Genome evolution Flashcards

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1
Q

Transposons move around the genome. True or false?

A

True

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2
Q

Transposons are rare in the human genome. True or false?

A

False

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3
Q

Define a retrotransposon.

A

Transposons that replicate via an RNA intermediate using reverse transcriptase.

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4
Q

What is an LTR?

A

A long terminal repeat.

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5
Q

What produce LTRs?

A

Retroviruses with reverse transcriptase.

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6
Q

What is a LINR?

A

Long interspersed nuclear repeat.

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7
Q

What is used to transcribe LINRs?

A

Reverse transcriptase.

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8
Q

What is a SINR?

A

Short interspersed nuclear repeat.

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9
Q

Do SINRs use reverse transcriptase?

A

No.

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10
Q

Define a DNA transposon.

A

DNA is ‘cut and paste’ using transposase.

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11
Q

Selection tries to remove transposons. If there is no selection what happens?

A

Transposons accumulate.

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12
Q

Give 2 deleterious effects of transposons.

A
  1. Disrupt coding regions of DNA or regulatory sequences

2. Cause ectopic recombination, resulting in one chromosome with a deletion and one with a duplication.

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13
Q

There tend to be more insertions of transposons if…?

A

The rate of recombination is low.

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14
Q

Give 2 host mechanisms that control transposons.

A
  1. Transcriptional silencing

2. Post-transcriptional silencing

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15
Q

Explain transcriptional silencing.

A

Transcription is prevented via DNA methylation and chromatin modification.

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16
Q

Explain post-transcriptional silencing.

A

There is RNAi (interference) by Argonaute proteins and the enzyme Dicer, preventing translation of the RNA.

17
Q

A stable transposon rate in the genome is possible under what condition?

A

Rate of insertion is balanced by the rate of excision.

18
Q

Transposons are not the only cause of genome evolution. Give another.

A

WGD, thus leading to neo/subfunctionalisation etc.

19
Q

The loss of gene duplicates can be deleterious. How?

A

It causes less gene product to be produced, causing an imbalance. This is particularly true in protein networks.

20
Q

Duplicates are often retained. Why?

A

Genes that are highly expressed are preferentially selected for.

21
Q

What does CNV stand for?

A

Copy Number Variation.

22
Q

CNV is often implicated in disease. Why?

A

The amount of gene product is important to fitness.

23
Q

Genomes can evolve endosymbiosis. Give an example of this?

A

The mitochondria of eukaryotes used to be free-living alpha-proteobacteria.

24
Q

Why was endosymbiosis favourable for the mitochondria? Give 2 reasons.

A
  1. They are able to avoid Muller’s ratchet.

2. They can streamline their own genomes, making replication more energy efficient.

25
Q

Define CMS in plants.

A

Cytoplasmic male sterility: plants are hermaphrodite, but the mitochondria suppress male function, leading to pure females.

26
Q

Why does CMS exist?

A

The mitochondria and nuclear DNA have a conflict of interest. Mitochondria follow matrilineal inheritance and want to ensure they will be passed on to all the offspring. Nuclear DNA is inherited regardless of sex.

27
Q

What is a gynodioecious population?

A

A sexually dimorphic breeding population created by CMS whereby pure females and hermaphrodites coexist.

28
Q

Why does CMS harm nuclear gene transmission?

A

They are only passed on by the female and not the male parts.

29
Q

Define a nuclear restorer mutation.

A

One that has evolved to restore the hermaphrodite condition and thus male function in CMS.

30
Q

There has been co-evolution of the mitochondria and the nuclear genome. Why?

A

The mitochondria keep trying to dominate the nuclear genes, and the nuclear genes have to keep compensating.