DNA replication and protein synthesis Flashcards

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1
Q

What did T.H. Morgan group find by studying fruit flies?

A

That genes are located on chromosomes

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2
Q

What became the two candidates for the genetic material ?

A

DNA

Protein

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3
Q

What did Frederick Griffin discover in 1928?

A

He discovered the genetic role of DNA and observed the principle of transformation

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4
Q

What did Avery, McCarty and McLeod find?

A

That transformation only occurred when DNA remained active (so proteins and RNA were not the transforming agent)

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5
Q

What did Hershey and Chase show in 1952?

A

That DNA is the genetic material of a phage called T2

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6
Q

What did Chargaff report in 1950?

A

That in any species, A =T and C = G

That the ration of A+T vs C+G varies among species

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7
Q

Why is DNA replicated?

A

For growth

For reproduction

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8
Q

What is the error rate of DNA replication?

A

1 error per 10 billion nucleotides

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9
Q

What type of replication does DNA undergo?

A

Semiconservative replication

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10
Q

What is the role of helicase?

A

It untwists the double helix at the replication fork.

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11
Q

What is the role of the single-strand binding protein (SSBP) ?

A

It bind to and stabilizes single stranded DNA until it is used as a template

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12
Q

What is the role of topoisomerase?

A

it corrects overwinding ahead of the replication fork by breaking, swiveling anfd rejoining DNA strands

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13
Q

What is the difference between Type I and Type II topoisomerase?

A

Type I cuts only one DNA strand, whereas Type II cuts both strands.

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14
Q

What is the role of primase?

A

It reads the parental DNA (3’ to 5’)

It synthesizes the primer (5’ to 3’)

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15
Q

What is the role of DNA polymerase?

A

It adds nucleotides to the 3’ end of the primer/ growing strand
It catalyses the elongation of new DNA

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16
Q

What is the leading strand?

A

The strand that DNA polymerase synthesizes continuously

DNA polymerase moves towards the replication fork

17
Q

What is the lagging strand?

A

The strand in which DNA polymerase works in the direction away from the replication fork