Mutations Flashcards

1
Q

What are mistakes in DNA replication referred to as?

A

Mutations

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2
Q

How does the cell prevent mutations in DNA replication?

A

It has an active repair system to correct damage in any DNA molecule

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3
Q

Give an example in which a mutation in a single nucleotide affects the performance of an organism

A

Sickle cell anaemia. There is a mutation in the beta-globin chain which cause sickle cells to be produced. Sickle-cell haemoglobin is less soluble than normal haemoglobin and forms fibrous precipitates.

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4
Q

A mutation in which cells cause the mutation to be passed on to offspring?

A

A mutation in the gametes. Any mutation in somatic cells will affect the individual but not the offspring.

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5
Q

What is the system which means that the number of DNA mutations is limited?

A

DNA mismatch repair

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6
Q

What is the probability of an error with the DNA mismatch repair system in place?

A

1 mistake in 10^9 nucleotides copied. Without the system in place, there is 1 mistake in 10^7 nucleotides copied.

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7
Q

What is another method of DNA becoming damaged and how?

A

Ultraviolet radiation. It promotes the covalent linkage of two adjacent pyrimidine bases e.g. thymine dimer

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8
Q

The three stages of DNA mismatch repair.

A
  1. Excision
  2. Resynthesis
  3. Ligation
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9
Q

Describe excision

A

The damage is cut out by a series of nucleases, each specialised for a type of DNA damage

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10
Q

Describe resynthesis

A

The original DNA sequence is restored by repair DNA polymerase which fills in the gap that was created by excision/

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11
Q

Describe ligation

A

DNA ligases seals the nick left in the sugar phosphate backbone of the repaired strand. Nick sealing requires energy from ATP hydrolysis remakes the broken phosphodiester bond between adjacent nucleotides.

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12
Q

What is the consequence of this DNA mismatch repair?

A

Because of the high accuracy, there are very similar sequences for closely related species.

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13
Q

How to determine the necessary fundamental sequences between two closely related species?

A

Compare them as far back as possible. A long time period.

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14
Q

What is the effect of homologous recombination?

A

It causes a change in DNA sequences

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15
Q

What is the requirement of the DNA molecules involved in homologous recombination?

A

Two double stranded DNA will have regions of similar DNA sequences.

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16
Q

The steps of homologous recombination

A

The similar sequences of DNA will align. The DNA molecules then “cross over”, both strands of each double helix are broken and then the broken ends are rejoined to the ends of the opposite DNA molecule to re-form two intact double helices, each made up of two different DNA molecules.

17
Q

Where is the site of exchange in homologous recombination?

A

The site of exchange can occur anywhere along the homologous nucleotide sequences in the participating DNA molecules

18
Q

Are the nucleotide sequences altered at the site of exchange?

A

No the nucleotide sequences are not altered at the site of the exchange. The cleavage and rejoining are so precise that a nucleotide is not gained or lost.

19
Q

What are the three forms of homologous recombination in bacterial cells?

A
  • Conjugation - direct cell-to-cell contact
  • Transduction - by a virus
  • Transformation - uptake, incorporation and expression of foreign genetic material
20
Q

What is a second type of recombination?

A

Site-specific recombination

21
Q

Describe site-specific recombination.

A

This involves mobile genetic elements. Short sequences of DNA can move from one position to another in the genome.

22
Q

What is the difference in bacteria between homologous and site-specific recombination?

A

There is no homology required between the end of the element and the insertion site.

23
Q

How has the diversity of species been affected by mutation?

A

The diversity has increased. It is a balance of the conservative accuracy of genome replication that enables progeny to develop virtues from their parents and the creative errors which allow them to develop novel features and evolve in capabilities.

24
Q

The five main types of gene mutation

A
  1. Mutation within a gene
  2. Gene duplication
  3. Gene deletion
  4. Exon shuffling
  5. Horizontal gene transfer
25
Q

What is mutation within a gene?

A

Mutations that change a single nucleotide, or delete or duplicate a nucleotide in the DNA sequence. They are ‘point’ mutations caused by failure in DNA repair after damage.

26
Q

What is gene duplication?

A

A large segment of DNA can be duplicated, creating a set of closely related genes within a single cell. The cell and the progeny of this cell, can use these duplicated genes to undergo additional mutations and assume functions distinct to those of the original gene.

27
Q

What is gene deletion?

A

Individual genes or whole blocks of genes are lost through chromosome breakage and failure to repair.

28
Q

What is exon shuffling?

A

Two or more existing genes can be broken and rejoined to make a hybrid gene containing DNA segments belonging to separate genes. Because this often occurs in intron sequences of eukaryotes, it doesn’t have to be precise.

29
Q

What is horizontal gene transfer?

A

A piece of DNA can be transferred from the genome of that cell to another.