Mutations lectures (2) Flashcards

1
Q

why are bacteria good model systems?

A
  • unicellular (change in phenotype WILL affect that cell)
  • single chromosome - haploid - no competing alleles
  • replicate by binary fission
  • > all daughter cells identical to parent
  • > no genetic variation
  • simple gene structure
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2
Q

Stop codons

A

UAA, UAG, UGA

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3
Q

mutants in bacteria

auxotrophs

A

amino acid/vitamin

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4
Q

mutations in bacteria

resistance

A

antibiotics/phage/toxic chemicals

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5
Q

mutations in bacteria

inability to use a substrate

A

sugar

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6
Q

non-selective media

A

all cells grow so test individual colonies

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7
Q

selective media

A

e.g. antibiotic present / absence of amino acid

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8
Q

indicator media

A

e. g. MacConkey Agar

- identifies whether bacteria use lactose

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9
Q

silent mutation

A

different codon, same amino acid

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10
Q

missense mutation

A

different amino acid, different protein

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11
Q

nonsense mutation

A

changes to stop codon, cuts protein short

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12
Q

frame-shift mutation

A

adds/removes nucleotide, shifts sequence

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13
Q

deletions

A

removes genes, may change phenotype

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14
Q

insertions

A

adds gene(s), may change phenotype

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15
Q

rearrangements

A

reorders gene (s), may not change phenotype

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16
Q

point mutations

A

affect one single gene

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17
Q

types of point mutations

A
  • silent mutations
  • missense mutations
  • nonsense mutations
  • frame-shift mutations
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18
Q

types of larger-scale mutations

A
  • deletions
  • insertions
  • rearrangements
19
Q

reverse and suppressor mutation types

A
  • forward mutation

- reversion

20
Q

what is a forward mutation?

A

wild type sequence -> mutant sequence

21
Q

what is a reversion mutation?

A

1) reverse
mutant sequence -> wild type sequence

2) suppressor
mutant sequence

22
Q

Types of reversion mutation

A
  • reverse

- suppressor

23
Q

Mutation Rate formula

A

= ratio in a population of (number of mutants/number of wild types)

24
Q

requirements for measuring frequency of mutation

A

large populations

special techniques

25
Q

Induced mutations are caused by…

A

mutagens and radiation

26
Q

transition mutations

A

pyrimidine -> pyrimidine

purine -> purine

27
Q

transversion mutations

A

pyrimidine -> purine

purine -> pyrimidine

28
Q

why are transition mutations more common than transversion mutations?

A

pyrimidines and purines (two rings) are more structurally different from each other than within their group.

29
Q

Spontaneous mutations

A

independent of selective (dis) advantage to host
each gene mutates at a characteristic rate
each type of mutation occurs at a characteristic rate

30
Q

Base Analogues

A

molecule similar to one of the four DNA bases

31
Q

Base analogues incorporated into DNA…

A

ONLY at replication

32
Q

Base analogues can…

A

pair with a normal base

33
Q

Example of a base analogue to thymine

A

5 - bromouracil

34
Q

nitrous acids causes what type of mutations?

A

transitions A-T -> G-C

35
Q

alkylating agents cause what type of mutations?

A

transition A-T -> G-C

36
Q

Intercollating chemicals

A

planar, ringed molecules the size of a base pair (bp)

37
Q

examples of intercollating chemicals

A

acridine

ethidium bromide

38
Q

order these mutations in their ease to be fixed and tolerance to mutation by radiation

  • ssDNA breaks
  • nucleotide substitution
  • dsDNA breaks
A
  • nucleotide substitution
  • ssDNA breaks
  • dsDNA breaks
39
Q

DNA repair mechanisms

A
Apurine gap repair
Mismatch pair 
Photoreactivation repair 
Excision repair 
Post-replication repair
40
Q

Apurine gap repair

A

uses AP endonuclease
- removed damaged base
- ss gap filled by polymerase
if no repair inserts A

41
Q

Mismatch pair

A

nearby ss cut and excision of ssDNA past mismatch

DNA polymerase repairs gap

42
Q

Photoreactivation repair

A

light driven process

various enzymes with specific properties

43
Q

Excision repair

A

multi-enzyme system
enzymes identify & instant removal
polymerase repairs

44
Q

Post-replication repair

A
polymerase can't replicate across damaged DNA, leaves gap
gap filled by strand exchanged from another dsDNA
secondary gap (from where strip take - not damaged) repaired by polymerase