2.7 DNA replication, transcription and translation Flashcards

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1
Q

What are the 3 proposed models for how DNA replicates?

A
  • Conservative
  • Semi-conservative
  • Dispersive
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2
Q

What happens in the conservative replication model?

A

The parental strands are kept together and the two newly synthesize daughter strands are kept together

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3
Q

What happens in the semi-conservative model of DNA replication?

A

Two daughter DNA molecules produced from the parent DNA molecule will each have one parental strand and one newly synthesized daughter strand.

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4
Q

What happens in the dispersive replication model?

A

Strands of the daughter DNA molecule contain pieces of parental and newly synthesize DNA. The original molecule breaks up into nucleotides, each one joins to a complementary nucleotide and new ones join up again.

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5
Q

What is the Meselson and Stahl experiment?
How did they culture 15N DNA?
What were they transferred in?
How did they measure?
What would happen?

A

They culture of the bacterium E. coli for 14 generations and a medium where the only nitrogen source was 15N. Therefore almost all the nitrogen atoms in the bases of the DNA in the bacteria were 15N.
- Then the bacteria was transferred to a medium in which all the nitrogen was 14N. They then collect the samples of DNA from the bacterial culture from time to time. They extracted the DNA and measured its density using density gradient centrifugation. The DNA solutions were spun at high speeds in a centrifuge. DNA molecules composed of heavy 15N would sink further in the solution than DNA molecule made of 14N.

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6
Q

What were the results of Meselson and Stahl.
Which models do the results support at generation 1? Why?
Which models do the results support at generation 2? Why?

A
  • After the bacterial population had doubled, the DNA band was midway between 15N and 14N bands.
  • Results show that DNA or hybrids with half heavy 15N nucleotides and half light 14N nucleotides. = DNA could have replicated either semi conservatively or dispersedly
  • after the bacterial population has doubled again, there were two DNA bands. One was lined up exactly with the 14N band and the other was at the midway point.
  • results show that one of the DNA strands contained only like 14N nucleotides. Does DNA therefore must have replicated semi conservatively.
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7
Q

What does topoisomerase (DNA gyrase) and DNA Helicase do?
What is DNA Helicase? What does it consists of?
What keeps the strands from reforming?
What is the result fo this process?

A

First topoisomerase unwind and release the strain on the double helix, a section at a time.
Than DNA Helicase enzyme follows behind, breaking H bonds between the bases.

DNA helicase is an enzyme consisting of 6 globular polypeptides arranged in a donut shape. One strand of the DNA passes through the center of the 5’ strand and the other strand passes outside of the enzyme.

Single stranded DNA binding protein (SSB) attaches to the bases of each nucleotide to separate the strands during replication so it doesnt reform.

Results in two single strand of DNA with exposed nucleotide bases.

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8
Q

How are nucleotides attached to the exposed bases in DNA replication?
What enzyme is involved? What strand does it read? In what direction?

A

DNA polymerase III reads the parent template strand in a 3’C to 5’C direction and builds the leading strand in a 5’C to 3’C direction.
DNA polymerase can only attach nucleotides to the free OH group on the 3’C.
DNA polymerase catalyses a condensation reaction that joins free phosphorylated nucleotides to exposed bases.

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9
Q

Where do free nucleotides come from?

A

Food - all food is derived from living organisms so it contains DNA which can be digested into its nucleotides which are stored in the nucleus of our cells

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10
Q

How is the lagging strand built?

A

They are built in opposite directions of the leading strand.
But it is also built in a 5’C to 3’C direction, away from the replication fork

It is built discontinuously in small sections know as Okazaki fragments

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11
Q

What does DNA ligase do?

A

It joins the Okazaki fragments together on the lagging strand

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12
Q

What does DNA primase in DNA polymerase I do?

A

DNA primase: attaches RNA nucleotides to a section of the template strand creating a double stranded attachment site for DNA polymerase III (which can only bind to double strands)

Polymerase I: removes the RNA nucleotides attached by the DNA primers from the newly synthesize strand and replace them with DNA nucleotides

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13
Q

Where in DNA molecules does DNA replication begin? How does eukaryotes and prokaryotes compare? Which way does replication occur?

A

Begins at sites called origins of replication.
In prokaryotes there’s one origin of replication.
In eukaryotes there are many origins of replication (replication bubbles) - replication occurs in both directions away from the origin.

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14
Q

What are energized/activated nucleotides? What are they called?

