Genetic Diversity: Mutations + Meiosis Flashcards

1
Q

What do gene mutations involve?

A
  • a change in base sequence of chromosomes
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2
Q

How do gene mutations arise?

A
  • spontaneously, during DNA replication + include base deletion + base substitution
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3
Q

Why don’t all base substitutions cause a change in sequence of encoded AAs?

A
  • bc of degenerate nature of genetic code
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4
Q

What can mutagenic agents do?

A
  • inc rate of gene mutation
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5
Q

How do mutations in NO° of chromosomes arise?

A
  • spontaneously, by chromosome non-disjunction during meiosis
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6
Q

What is chromosome non-disjunction?

A
  • when chromosomes or chromatids don’t split equally during anaphase
  • can occur in 2 forms: polyploidy or aneuploidy
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7
Q

What is polyploidy?

A
  • changes in whole sets of chromosomes + occur when organisms have 3 or more sets of chromosomes rather than 2
  • mainly occurs in plants
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8
Q

What is aneuploidy?

A
  • changes in NO° of individual chromosomes + occurs when individual homologous pairs of chromosomes fail to separate during meiosis
  • results in a gamete having 1 more or fewer chromosome
  • if this gamete is fertilised w a gamete w a normal NO° of chromosomes, zygote will have more or fewer chromosomes than normal, in all body cells
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9
Q

What does meiosis produce?

A
  • involves 2 nuclear divisions, so produces 4 haploid daughter cells, that are genetically diff from each other, from 1 diploid parent cell
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10
Q

What 2 mechanisms in meiosis introduce genetic variation among daughter cells?

A
  • independent segregation of homologous chromosomes
  • crossing over between homologous chromosomes
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11
Q

Describe how independent segregation of homologous chromosomes introduces genetic variation among daughter cells.

A
  • in meiosis 1, homologous pairs of chromosomes line up opposite each other at equator of cell
  • it’s random which side of equator paternal + maternal chromosomes from each homologous pair lie
  • pairs are separated, so 1 of each homologous pair ends up in daughter cell
  • this creates a large NO° of possible combinations of chromosomes in daughter cells produced
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12
Q

How do you calculate the NO° of possible diff combinations of chromosomes in a daughter cell produced, w/o crossing over?

A
  • 2^n
  • n = NO° of homologous chromosome pairs
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13
Q

Describe how crossing over between homologous chromosomes introduces genetic variation among daughter cells.

A
  • when homologous pairs line up opposite each other at equator in meiosis 1, parts of chromatids can become twisted around each other
  • this puts tension of chromatids, causing pairs of chromatid to break, which recombine w another chromatid, resulting in new combinations of alleles
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14
Q

Describe how meiosis differs from mitosis.

A

meiosis:
- 2 nuclear division, so produces 4 daughter cells
- produces haploid cells (1 set of chromosomes)
- creates genetic variation

mitosis:
- 1 nuclear division, so produced 2 daughter cells
- produces diploid cells (2 sets of chromosomes)
- creates genetically identical cells

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15
Q

How do you identify meiosis in a life cycle?

A
  • involves a diploid (2n) parent cell dividing, to become a haploid (n) cell
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16
Q

How is genetic variation within a species further inc?

A
  • random fertilisation of haploid gametes