DNA Chemistry and Replication Flashcards

1
Q

What was the question asked in Griffiths Transformation Experiment?

A

Is there a transforming principle?

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2
Q

Explain briefly how Griffiths underwent his experiment

A

Took rough and smooth strains, S was virulent and R was not. He injected them both into mice, the S strain killed the mouse. A heat killed S strain did not kill the mouse, but when mixed with R strain it did. This is because the R strain picked up the ability to cause disease from the environment (it transformed).

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3
Q

What was Avery, MacLeod and McCarty’s experimental question?

A

What is the transforming principle?

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4
Q

Explain Briefly how A, M, M underwent their experiment

A

Used different enzymes for degradation of cellular components (protease, Dnase, Rnase) Injected mice with heat killed S strain and R strain, the one with Dnase lived. Therefore DNA is the transforming principle, not proteins.

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5
Q

What was Hershey and Chases question

A

Is DNA the universal transforming principle?

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6
Q

Briefly explain H and C’s experiment

A

Used virus that infects bacteria (phage) to label proteins and DNA (S35 for proteins, P32 for DNA), found that the viral DNA enters the bacterial cell and the viral proteins do not (DNA’s pellet was radioactive)

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7
Q

What is Chargaffs rule

A

%A=%T

%C=%G

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8
Q

What did James Watson and Francis Crick discover

A
  • DNA is a double helix (used work of others: Chargaff and Rosalind Franklin)
  • A pairs with T, C pairs with G
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9
Q

What are the three forces that stabilize DNA

A
  1. Phosphodiester bonds
  2. H-bonds
  3. Hydrophobic base pairing
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10
Q

When does DNA replication occur

A

S phase

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11
Q

What did Meselson-Stahl attempt to detemine

A

Is DNA replication conservative, semiconservative or dispersive (can you picture the models in your head?)

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12
Q

Briefly Describe Meselson-Stahl’s experiment

A

Used radioactivity to change molecular mass of N (N15= heavy nitrogen). One round of replication in N14 lead to observed intermediate band, conservative rep was disproved. Second round of replication in N14 led to one N14 band and one N14.5 band. Rules out dispersive cause we would have expected N14.25 band.

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13
Q

What direction is DNA polymerized

A

5’ -> 3’ (nucleotides added to 3’ end)

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14
Q

What is deoxyribonucleotide?

A

substrate of replication

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15
Q

What is the enzyme of replication and what does it do

A

DNA polymerase

catalyzes phosphodiester bond formation

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16
Q

What enzyme unwinds the double helix

A

helicase

17
Q

What is the role of DNA polymerase III

A

Adding nucleotides (in the 3’ to 5’ direction)

18
Q

What keeps the bubble unwound?

A

Single stranded binding proteins

19
Q

The ______ strand is synthesized discontinuously in small fragments called _______ __________.

A
  1. lagging strand

2. okazaki fragments

20
Q

What connects the okazaki fragments?

A

DNA ligase

21
Q

What is the role of primase in replication

A

Synthesizes an RNA primer at 5’ end of lead strand and each okazaki fragment.

22
Q

What is the role of polymerase I?

A

Remove RNA nucleotides that primase put at the 5’ end and replaces them with DNA nucleotides