Mutations Flashcards

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1
Q

AT WHAT LEVELS CAN MUTATIONS OCCUR?

A
  1. genome mutation –> Change in chromosome number
  2. chromosomal mutations –> change in chromosomal structure
  3. point mutation –> Change in DNA sequence
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2
Q

in what cells can mutations occur in? what could the result be?

A
  • somatic cells –> Could result in cancer

- in germ-line cells –> Could result in gametes and offspring with mutations

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3
Q

what is the function of mutation in evolutionary change? what does mutation produce?

A

Ultimate source of evolutionary change
-Change in DNA sequence produces new alleles and allows for new combination of alleles to be passed
on to offspring

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4
Q

what are Spontaneous mutations?

A

naturally occurring mutations, arise in all cells without external cause

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5
Q

what are Induced mutations?

A

Induced mutations arise through the action of

certain agents called mutagens

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6
Q

what are the 2 basic types of genome mutation? what is the most common cause to the change in chromosome number?

A
  1. Changes in number of chromosome sets
  2. Changes in parts of chromosome sets = extra
    chromosomes or missing chromosomes

-Nondisjunction –> the failure of homologous chromosomes or sister chromatids to separate properly during cell division

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7
Q

what does Mitotic nondisjunction result in? what does it produce?

A

-in sections of the body having the wrong number of
chromosomes
-produces gametes with missing or extra chromosome(s) –> which Results in organisms with missing or extra chromosome(s)

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8
Q

what are the 4 major classes of chromosomal mutations?

A
  1. Chromosomal segment lost = deletion
  2. Chromosomal segment doubled = duplication
  3. Orientation of a segment within a chromosome
    reversed = inversion
  4. Segment moved to non-homologous chromosome = translocation
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9
Q

what is point mutation? where does it occur?

A
  • Change of a single base pair of DNA or a small number of adjacent base pairs
  • Can occur within a gene or between genes
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10
Q

what are the 2 main types of point mutation?

A
  1. Nucleotide Substitution = mutation in which one
    base pair is replaced by another
  2. Nucleotide Insertion or Deletion = mutation in
    which one base pair is added or deleted
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11
Q

what are 3 possible outcomes from substitution mutations in the protein-coding portion of a gene?

A
  1. Synonymous mutations = silent mutation
  2. Missense mutations = codon for one amino acid
    is changed into codon for another amino acid
  3. Nonsense mutation = changes codon into
    translation-termination (stop) codon
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12
Q

what do synonymous mutations (silent mutation) do?

A

-Mutation changes one codon for an amino acid into
another codon for the same amino acid

therefore Mutation in DNA does not change amino acid

Silent = no effect on amino acid sequence

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13
Q

what is a missense mutation? does it effect the proteins function?

A

Missense = results in a single amino acid change in the sequence
-Some missense mutations DO NOT affect the function
of the protein, such as:
1. the mutation is not in an important part of the protein
2. the mutation is a conservative substitution

-Some missense mutations DO change a protein’s
shape and ability to function

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14
Q

what is a conservative substitution? what is a non-conservative substitution? which is more likely to affect a protein’s structure and function?

A
  • replacing one amino acid with a chemically similar amino acid
  • this Alteration is less likely to affect protein’s structure and function severely

-amino acid replaced by chemically different amino acid
-this Alteration more likely to produce sever change in
protein’s structure and function

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15
Q

what do nonsense mutations do? what does it have an affect on? if a nonsense mutation is close to the end of the gene, it’s more likely to produce what? what do most nonsense mutations produce?

A

-Causes premature termination of translation
-Nonsense mutations can have considerable affect
on a protein’s structure and function

Nonsense = changes an amino acid codon into a stop codon

-more likely to produce a protein with some biological activity
-Most nonsense mutations produce completely
inactive protein products

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16
Q

what are Insertion and Deletion Mutations? what does it do to codons? what does it do to reading frame? when does this not happen?

A
  • Insertion or deletion of one or more nucleotide pairs
  • Changes all codons , and thus all amino acids, downstream of the mutation
  • Often changes reading frame –> “frameshift mutation”
  • Insertions or deletions in multiples of 3 base pairs does not cause a frameshift
17
Q

what can frameshift cause?

A

Frameshift can cause immediate nonsense (1 base-pair insertion) (termination)
Frameshift can cause extensive missense (1 base-pair deletion)
No frameshift, but one amino acid missing (3 base-pair deletion)