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MICHAEL HEMANN: Errors do occur.
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And errors in meiotic chromosome segregation
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are called non-disjunction events, non-disjunction meaning
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that there is some error in the segregation
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of these chromosomes.
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So let's think about what happens if there's actually
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a non-disjunction event, so an abnormal
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or an aberrant segregation.
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So what happens if you actually get
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all of these chromosome ones that actually all
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go in one direction?
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After meiosis I, we have two progeny.
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One of the progeny has the two homologs present,
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and the other progeny has nothing.
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So they've all segregated all of their chromosome
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Is into one target cell.
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So as this goes into meiosis II, we have the four gametes.
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And in the four gametes, you have the two homologs present.
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So you're going to end up with two gametes that
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have two times as many-- or as much chromosome
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I as they should normally have.
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So they're going to enter fertilization
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bringing two copies of a particular chromosome.
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So this is characteristic of a meiosis I non-disjunction
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event.
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Now you can think of a meiosis II non-disjunction event.
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So if you have a meiosis II non-disjunction event starting
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from that cell there, the result is you have two gametes,
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and one of these gametes will have two copies of chromosome I
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and no copies of the other chromosome.
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Or, the other gamete will have no chromosome I copies.
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There's actually a distinction, a major distinction
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between these, and it allows you to recognize
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the difference between a meiosis I and a meiosis II
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non-disjunction event.
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So in a meiosis I non-disjunction event,
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you actually have the two homologs
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that are present in the final germ cells.
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So these are two distinct chromosomes.
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One is maternal, one is paternally derived.
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In a meiosis II non-disjunction event,
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you have two sister chromatids that are present.
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And so when we learn about DNA markers,
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we're going to be able to discriminate
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between a meiosis I and a meiosis II
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non-disjunction event based on the origin of the chromosomes
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that are inherited.
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