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MICHELLE: Hi everyone.
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Welcome back.
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It's Michelle here again, and today, we're going to continue our discussion
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of meiosis.
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Today we'll be able to connect meiosis to Mendel's Law of Independent
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Assortment.
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Let's get started.
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OK.
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Here you see a diagram much like the ones that we saw in the previous
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video, except this one is a nucleus from a diploid cell with two different
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chromosomes.
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That means that 2n equals 4.
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Remember that this means that the organism contains
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four chromosomes total--
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two copies of the long chromosome and two copies of the short chromosome.
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Let's imagine that the red chromosomes were inherited from mom, and the blue
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chromosomes were inherited from dad.
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I'd next like you to assume that this individual has the genotype big A
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little a, big B little b.
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So we're going to consider the segregation of the alleles of two
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genes, the A gene and the B gene, for this example.
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Next imagine that this heterozygote had a mom whose genotype was big A big
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A, little b little b, and then dad, who had the genotype little a little
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a, big B big B. What does that mean?
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Well, that means that mom contributed big A and little b in her gametes, and
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dad contributed little a and big B in his gametes.
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OK.
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Next I'd like you to assume that the A and B loci are on different
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chromosomes.
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So given that information, I'd like you to take a minute, and with paper
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and pencil or through a computer or however you choose, recreate this
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figure for yourself and label the chromosomes with
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all the A and B alleles.
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Pause this video, and then we'll come back and work on it together.
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Great.
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Let's see how you did.
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So although we know that the A locus and the B locus are on different
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chromosomes, we don't know where on that chromosome.
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So for the purposes of this example, we're just going to pick a spot.
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But we do know that the red chromosomes are from mom, and the blue
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chromosomes are from dad.
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Remember that mom contributed big A. So let's just place big A allele here.
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If we look at the homologous chromosome that you got from dad, at
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the same locus, the allele is little a.
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Likewise, let's imagine that this is the locus for the B gene.
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Mom contributed a little b allele.
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And at the same locus on the homolog, dad contributed the big B allele.
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Great.
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So now I'd like you to pause the video for a minute and trace these alleles
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through every stage of meiosis.
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What's the genotypes of the gametes that you get?
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Excellent.
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Let's go through this together.
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So the first step of meiosis is replication, and so here we have the
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replicated chromosomes.
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And remember that sisters are pretty much copies of each other, so if you
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placed the alleles on the replicated chromosomes, it's going to look
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something like this.
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OK.
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Great.
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So now the next step, again, is recombination.
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After recombination occurs, the chromosomes align in meiosis I. So I'm
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going to show that here.
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OK.
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So here we are in metaphase I, and I'm just going to quickly place the
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alleles on this diagram.
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I'm going to label both sisters at once for simplicity.
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Is this the only way that the chromosomes can align in metaphase I?
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Is there a specific reason why I put the red chromosomes on the left side
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and the blue chromosomes on the other?
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There's not.
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The alignment of chromosomes in metaphase I is random.
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And that means that here is one possible
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configuration, but there's another.
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Chromosomes can also align like this at metaphase I. In this alignment, the
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alleles will look like this.
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What does this mean for meiotic chromosome segregation?
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Let's first take a look at the meiosis on the left panel.
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So homologous chromosomes segregate in meiosis I, and sisters split in
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meiosis II.
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And so you get two types of gametes--
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gametes with a little b big A genotype or a little a big B genotype, like so.
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So now what does this mean for meiosis if chromosomes align in the other way?
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And so that I'm showing here.
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Let me just take a minute to place the alleles.
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And now sisters split in meiosis II.
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So if chromosomes align like this, you'll get gametes of genotype big A
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big B and little a little b.
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So in this population of gametes, you would expect equal frequencies of
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these genotypes--
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big A little b, little a big B, big A big B, and little a little b.
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Now let's think about a Punnett square for a dihybrid cross, where one of the
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individuals has genotype big A little a and big B little b.
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So we write that the four combinations of gametes would look like this, and
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now we can understand why this would be.
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If chromosomes align in the orientation on the left, you get big A
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little b and little a big B, which correspond to these two gametes.
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But in the other half of the population, you'll align in the other
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orientation and get out gametes that have genotype big A big B and
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little a little b.
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And these will come out at equal frequencies when the genes are located
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on different chromosomes and, therefore, assort independently.
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So to predict all the possible gametes when considering three or more genes
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becomes very complicated.
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And when you consider the thousands of genes that humans have on their 23
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pairs of chromosomes, it becomes easier to understand why siblings can
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appear very different from each other.
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Great work, everyone.
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We've gone through so many concepts already.
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And hopefully now you understand the connection between meiosis and
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Mendel's Law of Independent Assortment.
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See you next time.
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