Genetic Diversity due to Mutation and Meiosis Flashcards

1
Q

what is a frame shift

A

change resulting in misreading of all nucleotides downstream, usually resulting in a truncated non-functional protein

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2
Q

what type of mutations cause a frame shift and explain them

A

deletion - the removal of 1 or more bases resulting in a frame shift

addition - the adding of one or more bases resulting in a frame shift

duplication - where one or more bases is repeated causing a frame shift

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3
Q

what type of mutations don’t cause a frame shift and explain them

A

inversion - a sequence of bases is reversed e.g. TAGCAGCT becomes TCGACGAT

translocation - a sequence of bases is moved from one location in the DNA molecule to another part of the genome

substitution - the replacement of one or more bases by one or more different bases

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4
Q

why can a functioning protein still be formed after substitution

A
  • the DNA code is degenerate meaning that an amino acid can be coded by more than 1 base triplet
  • the mutation could have occured in an intron which doesn’t code for proteins
  • the mutation doesn’t affect the shape of the tertiary in a way that affects the function of the protein
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5
Q

difference between mitosis and meiosis (4)

A
  • mitosis has one nuclear division, meiosis does two
  • mitosis produces two daughter cells, meiosis produces four
  • mitosis produces genetically identical cells, meiosis doesn’t
  • mitosis produces cells with the same amount of chromosomes as the parent cell, meiosis produces cells with half
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6
Q

what is crossover during meiosis

A
  • the pair of homologous chromosomes lie side by side forming a bivalent
  • the chromatids of the homologous chromosomes then intertwine
  • the chromatids break and equivalent portions of the chromatids are exchanged
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7
Q

how is variation (genetic diversity) achieved during meiosis

A
  • independent segregation of homologous chromosomes
  • genetic recombination (crossover) within homologous chromosomes
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8
Q

how do you calculate the possible numbers of varied combinations of paternal and maternal chromosomes

A

2ⁿ

  • n = number of homologous pairs
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9
Q

what is independent segregation during meiosis

A
  • during the first meiotic division, hom. chromosomes pair together and then separate so that one member from each pair enters the gamete
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10
Q

what is a chiasma

A

site of crossing over

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11
Q

what is genetic recombination

A

the exchange of alleles ,during cross over, producing new combinations of alleles known as recombinants

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12
Q

what is nondisjunction

A

the failure of the chromosomes to separate during cell division , which produces daughter cells with abnormal numbers of chromosomes.

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