Polymerase chain reaction, or PCR, uses repeated cycles of heating and
cooling to make many copies of a specific region of DNA. First, the
temperature is raised to near boiling, causing the double-stranded DNA
to separate, or denature, into single strands. When the temperature is
decreased, short DNA sequences known as primers bind, or anneal, to
complementary matches on the target DNA sequence. The primers bracket
the target sequence to be copied. At a slightly higher temperature, the
enzyme Taq polymerase, shown here in blue, binds to the primed sequences
and adds nucleotides to extend the second strand. This completes the
first cycle. In subsequent cycles, the process of denaturing, annealing
and extending are repeated to make additional DNA copies. After three
cycles, the target sequence defined by the primers begins to accumulate.
After 30 cycles, as many as a billion copies of the target sequence are
produced from a single starting molecule.
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