Lecture 11 Flashcards

1
Q

What are the characteristics of a large DNA molecule replicated

A

Multiple large linear chromosomes (23 pairs in humans)
Multiple origins (starting points) of replication
bidirectional

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2
Q

Where do replication bubbles begin

A

a=t double hydrogen bond region as it is easier to pull the strand apart

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3
Q

What is needed in a DNA copy

A

addition of new nucleotides
a starting point for nucleotide
the unwinding of the helical double-stranded DNA.

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4
Q

What happens to the leading strand in DNA replication

A

Continuously synthesised in the 5-3 direction

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5
Q

What happens to the lagging strand in DNA replication

A

Discontinuously synthesised 5-3 as Okazaki fragments

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6
Q

What is Primase

A

the enzyme that makes RNA primer—–starting point for DNA Polymerisation

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7
Q

How does DNA polymerase III function

A

Needs an OH group onto which the phosphate group of the incoming nucleotide can be attached
only makes DNA in 5’ to 3’ direction

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8
Q

How does DNA polymerase III synthesise DNA

A

it synthesises a new DNA strand by adding complementary nucleotides to the parental template strand
Cannot bind to single-stranded DNA and start copying it

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9
Q

How does DNA replication initiate

A

Helicase pulls the DNA strands apart
single strand binding proteins (SSBP)- protect from enzymes and keep strand apart
Topoisomerase- cuts DNA to release tension, then rejoins it

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10
Q

What does primase make

A

Makes short RNA 5-3 with OH group to react with other strands

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11
Q

What does DNA polymerase III do to SSBP

A

after DNA polymerase III adds nucleotide it removes SSBP then synthesis of the leading strand continues

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12
Q

How is the lagging strand synthesized

A

RNA primers from primase go 5-3, DNA polymerase III uses RNA primers to add nucelotides 5-3

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13
Q

What is the role of Polymerase I

A

it recognizes the DNA, RNA hybrid strand and replaces it with nucleotides from Okazaki fragments that are not linked

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14
Q

What is the role of Ligase

A

it uses 3’ OH and 5’P to create a phosphodiester bond

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15
Q

how are Errors in the DNA removed

A

during-exonuclease removes errors from the 3’ or 5’ ends

after-endonuclease, chops nucleotides from the middle of the strand

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16
Q

What proofreads the DNA for errors

A

DNA polymerase checks newly inserted base against the template

17
Q

What causes DNA damage after

A

error bases not corrected, radiation damage, chemical modification
endonuclease removes errors

18
Q

What happens if DNA errors are not corrected

A

permanent DNA change, damage or mutation

19
Q

What is Polymerase Chain Reaction (PCR)

A

a fast method of quickly making DNA material to work with targets regions and the exponential increase of DNA molecules

20
Q

What is the Process of PCR

A

Denaturation-temp increases to seperate DNA strand
Annealing- temp is decreased to allow primers to base pair
Extension-Polymerase extends primer for nascent DNA strand
up to 35 times
2^number of times