Genetics of living systems chp 19 DONE THIS ON OTHER DECK Flashcards

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1
Q

what is a mutation when talking about DNA

A
  • a change in the sequence of bases in DNA
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2
Q

what are the 3 difference types of change in the sequence of DNA bases

A
  • substitution
  • deletion
  • insertion
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3
Q

what is it called when only one nucleotide is affected by mutation

A
  • point mutation
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4
Q

what is meant when the genetic code is called degenerate

A

a single amino acid may be coded for by more than one codon.

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5
Q

what does the substitution of a single nucleotide change

A

the codon in which it occurs

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6
Q

what type of mutation does insertion and or deletion cause

A

frameshift mutation

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7
Q

define reading frame/triplet code

A
  • way of dividing sequence of nucleotides in a nucleic acid molecule (RNA/DNA) into codons
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8
Q

how does insertion/deletion cause frameshift

A

it moves/shifts the reading frame of the sequence of bases.
^this will change every successive codon from the point of the mutation

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9
Q

under what conditions could insertion/deletion not result in frameshift

A
  • if the number of nucleotides added or deleted are multiples of 3
    ^as they would correspond to full codons and the reading frame would not be changed
  • ^the protein formed will still be affected as an amino acid is added or deleted
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10
Q

what are the effects of different mutations

A
  • no effect - because normally functioning proteins are still synthesised
  • damaging - organism affected in negative way because proteins are no longer synthesised or proteins synthesised are non-functional
  • beneficial - very rare, protein synthesised results in new and useful characteristics in phenotype.
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11
Q

what is a mutagen

A

a chemical, physical or biological agent which causes mutations

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12
Q

what is the loss of purine and pyrimidine bases called

A
  • loss of purine base is called depurination
  • loss of pyrimidine base is called depyrimidination
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13
Q

how can the absence of a base lead to insertion

A

can lead to insertion of an incorrect base through complementary base pairing during DNA replication

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14
Q

how can free radicals cause mutations

A
  • can affects the structure of nucleotides
  • disrupt base pairing during DNA replication
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15
Q

what’s the difference between gene and chromosome mutations

A

gene mutations occur in single genes or sections of DNA whereas chromosomes mutation affect the whole chromosome or number of chromosomes within a cell

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16
Q

what are some ways that chromosomes can mutate

A
  • deletion - a section of chromosome breaks off and is lost within the cell
  • duplication - sections get duplicated on a chromosome
  • translocation - a section of one chromosome breaks off and joins another non-homologous chromosome
  • inversion - a section of chromosome breaks off, is reversed and then joins back onto the chromosome
17
Q

define codon

A
  • set of consecutive, non-overlapping triplets in a nucleic acid molecule (RNA/DNA)