Unit 2: DNA Mutations Flashcards

1
Q

point mutation (nucleotide substitution) (2)

A
  • mutation where a base pair is replaced by a different base pair
  • the most frequent type of mutation
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2
Q

single-nucleotide polymorphism (SNP) (2)

A
  • site in the genome where the base pair that is present differs among individuals in a population
  • result of point mutation
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3
Q

why do many point mutations have no detectable effects on the organism?

A
  • they occur in noncoding DNA
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4
Q

synonymous (silent) mutation

A
  • mutation resulting in a codon that does not alter the corresponding amino acid in the polypeptide
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5
Q

amino acid replacement

A
  • change in the identity of an amino acid at a particular site in a protein resulting from a mutation in a gene
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6
Q

non-synonymous (missense) mutations

A
  • point mutation that causes an amino acid replacement
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7
Q

nonsense mutation (2)

A
  • mutation that creates a stop codon, terminating translation
  • nearly always has harmful affects as they are nonfunctional, unstable and quickly destroyed
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8
Q

what happens when a deletion or insertion occurs in a noncoding DNA?

A
  • mutations have little or no effect
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9
Q

What happens when deletion or insertion occurs in groups of 3 nucleotides?

A
  • deletion or addition of amino acids in the resulting polypeptide chain results
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10
Q

what happens when deletions and insertions occur that are not in exact multiples of 3?

A
  • can cause major changes in the amino acid sequence because they do not delete or insert entire codons
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11
Q

frameshift mutations (2)

A
  • mutation in which an insertion or deletion of some number of nucleotides that is not a multiple of 3 causes a shift in the reading frame of the mRNA changing all following codons
  • mutant protein does not fold properly into its tertiary structure and becomes nonfunctional
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12
Q

wild-type

A
  • the natural state of an organism isolated in nature (“in the wild”)
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13
Q

genotype

A
  • the hereditary (genetic) information within an organisms genome
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14
Q

phenotype

A
  • resulting expression of the genotype within an organism resulting in observable traits
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15
Q

mutant

A
  • an organism with a changed genotype, usually in a specific location in the DNA
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16
Q

mutation

A
  • change in the genotype
17
Q

what can mutations arise from?

A
  • incorrect DNA copying during replication
  • chemical mutagens
  • environmental damage
18
Q

A missense point mutation changes a base in the template strand only, how will this change phenotype?

A
  • in the current cell and one of the daughter cells