2.7 DNA -> Protein Flashcards

1
Q

Why do we say DNA replication is semi-conservative?

A

One strand is from the original molecule and one is newly synthesised

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2
Q

Which enzymes are involved in the replication of DNA?

A

Helicase

DNA Polymerase

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3
Q

Who confirmed DNA replication was semi conservative and when?

A

Meselson-Stahl in 1958

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4
Q

Describe what a dispersive model of DNA would have meant?

A

New molecules were thought to be made of segments of old and new DNA

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5
Q

Describe what a conservative model of DNA would have meant?

A

An entirely new molecules is synthesised from an (unaltered) DNA template

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6
Q

How did Meselson and Stahl prove that DNA replication was semi-conservative?

A

DNA was prepared in heavy 15 N (nitrogen) and then allowed to replicate once in 14 N
After 1 replication they were found to contain a mix of 14 and 15 N and after 2 replications some showed only 14N or only 15 N

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7
Q

What disproved the conservative model?

A

That after 1 replication in N14, the DNA molecules contained a mix of N14 and N15

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8
Q

What disproved the dispersive model?

A

That after 2 replications in N14, some DNA molecules were only N14

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9
Q

What is the function of helicase?

A

Unwinds the double helix by breaking hydrogen bonds

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10
Q

What is the function of DNA polymerase?

A

Synthesises new strands by aligning complementary base partners

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11
Q

Where does the energy come from for DNA polymerase to add the bases?

A

The nucleotides are in triphosphate groups, the 2 extra phosphates are released, releasing energy to make link the nucleotide to the new strand

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12
Q

What does PCR stand for?

A

Polymerase Chain Reaction

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13
Q

What is the purpose of the PCR technique?

A

To amplify quantities of a specific sequence of DNA from an initial minute sample

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14
Q

By what scale factor does the amount of DNA in a PCR replicate in every cycle?

A

It doubles

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15
Q

Describe the steps of PCR

A

Denaturation
Annealing
Elongation

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16
Q

Describe the step of denaturation in PCR

A

DNA sample is heated to 90* to separate 2 strands

17
Q

Describe the step of annealing in PCR

A

Sample is cooled (55*) to allow primers to anneal

18
Q

Describe the step of elongation in PCR

A

Sample is heated to the optimal temperate for a heat-tolerant polymerase (Taq) to function (75*)

19
Q

What is Taq polymerase

A

An enzyme used in PCR to extend the nucleotide chain from the primers so that they can be copied

20
Q

What is the optimum temperature of taq polymerase?

A

75* C

21
Q

Describe transcription

A

The process by which an RNA sequence is produced from a DNA template

22
Q

Function of RNA polymerase

A

Separates the DNA strands and synthesises a complementary RNA copy from on of the strand

23
Q

Why do the nucleotides involved in transcription have additional phosphate groups (ribonucleotide triphosphates)?

A

So that RNA polymerase can remove these phosphates to release the energy needed to covalently bond the nucleotides to the growing sequence

24
Q

What is the direction of transcription?

A

5’ - 3’

25
Q

What do we call the strand that is transcribed?

A

The antisense strand

26
Q

What do we call the strand that is not transcribed?

A

The sense strand

27
Q

Which strand is the RNA produced by transcription identical to?

A

The sense strand except the Thymine there is Uracil on RNA strands

28
Q

Where does transcription occur?

A

The nucleus

29
Q

Where does RNA go after transcription?

A

Cytoplasm (for translation)

30
Q

What does it mean that the genetic code is universal?

A

Almost every living organism uses the same code

31
Q

Why is a universal genetic code beneficial?

A

It allows species to transfer genes between species

32
Q

How do we produce insulin (via recombinant gene transfer)?

A

Take a human cell with an insulin gene
Insert it in a plasmid
Insert the plasmid in a transgenic bacteria
Grow in a culture and extract

33
Q

What is the start codon?

A

AUG