Midterm 2 - Notes 3 (Part 1) Flashcards

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1
Q

What is molecular evolution mediated by?

A

Transposons

- but doesnt have to be

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2
Q

What are 4 major models of genetic innovations?

A
  1. Intragenic mutation
  2. Gene duplication
  3. DNA segment shuffling
  4. Horizontal transfer
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3
Q

What is the most common model for genetic innovations?

A

Intragenic mutations

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4
Q

Where do intragenic mutations occur?

A

Within protein coding regions

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5
Q

What happens with intragentic mutations?

A

Slightly changes the codon and possibly changes the function
- this occurs gradually

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6
Q

What is gene duplication?

A

Creates a 2nd copy that can be identical to the original gene in the genome

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7
Q

What does gene duplication allow?

A

Allows one copy to evolve while maintains the original function at the same time

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8
Q

What is DNA segment shuffling?

A

Mixing 2 parts of a genes in order to create a new gene

- contains parts of old genes in recombination

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9
Q

What is vertical transfer?

A

Transfer from one generation to the next in the same genome

- this is a slow process

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10
Q

What is horizontal transfer?

A

Transfer from one genome to another

  • this is a rapid process
  • novel function from distinct transfer
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11
Q

Exon shuffling

A

Is an evolutionary process for creating new genes form pre-existing ones by recombination between introns of 2 separated genes or by transposition of mobile DNA elements

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12
Q

Where are TE located via transposition of 2 integrated DNA transposons?

A

On either side of the gene (that wants to be cut out)

  • this is for translocation or duplication
  • its on either side the the exon for exon shuffling
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13
Q

What are cis elements needed for?

A

Expression and processing

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14
Q

What is transposition of a retrotransposon mediated by?

A

RNA transposon

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15
Q

Where are TEs located via transposition of a retrotransposon? (2)

A
  1. Upstream of the gene
    - gene duplication
  2. In an intron
    - exon shuffling
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16
Q

What does retrotransposons involve?

A

Run through transcription but utilizing the poly A signal on the TE

17
Q

What may or may not be included with retrotransposons?

A

Cis regulatory elements

18
Q

What does homologous recombination between TE not involve?

A

Transposition

- can use any type of TE

19
Q

What does homologous recombination between TE need?

A

TE

20
Q

Where are the 2 pairs of TEs of the same type located on 2 different genomic location?

A
  1. On either side of the gene
    - gene translocation
  2. On either side of introns
    - exon shuffling
21
Q

What does homologous recombination between TE involve?

A

Double cross over between identical TE sequences

22
Q

What is the problem in homologous recombination between TE?

A

The segments are very similar

23
Q

What do most proteins contain?

A

Multiple domains

24
Q

What can domain shuffling via transposons do?

A

Combine exons from distinct proteins

- can have a drastic effect on the new types of proteins

25
Q

What can combinations create?

A

New functions

26
Q

EGF

A

Epidermal growth factor

27
Q

What does an EGF initiate?

A

Signalling cascade

- binds to a receptor

28
Q

What does chymotrypsin do?

A

Its a protease (for digestion)

  • it cleaves peptide bonds
  • unspecific
29
Q

What does urokinase do?

A

It is a plasminogen activator

- it cleaves plasminogen and activates the formation of blood clods

30
Q

What does Factor IX(9) do?

A

It cleaves factor X(10)

- allows blood clod generation

31
Q

What does plasminogen do?

A

It cleaves fibrin

  • it dissolves blood clods
  • protein protein interaction domain
32
Q

What are retro-copies?

A

Copies of regular genes

- via transposition of “normal” cellular gene transcripts

33
Q

What may RT of non-LTR transposons act on?

A

May act on any RNA with a poly A tail
- binds and acts on a regular mRNA on the cell and brings it back into the cell and preforms RT and brings it into the genome

34
Q

What do retropsons (retro-copies) differ from?

A

Other gene duplicates

  • direct repeats and a poly A tail remainder
  • no introns because they would have been spliced out during RNA processing
  • no regulatory elements duplicated because they occur further upstream so they are not part of the duplication site and get a different expression pattern than the parent
35
Q

What are retro-copies prone to become? (2)

A
  1. Processed pseudogene

2. Neo-functionalization

36
Q

What are 4 things that are needed in order to become successful is a retro-copy?

A
  1. Needs to be inserted completely
    - needs to have a complete genome
    - needs to be downstream of the promoter so it gets duplcicated
  2. Must originate from a gene expressed
    - expressed in the germ line
  3. Must gain regulatory elements
    - needs a promoter and a terminator
  4. New regulatory modules must be advantageous
    - need an adaptive advantage to be able to be maintained
37
Q

Pseudogene

A

A section of a chromosome that is an imperfect copy of a functional gene
- evolves neutrally