Topic 1 Flashcards

1
Q

What experiment did Griffith do in 1928?

A

First experiment suggesting that bacteria are capable of transferring genetic information through a process known as transformation.

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2
Q

What experiment did Avery do in 1944?

A

Found out that it is DNA that is the transforming agent

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3
Q

What experiment did Hershey and Chase do in 1952?

A

Radioactively labelled isotopes (phosphate and sulphur to show that it is DNA and not protein that contains genetic material.

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4
Q

How many bonds do a) AT b) CG form

A

AT form Two ; CG form 3

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5
Q

In what direction does DNA run?

A

DNA template is read in 3’ to 5’ direction BUT a new strand is synthesized in the 5’ to 3’ direction.

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6
Q

Meselson and Stahl experiment

A

Worked out DNA replication is semi-conservative.

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7
Q

Role of DNA primase

A

DNA primase: lays down a short strand of RNA to act as a primer for DNA synthesis (DNA primase is an RNA polymerase) . So Ozakaki fragments can form

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8
Q

Role of DNA polymerase I

A

DNA polymerase I: This enzyme synthesizes new DNA strands on the lagging strand and during DNA repair

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9
Q

Role of DNA polymerase III

A

DNA polymerase III: This enzyme synthesizes new DNA strands on the leading strand

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10
Q

Role of single stranded binding proteins

A

Single stranded binding proteins: These proteins bind to single stranded DNA at the replication fork to stabilize the single strands (ie stop them reannealing)

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11
Q

Role of DNA helicase

A

DNA helicase: This enzyme unzips the two strands of DNA at the replication fork.

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12
Q

What are Okazaki fragments

A

The short fragments of DNA synthesized on the lagging strand of DNA as the replication fork progresses.
They contain an RNA primer. The primer is subsequently removed by DNA polymerase I (or eukaryotic equivalent) and fragments joined by DNA ligase.

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13
Q

How does the DNA polymerase reduce the frequency of errors from 1 in 105 to 1 in 107?

A

The polymerase has a 3′ to 5′ proofreading activity that checks if the correct base has been inserted before the next base is inserted. If an error has been made, the base is excised and replaced. The accuracy of this proof reading is 1 error in 100 base insertions.

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14
Q

Role of DNA ligase during DNA repair

A

Joins fragments of DNA together (eg Okazaki fragments on the lagging strand, or newly synthesized DNA strands during repair of DNA).

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15
Q

Function of uracil N-glycosylase. How’s this help reduce mutation in DNA

A

Uracil-N-glycosylase cuts (excises) uracil from DNA.
Uracil can arise in DNA by the deamination of cytosine. If the uracil is not removed it will base pair with adenine during replication, resulting in a C to T mutation (also called GC to AT if giving the base on both strands of the DNA).

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16
Q

How many base pairs of DNA

A

About 3 billion base pairs in the whole sequence (or 6 billion altogether).

17
Q

In Sanger DNA sequencing how is the growing chain of DNA terminated?

A

When a dideoxynucleotide (ddNTP) is inserted; as it has no free 3′-OH group, the polymerase cannot continue adding bases.

18
Q

What is needed in each reaction mix for Sanger sequencing?

A

The polymerase enzyme, a gene specific primer, all four dNTPs, one specific ddNTP

19
Q

Define polymorphism

A

A sequence variation that occurs in at least 1% of the population.

20
Q

SNP

A

Single nucleotide polymorphism

21
Q

Define: DNA microarray

A

An array of thousands of different DNA sequences laid out in a grid on a microchip (glass slide)

22
Q

Give 2examples of what microarrays could be used to investigate.

A

Occurrence of different SNPs in an individual

Differences in gene expression between eg different samples, tumour vs normal tissue, etc.

23
Q

Is the mRNA a replica of the sense or anti-sense strand of DNA?

A

The sense strand (ie carries the message). Makes sense…

24
Q

Which enzyme carries out transcription?

A

RNA polymerase (forms mRNA)

25
Q

3 mRNA modifications

A

5′- cap, polyA tail, splicing out introns.

26
Q

Define intron and exon

A

Introns: non-coding sequences in DNA (e.g. remain in the DNA)
Exon: coding parts of the gene that are transcribed into protein

27
Q

Which a.a. is always 1st

A

Methionine (AUG) (STOP codons are UAG, UGA, UAA)

28
Q

Which end of tRNA molecule is a.a attached

A

3’ end (just as the free OH- group is on the 3’ end of DNA)

29
Q

Role of A, P and E sites on ribosome

A

A: newly arrived tRNA docks in the A site
P: growing polypeptide is attached to the tRNA in P-site
E: after next polymerisation reaction, uncharged tRNA moves to E site and exits

30
Q

3 antibiotics that target prokaryotic ribosomes

A

tetracycline, streptomycin and chloramphenicol

31
Q

What are monoamine oxidase inhibitors treat?

A

Depression

32
Q

Experiment where AT go together

A

Erwin Chargaff (1952)

33
Q

Barr body

A

the inactive X chromosome in a female somatic cell, rendered inactive by a process called lyonization

34
Q

What are pseudogenes

A

non-functional genes

35
Q

What is a TATA box?

A

run of T and A bases. Region of the promoter where transcription factors bind to initiate transcription by binding the RNA polymerase to the region of the gene where transcription begins.

36
Q

Transcripts are…

A

capped, spliced, polyadenylated and then exit the nucelus.

37
Q

What is polyadenylation

A

Polyadenylation is the addition of a poly(A) tail to a messenger RNA. The poly(A) tail consists of multiple adenosine monophosphates; in other words, it is a stretch of RNA that has only adenine bases. In eukaryotes, polyadenylation is part of the process that produces mature messenger RNA (mRNA) for translation.