of phosphodiester bonds to join the fragments. before ligase links the fragments, DNA polymerase 1 must replace the RNA primers with DNA