WEBVTT - Why Do Most People Have 46 Chromosomes?

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<v Speaker 1>Welcome to brain Stuff, a production of iHeart Radio. Hey

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<v Speaker 1>brain Stuff, Lauren Bogel bum here. You may have heard

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<v Speaker 1>that a hundred and thirty seven is the magic number,

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<v Speaker 1>but if you ask a geneticist, they'll tell you that

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<v Speaker 1>the real magic is in forty six. Why forty six

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<v Speaker 1>because that's the total number of chromosomes found in most

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<v Speaker 1>every human cell, twenty three pairs to be exact, and

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<v Speaker 1>those little red like structures pack all the information about

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<v Speaker 1>who you are and what makes you unique. To understand

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<v Speaker 1>what chromosomes are, first, we have to understand what DNA is.

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<v Speaker 1>Formally known as de oxy ribonucleic acid, DNA is a

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<v Speaker 1>complex molecule found in all plants and animals. It's found

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<v Speaker 1>in almost every cell of an organism's body, and it

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<v Speaker 1>contains all of the information necessary to keep that organism

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<v Speaker 1>up and running and developing and reproducing. DNA is also

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<v Speaker 1>the primary way that organisms pass on hereditary information and

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<v Speaker 1>the access of reproduction. A portion of DNA is passed

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<v Speaker 1>along from parent to offspring. In short, DNA is what

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<v Speaker 1>tells the story of your totally unique biology. As you

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<v Speaker 1>can probably imagine, DNA has to be pretty long to

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<v Speaker 1>hold all of that important information, and it is. If

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<v Speaker 1>you stretched the DNA and just one cell all the

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<v Speaker 1>way to its full length, it would be about six

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<v Speaker 1>and a half feet or two meters long. And if

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<v Speaker 1>you put the DNA and all your cells together, you'd

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<v Speaker 1>have a chain about twice the diameter of the solar system. Luckily,

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<v Speaker 1>cells are pretty smart and have an ingenious way of

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<v Speaker 1>packaging all that info into space efficient parcels. Enter the chromosome,

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<v Speaker 1>with its name rooted in the Greek words for color

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<v Speaker 1>chroma and body soma. The chromosome is a cell structure

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<v Speaker 1>or body that scientists can spot under a microscope by

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<v Speaker 1>staining it with colored dyes and get it. Each chromosome

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<v Speaker 1>is made up of protein and YEP d n A.

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<v Speaker 1>Every chromosome contains exactly one molecule of DNA to be exact,

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<v Speaker 1>and that long string of genetic info is tightly wrapped

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<v Speaker 1>around the protein called a his stone, which acts like

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<v Speaker 1>a spool, efficiently bundling the lengthy info rich molecule into

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<v Speaker 1>the perfect size and shape to fit inside the nucleus

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<v Speaker 1>of a cell. Human cells typically have twenty three pairs

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<v Speaker 1>of chromosomes for a total of forty six aside from

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<v Speaker 1>sperm and egg cells, which each contain only half of

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<v Speaker 1>that that's twenty three chromosomes. The magic number of forty

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<v Speaker 1>six or twenty three pairs of chromosomes per cell isn't

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<v Speaker 1>universal among living things. Of first, humans happen to be

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<v Speaker 1>a diploid species, which means that most of our chromosomes

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<v Speaker 1>come in matched sets called homologous pairs. The two members

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<v Speaker 1>of each pair are called homologus. A lot of animals

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<v Speaker 1>and plants are diploid, but not all of them have

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<v Speaker 1>a total number of forty six chromosomes. Mosquitoes, for example,

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<v Speaker 1>have a diploid chromosome number of six, frogs have twenty six,

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<v Speaker 1>and to shrimp have a whopping five hundred and eight chromosomes.

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<v Speaker 1>But why do humans have twenty three pairs? It happened

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<v Speaker 1>during evolution. For the article, this episode is based on

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<v Speaker 1>How Stuff Works. Spoken by email with Berlin Hurley, PhD,

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<v Speaker 1>a research fellow at the National Human Genome Research Institute

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<v Speaker 1>at the National Institutes of Health. She said humans have

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<v Speaker 1>twenty three pairs of chromosomes, while all other great apes, chipanzees,

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<v Speaker 1>Bonnabo's guerrillas, and orangutans have twenty four pairs of chromosomes.

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<v Speaker 1>This is because in the human evolutionary lineage, two ancestral

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<v Speaker 1>ape chromosomes fused at their telomeres or tips, producing human

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<v Speaker 1>chromosome two. Thus, humans have one fewer pair of chromosomes.

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<v Speaker 1>This is one of the main differences between the human

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<v Speaker 1>genome and the genome of our closest relatives. Now let's

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<v Speaker 1>get back to that sperm and egg issue. These cells

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<v Speaker 1>only have one homologous chromosome from each pair and are

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<v Speaker 1>therefore considered haploid. Here's why. When a sperm and egg fuse,

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<v Speaker 1>they combine their genetic material to form one complete diploid

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<v Speaker 1>set of chromosomes. And if you think about it, that

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<v Speaker 1>makes perfect sense. It means each parent contributes one set

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<v Speaker 1>to a pair of chromosomes in their child cells. Consider

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<v Speaker 1>blood type as a clear example. People with a B

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<v Speaker 1>blood type inherited two different gene variations on their two

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<v Speaker 1>homologous chromosomes, one for A and one for B that

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<v Speaker 1>when combined, produced a B Okay, So twenty three pairs

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<v Speaker 1>of chromosomes is typical for humans. But life doesn't always

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<v Speaker 1>go by the book. So what happens if something causes

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<v Speaker 1>more or fewer chromosomes to develop. A gain or loss

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<v Speaker 1>of chromosomes from these standard forty six is called an euploidy,

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<v Speaker 1>and it can occur either during the formation of reproductive

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<v Speaker 1>cells the sperm in the egg, or in early fetal development,

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<v Speaker 1>or in any other cell of the body after birth.

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<v Speaker 1>One of the most common forms of antiploidy is trisome,

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<v Speaker 1>which is the presence of an extra chromosome in the cells.

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<v Speaker 1>One well known result of trisome is Down syndrome, which

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<v Speaker 1>is a condition caused by three copies of chromosome twenty

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<v Speaker 1>one in each cell. This extra chromosome leads to a

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<v Speaker 1>total of forty seven chromosomes per cell rather than forty six.

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<v Speaker 1>The loss of one chromosome in a cell is called monosomey.

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<v Speaker 1>That's when people have just one copy of a specific

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<v Speaker 1>chromosome per cell as opposed to two. For example, Turner syndrome,

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<v Speaker 1>in which women have only one copy of the X

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<v Speaker 1>chromosome per cell versus the regular two, is a form

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<v Speaker 1>of monosomey. There are other variations of ante eploidy as well,

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<v Speaker 1>and in extreme cases, they may compromise a person's life. Additionally,

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<v Speaker 1>cancer cells also have alterations in their number of chromosomes.

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<v Speaker 1>Unlike the variations that happen in reproductive cells, these changes

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<v Speaker 1>cannot be inherited. Today's episode is based on the article

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<v Speaker 1>why do most humans have three pairs of chromosomes? On

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<v Speaker 1>how stuff works dot Com written by Michelle Konstantinovski. Brain

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<v Speaker 1>Stuff is production of I Heart Radio in partnership with

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<v Speaker 1>how stuff works dot Com and is produced by Tyler Clang.

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