The genes you don't get from your parents (but can't live without) - Devin Shuman

2,089,731 views ・ 2021-10-05

TED-Ed


Please double-click on the English subtitles below to play the video.

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Inside our cells, each of us has a second set of genes
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completely separate from the 23 pairs of chromosomes
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we inherit from our parents.
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And this isn’t just the case for humans—
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it’s true of every animal, plant, and fungus,
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and nearly every multicellular organism on Earth.
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This second genome belongs to our mitochondria,
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an organelle inside our cells.
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They’re not fully a part of us, but they’re not separate either—
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so why are they so different from anything else in our bodies?
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Approximately 1.5 billion years ago,
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scientists think a single-celled organism engulfed the mitochondria’s ancestor,
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creating the predecessor of all multicellular organisms.
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Mitochondria play an essential role:
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they convert energy from the food we eat and oxygen we breathe
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into a form of energy our cells can use, which is a molecule called ATP.
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Without this energy, our cells start to die.
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Humans have over 200 types of cells,
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and all except mature red blood cells have mitochondria.
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That’s because a red blood cell’s job is to transport oxygen,
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which mitochondria would use up before it could reach its destination.
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So all mitochondria use oxygen and metabolites to create energy
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and have their own DNA,
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but mitochondrial DNA varies more across species than other DNA.
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In mammals, mitochondria usually have 37 genes.
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In some plants, like cucumbers, mitochondria have up to 65 genes,
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and some fungal mitochondria have only 1.
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A few microbes that live in oxygen-poor environments
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seem to be on the way to losing their mitochondria entirely,
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and one group, oxymonad monocercomonoides, already has.
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This variety exists because mitochondria are still evolving,
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both in tandem with the organisms that contain them,
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and separately, on their own timeline.
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To understand how that’s possible,
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it helps to take a closer look at what the mitochondria inside us are doing,
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starting from the moment we’re conceived.
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In almost all species, mitochondrial DNA is passed down from only one parent.
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In humans and most animals, that parent is the mother.
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Sperm contain approximately 50 to 75 mitochondria in the tail,
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to help them swim.
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These dissolve with the tail after conception.
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Meanwhile, an egg contains thousands of mitochondria,
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each containing multiple copies of the mitochondrial DNA.
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This translates to over 150,000 copies of mitochondrial DNA
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that we inherit from our mothers,
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each of which is independent and could vary slightly from the others.
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As a fertilized egg grows and divides,
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those thousands of mitochondria are divvied up into the cells
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of the developing embryo.
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By the time we have differentiated tissues and organs,
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variations in the mitochondrial DNA are scattered at random throughout our bodies.
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To make matters even more complex,
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mitochondria have a separate replication process from our cells.
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So as our cells replicate by dividing, mitochondria end up in new cells,
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and all the while they’re fusing and dividing themselves,
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on their own timeline.
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As mitochondria combine and separate,
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they sequester faulty DNA or mitochondria that aren’t working properly for removal.
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All this means that the random selection of your mother’s mitochondrial DNA
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you inherit at birth
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can change throughout your life and throughout your body.
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So mitochondria are dynamic and, to a degree, independent,
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but they’re also shaped by their environments: us.
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We think that long ago,
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some of their genes were transferred to their host’s genomes.
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So today, although mitochondria have their own genome
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and replicate separately from the cells that contain them,
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they can't do this without instruction from our DNA.
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And though mitochondrial DNA is inherited from one parent,
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the genes involved in building and regulating the mitochondria
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come from both.
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Mitochondria continue to defy tidy classification.
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Their story is still unfolding inside of each of our cells,
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simultaneously separate and inseparable from our own.
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Learning more about them can both give us tools
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to protect human health in the future, and teach us more about our history.
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