A

When nucleotides are phosphorylated and have 3 phosphate groups.
They are called nucleoside triphosphate (NTPs). Free nucleotides that bonds to the split original strands of DNA have 2 more phosphate groups than a normal nucleotide.
When DNA polymerase III comes to catalyse a condensation reaction to form phosphodiester bonds, hydrolysis of two phosphate molecules provide energize nucleotides which can be incorporated into the growing DNA strand by DNA polymerase III.

DNA - Deoxyribose = dNTPs
- dATP, dTTP, dCTP, dGTP

RNA - ribose = rNTPS
- rATP, rUTP, rCTP, rGTP

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15
Q

What are the steps of the PCR - The polymerase chain reaction?

A
  1. Denaturing - Dna sample is heated (95˚C) for 15 seconds to seperate the 2 strands by breaking the hydrogen bond
  2. Re-annealing - sample is cooled to 54˚C to allow primers to anneal for DNA polymerase III to bind - the primers designate the sequence to be copied
  3. Extension/Elongation - sample is heated to the optimum temperature for taq polymerase to function (72˚C)
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16
Q

What is taq polymerase?

A

Basically a substitute for DNA polymerase III because it can withstand the heat of the PCR

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17
Q

What is the PCR used for?

A

To make more of a specific DNA to analyze. Or to make more of one protein that is desired.

e.g. in a crime scene

18
Q

What is transcription?

A

the synthesis of RNA, using DNA as a template

19
Q

Outline the process of transcription

A
  1. The enzyme RNA polymeras binds to a site on the DNA at the start of a gene
  2. RNA polymerase moves along the gene separating DNA into single strands and pairing up RNA nucletides with complementary bases on one strand of the DNA
  3. Thymine is erplaces with uracil in RNA which pairs in a complementary fashion with adenine
  4. RNA polymerase forms covalent bonds between the RNA nucleotides
  5. The RNA separated from the DNA and the double helix reforms
  6. Transcription stop sat the end of the gene and the completed RNA molecule is released
20
Q

What is the product of transcription?

A

a molecule of RNA with a base sequence that is complementary to the template strand of DNA

21
Q

Which is the sense and antisense strand of DNA?

A

sense: same as RNA
antisense: acts as the template and has complementary base sequence to both the RNA and the sense strand

22
Q

What is translation?

A

the synthesis of polypeptide with an amino acid sequence determined by the base sequence of a molecule of RNA

23
Q

What does the ribosome consist of?

A

a small and large subunit, with binding sites for each of the molecules that take part in the translation

24
Q

What is mRNA?

A

RNA that carries the informatoin neeed to synthesise a polypeptide

25
Q

What does the pink and yellow, purple, green represent?

A

Pink and yellow: RNA molecules
Purple: proteins
Green: site that makes peptide bonds between amino acids, to link them together into a polypeptide

26
Q

what is tRNA involved in?

A

involved in decoding the base sequence of mRNA into an amino acid sequence during translation

27
Q

What is ribosomal RNA?

A

ribosomal RNA is part of the structure of the ribosome

28
Q

What is the genetic code?

A

the ‘translation dictionary’ that enables the cellular machinery to convert the base sequence on the mRNA into an amino acid sequence

29
Q

How many bases code for an amino acid?

A

3 bases
triplet code

30
Q

What is a codon?

A

a sequence of 3 bases on the mRNA

31
Q

How many possible codons are there?

A

64

32
Q

Why is the genetic code degenerate?

A

more than one triplet codes for each amino acid apart from Methionine (start codon) - reduce the effect of point mutations

33
Q

Why is the genetic code universal?

A

the same triplet codes for the same amino acids in every species

34
Q

Why is the genetic code non-overlapping?

A

each tirplet is distinct from the next

35
Q

What does the ‘stop’ codon code for?

A

end of translation

36
Q

What are amino acids carried on?

A

each by a specific tRNA, which has a three-base anticodon complementary to the mRNA codon for that particular amino acid

37
Q

What 3 components that work together to synthesize polypeptides by translation?

A
  • mRNA has a sequene of codons that specifies the amino acid sequence of the polypeptide
  • tRNA molecules have an anticodon of three bases that binds to a complementary codon on mRNA and they carry the amino acid corresponding to that codon
  • robosomes act as the binding site for mRNA and tRNAs and also catalyse the assembly of the polypeptide
38
Q

What is the summary of the main events of translation?

A
39
Q

What does the accuracy of translation depend on?

A

complementary base pairing between the anticodon on each tRNA and the codon on mRNA

40
Q

Why is it preferable to use human insulin?

A

because some diabetics develop an allergy to animal insulin

41
Q

What is human insulin produced with?

A

genetically modified E.coli bacteria

42
Q

How are we abl to use E.coli, yeast and fafflower to make human insulin?

A

because we share the same genetic code