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The DNA in just one of your cells
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gets damaged tens of thousands
of times per day.
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Multiply that by your body's
hundred trillion or so cells,
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and you've got a quintillion
DNA errors everyday.
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And because DNA provides the blueprint
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for the proteins
your cells need to function,
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damage causes serious problems,
such as cancer.
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The errors come in different forms.
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Sometimes nucleotides,
DNA's building blocks, get damaged,
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other times nucleotides
get matched up incorrectly,
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causing mutations,
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and nicks in one or both strands
can interfere with DNA replication,
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or even cause sections
of DNA to get mixed up.
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Fortunately, your cells have ways
of fixing most of these problems
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most of the time.
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These repair pathways
all rely on specialized enzymes.
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Different ones respond
to different types of damage.
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One common error is base mismatches.
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Each nucleotide contains a base,
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and during DNA replication,
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the enzyme DNA polymerase
is supposed to bring in the right partner
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to pair with every base
on each template strand.
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Adenine with thymine,
and guanine with cytosine.
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But about once every
hundred thousand additions,
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it makes a mistake.
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The enzyme catches
most of these right away,
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and cuts off a few nucleotides
and replaces them with the correct ones.
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And just in case it missed a few,
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a second set of proteins
comes behind it to check it.
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If they find a mismatch,
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they cut out the incorrect nucleotide
and replace it.
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This is called mismatch repair.
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Together, these two systems reduce
the number of base mismatch errors
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to about one in one billion.
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But DNA can get damaged
after replication, too.
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Lots of different molecules
can cause chemical changes to nucleotides.
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Some of these come
from environmental exposure,
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like certain compounds in tobacco smoke.
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But others are molecules that are found
in cells naturally,
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like hydrogen peroxide.
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Certain chemical changes are so common
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that they have specific enzymes assigned
to reverse the damage.
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But the cell also has more general
repair pathways.
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If just one base is damaged,
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it can usually be fixed by a process
called base excision repair.
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One enzyme snips out the damaged base,
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and other enzymes come in to trim around
the site and replace the nucleotides.
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UV light can cause damage
that's a little harder to fix.
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Sometimes, it causes two adjacent
nucleotides to stick together,
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distorting the DNA's double helix shape.
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Damage like this requires
a more complex process
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called nucleotide excision repair.
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A team of proteins removes a long strand
of 24 or so nucleotides,
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and replaces them with fresh ones.
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Very high frequency radiation,
like gamma rays and x-rays,
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cause a different kind of damage.
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They can actually sever one
or both strands of the DNA backbone.
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Double strand breaks
are the most dangerous.
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Even one can cause cell death.
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The two most common pathways
for repairing double strand breaks
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are called homologous recombination
and non-homologous end joining.
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Homologous recombination uses an undamaged
section of similar DNA as a template.
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Enzymes interlace the damaged
and undamgaed strands,
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get them to exchange sequences
in nucleotides,
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and finally fill in the missing gaps
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to end up with two complete
double-stranded segments.
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Non-homologous end joining,
on the other hand,
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doesn't rely on a template.
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Instead, a series of proteins
trims off a few nucleotides
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and then fuses the broken ends
back together.
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This process isn't as accurate.
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It can cause genes to get mixed up,
or moved around.
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But it's useful when
sister DNA isn't available.
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Of course, changes to DNA
aren't always bad.
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Beneficial mutations
can allow a species to evolve.
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But most of the time,
we want DNA to stay the same.
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Defects in DNA repair are associated
with premature aging
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and many kinds of cancer.
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So if you're looking for
a fountain of youth,
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it's already operating in your cells,
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billions and billions of times a day.