Mitosis and Meiosis 2 Flashcards

1
Q

Describe Human Chromosomes

A
  • Humans have 22 autosomal chromosomes, 1 pair of sex determining (23 total)
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2
Q

Homologous chromatids

A
  • result of obtaining one set of chromosomes from the male and one from the female parent
  • contain the same set of genes that may differ slightly in sequence
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3
Q

Prophase I

A
  • pairing of homologous chromosomes, key difference between meiosis and mitosis
  • structure called a tetrad
  • has crossover
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4
Q

Metaphase I

A
  • tetrads within middle of cell
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5
Q

Anaphase I

A
  • each set of chromosomes migrate to opposite poles
  • NOT sister chromatids, they are not identical anymore from crossing over
  • each pair has 1 chromatid untouched, and that crossed over (both sides must receive a set of small, medium, and large)
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6
Q

Telophase I

A
  • cells with the same DNA content but not identical genomes
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7
Q

Prophase II

A
  • crossover DOES NOT OCCUR
  • not true sister chromatids
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8
Q

Metaphase II

A
  • chromatids line up at metaphase plate
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9
Q

Anaphase II

A
  • chromatids are separated with each chromatid pulled to opposite poles
  • both receive equal amounts of DNA
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10
Q

Telophase II

A
  • results in 4 cells each with half the chromosomes as the original cell
  • notice each cell has a unique genome!!
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11
Q

Nondisjunction

A
  • chromatids fail to separate (in anaphase I or II, errors in meiosis)
  • results in gametes and zygot with abnormal chromosome number
  • Aneuploidy: variations in chromosome number that involve one or more chromosomes
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12
Q

Nondisjunction in Anaphase 1 vs 2

A
  • this mechanism will create bigger defects in anaphase I over anphase II, because chromosomes will not be spread evenly over two cells instead of one
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13
Q

Normal Sex Chromosomes

A
  • X Y, normal male
  • XX, normal female
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14
Q

Klinefelter syndrome

A
  • female nondisjunction, XX–Y
  • meiosis I, X–XY
  • 47 chromosomes
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15
Q

Turner syndrome

A
  • female nondisjunction, –X
  • male nondisjunction, X–
    -meiosis II, X–
  • 45 chromosomes
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16
Q

Jacobs Syndrome

A
  • meiosis II
  • X–YY
  • 47 chromosomes
17
Q

Aneuploidy

A
  • an extra or missing chromosome
18
Q

Monosomy

A
  • one chromosome absent
19
Q

Trisomy

A
  • one chromosome extra