D1.1 Replication Flashcards

1
Q

When is DNA replication carried out in eukaryotic cells?

A

Before mitosis and meiosis

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2
Q

What is DNA replication before mitosis required for?

A

Growth and tissue replacement

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3
Q

What is DNA replication before meiosis required for?

A

Reproduction

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4
Q

What allows for the high degree of accuracy in DNA replication?

A

Complementary base pairing

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5
Q

Meselson and Stahl Experiment

A
  • Proved that DNA replication is semi-conservative
  • Grew many generations of E.coli cells in a medium containing only heavy nitrogen (15N). Created a low band when centrifuged.
  • DNA was then introduced to a medium with only light nitrogen (14N).
  • After one generation the band was higher.
  • After the 2nd gen, there was 2 bands one for hybrid DNA and one for the DNA with only light nitrogen
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6
Q

Steps of DNA replication

CHECK!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

A
  • Coiled DNA is allowed to uncoil
  • The double helix is unwound by DNA gyrase
  • Helicase “unzips” the rungs of DNA by breaking the weak hydrogen bonds
  • New pieces of DNA are formed from free nucleotide units by DNA polymerase
  • The free nucleotides are matched up by complementary base pairing
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7
Q

What is the advantage of complimentary base pairing in DNA replication?

A

It allows almost perfect/identical copies to be made, ensuring mutations are avoided as often as possible.

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8
Q

DNA replication is semi-conservative, what does this mean?

A

Semi-conservative essentially means 1/2 original. This means that the original strand is split in half and a new half to each strand is formed via complementary base pairing. This leaves you with two new strands each containing half the original strand of DNA.

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9
Q

What is DNA amplicfication?

A

Tiny pieces of DNA being copied many times to form billions f copies of that DNA. Can be done with the Polymerisation chain reaction (PCR)

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10
Q

What is required for PCR?

A
  • The DNA to be amplified
  • Buffer solution
  • Primers
  • Taq DNA polymerase
  • DNA nucleotides (ATCG)
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11
Q

What is the role of Buffer solution in the PCR?

A

It allows the necessary reactions to occur by keeping the pH suitable for the enzymes.

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12
Q

What is the role of primers in the PCR?

A

Primers are the complimentary sequence to the DNA you want replicated.

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13
Q

What is the role of Taq DNA polymerase in the PCR?

A

It attaches to the primer and creates a new strand of DNA nucleotides by complimentary base pairing. It can tolerate the high temps used to speed up the rate of rxn.

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14
Q

Steps in the polymerisation chain reaction (PCR)

A
  • Denaturing (strands split in 1/2)
  • Annealing (Primers attatch
  • Extension (A new strand is synthesised)
  • DNA is cut into fragments by restriction enzymes before analysis
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15
Q

What is Gel electrophoresis used for?

A

To seperate proteins or DNA fragments by size.

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16
Q

Steps of Gel electrophoresis

A
  • An agarose gel with wells in it is placed in a chamber that allows electricity to be pass through the gel
  • The prepared DNA is injected into the wells
  • The electrodes are turned on, causing the DNA to move towards the positive electrode (DNA IS strongly neg)
  • The size of the DNA can be calculated by the rate of travel
17
Q

Common applications for PCR and gel electrophoresis

A

Forensic analysis and paternity testing.