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How would you define a chromosome?
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What do you picture in your head?
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In eukaryotes, a chromosome consists of a single molecule
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of DNA associated with proteins that help maintain
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its structure and function.
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You've probably seen a chromosome depicted like this.
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However, this commonly used image
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can be misleading, as it actually
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depicts a linked pair of identical sister
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chromatids after DNA replication.
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A single condensed chromosome actually
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should be depicted like this.
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This is one of several instances where imperfect terminology
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can make biological processes seem
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more puzzling than they actually are.
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So in this video, we will give an overview
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of a few important terms and concepts
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that are used throughout biology.
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Every human cell has a mass of DNA associated
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with other proteins and RNA stored in the nucleus.
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We call this complex of macromolecules chromatin.
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You may have heard chromatin described as a tangled
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mess of DNA and protein, but we're
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starting to figure out that it does actually
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have its own organization.
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Each chromosome contains a single molecule
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of DNA associated with proteins to help
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it maintain its structure and function.
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Chromosomes can be un-condensed or condensed.
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The compact structure of a condensed chromosome
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allows the cell to more easily move and manipulate chromosomes
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independently, which is useful for cellular processes
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like mitosis and cytokinesis.
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Humans have 23 unique chromosomes,
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each including the proteins associated
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with a single molecule of DNA containing
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many genes, regulatory elements, and non-coding DNA.
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Biologists quantify this number of unique chromosomes
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in an organism-- also known as the number of chromosomes
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in a haploid cell, such as ovum or sperm in humans--
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with the variable N. Therefore, we
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say that human cells have N equals 23.
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n changes between species and does not
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indicate how complex the organism is.
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For example, the cells of budding yeast--
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Saccharomyces cerevisiae-- have n equals 16.
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The cells of fruit flies-- Drosophila melanogaster--
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have n equals 4, while the cells of domestic dogs-- Canis
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familiaris-- have N equals 39.
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Even though humans have 23 unique chromosomes
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in each haploid cell, our somatic, non-sex cells
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are diploid.
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So in most of our cells, we have two slightly different sets
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of these unique chromosomes.
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Therefore, we describe diploid cells
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as 2N, or as having 46 chromosomes in total.
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You receive one set of 23 chromosomes from your mom
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and one set of 23 chromosomes from your dad.
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These chromosomes contain various similar sequences
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of DNA, but have different versions
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of the same gene located in the same spot, or locus on the DNA.
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We call these different versions of the same genes alleles.
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Also, because these chromosomes are very similar
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but don't contain identical DNA sequences,
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we call them homologous chromosomes.
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Same-- homo, relation-- logos.
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In some, there are two types of cells in humans
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and many eukaryotes-- haploid and diploid.
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Haploid cells have one unique copy
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of each chromosome-- for example, N equals 23 in humans.
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Diploid cells have two copies of homologous chromosomes--
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for example, 2N equals 46 in humans.
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So what happens to our DNA and chromosomes
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when we have to make more cells through cell division?
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The series of biological events that occur during each cell
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division is called the cell cycle.
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In this video, we will focus on the mitotic cell cycle
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with cells that undergo mitosis to create two daughter cells.
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When a human cell undergoes replication,
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every single one of our 46 homologous chromosomes
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is duplicated to form identical pairs.
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Each member in an identical pair of chromosomes
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is called a sister chromatid.
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Each sister chromatid is just a copy of one of 46 homologous
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chromosomes, and they are linked together into one unit.
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This is where you may have heard some people describe
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the cell as having four N chromosomes, which
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can be misleading.
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These cells are still diploid with 2N, or 46, homologous
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chromosomes.
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Even though they are currently duplicated
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as pairs of sister chromatids, you
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didn't receive two more sets of new homologous chromosomes
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with different alleles, and the amount of unique chromosomes
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has not increased.
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Instead, you can describe this cell
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as diploid with two N chromosomes and 4C DNA content.
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The C value stands for constant-- the genome size
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or amount of DNA that is characteristic
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of a particular haploid cell.
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As such, a haploid cell will have 1C DNA content,
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and a diploid cell that hasn't undergone DNA replication
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will have 2C DNA content.
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This specific terminology allows us
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to describe how the diploid cell that
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has undergone DNA replication still has
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only two sets of homologous chromosomes-- 2N--
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but now contains 4C DNA content.
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That is, this cell contains twice the DNA content it once
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had-- 2C-- because each chromosome has been replicated
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to form a pair of sister chromatids.
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This DNA replication ensures that at the end of each cell
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cycle involving mitosis, the cell
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can split these pairs of sister chromatids apart to divide
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into two diploid daughter cells with 2N chromosomes and 2C DNA
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content.
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Hopefully, now you can explain the difference
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between chromatin and chromosomes
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and can describe how the homologous chromosomes
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duplicate to form pairs of sister chromatids
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when the cellular DNA is replicated.
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These concepts and their vocabulary
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are tricky, but are very useful to understand thoroughly
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when talking or thinking about biology.
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Thanks for watching.
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