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History of PCR

Polymerase Chain Reaction (PCR)


A triumvirate of methods - Cloning, DNA sequencing, and PCR (Polymerase Chain
Reaction)- underlies almost all of modern molecular biology. Of these three, the PCR is the
oldest in theory and the most versatile in practice. The method was first proposed in the
early 1970s by H. Ghobind Khorana and his colleagues as a strategy to lessen the labor
involved in chemical synthesis of genes. Their ideas, however, did not seem practicable at
a time when genes had not yet been sequenced, thermostable DNA polymerases had not
been described, and synthesis of oligonucleotide primers was more of an art than a
science. Not surprisingly, Khorana's ideas were quickly forgotten. The technique was
independently conceived 15 years later, given its present name, and put into practice by
biochemist Kary Mullis and coworkers at Cetus Corporation, who described in vitro
amplification of single-copy mammalian genes using the Klenow fragment of Escherichia
coli DNA polymerase I. Even so, PCR would probably have remained a clumsy laboratory
curiosity were it not for the discovery of thermostable DNA polymerases. The use of a
thermostable polymerase from Thermus aquaticus (Taq-pol) greatly increased the
efficiency of PCR and opened the doors to automation of the method. By the end of the
1980s, cloning was no longer the only way to isolate genes: DNA sequencing had been
revolutionized and PCR had become a fundamental cornerstone of genetic and molecular
analyses. In 1993 K.Mullis was awarded the Nobel Prize in Chemistry.
Appendix III Things to think about when programming a thermocycler
PCR is an iterative process, consisting of three steps: denaturation of the template by
heat, annealing of the oligonucleotide primers to the single-stranded target sequence(s),
and extension of the annealed primers by a thermostable DNA polymerase.
Denaturation. Double-stranded DNA templates denature at a temperature that is
determined in part by their G+C content. The higher the proportion of G+C, the higher the
temperature required to separate the strands of template DNA. The longer the DNA
molecules, the greater the time required at the chosen denaturation temperature to
separate the two strands completely. If the temperature for denaturation is too low or if the
time is too short, only AT-rich regions of the template DNA will be denatured. When the
temperature is reduced later in the PCR cycle, the template DNA will reanneal into a fully
native condition.
In PCRs catalyzed by Taq DNA polymerase, denaturation is carried out at 94-95C, which
is the highest temperature that the enzyme can endure for 30 or more cycles without
sustaining excessive damage. In the first cycle of PCR, denaturation is sometimes carried
out for 5 minutes to increase the probability that long molecules of template DNA are fully
denatured. However this extended period of denaturation is not always necessary for
linear DNA molecules and may sometimes be deleterious. Denaturation for 45 seconds at
94-95C is recommended for routine amplification of linear DNA templates whose contents
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of G+C is 55% or less.


Higher temperatures may be required to denature template and/or target DNAs that are
rich in G+C (>55%). DNA polymerases isolated from Archaea are more heat-tolerant than
Taq and are therefore preferred for amplification of GC-rich DNAs.
Annealing of primers to template DNA. The temperature used for the annealing step
(Ta) is critical. If the annealing temperature is too high, the oligonucleotide primers anneal
poorly, if at all, to the template and the yield of amplified DNA is very low. If the annealing
temperature is too low, nonspecific annealing of primers may occur, resulting in the
amplification of unwanted segments of DNA. Annealing is usually carried out 3-5C lower
than the calculated melting temperature at which the oligonucleotide primers dissociate
from their templates. Many formulas exist to determine the theoretical melting temperature,
but none of them are accurate for oligonucleotide primers of all lengths and sequences. It
is best to optimize the annealing conditions by performing a series of trial PCRs at
temperatures ranging from 2C to 10C below the lower of the melting temperatures
calculated for the two oligonucleotide primers. Alternatively, the thermal cycler can be
programmed to use progressively lower annealing temperatures in consecutive pairs of
cycles ("touchdown" PCR). Instead of surveying a variety of annealing conditions in
separate PCRs, optimization is achieved by exposing a single PCR to a sequential series
of annealing temperatures in successive cycles of the reaction. For many investigators,
touchdown PCR bypasses the need to determine the optimum annealing temperature for
every pair of primers and is used to obtain acceptable yields of amplified products in
routine PCR.
Number of cycles. The number of cycles required for amplification depends on the
number of copies of template DNA present at the beginning of the reaction and the
efficiency of primer extension and amplification. Once established in the geometric phase,
the reaction proceeds until one of the components becomes limiting. At this point, the yield
of specific amplification products should be maximal, whereas nonspecific amplification
products should be barely detectable, if not at all. This is generally the case after - 30
cycles in PCRs containing ~105 copies of the target sequence and Taq DNA polymerase.
At least 25 cycles are required to achieve acceptable levels of amplification of single-copy
target sequences in mammalian DNA templates.
Assuming 100% efficiency, the amount of product DNA is doubles with each PCR cycle.
This exponential amplification of target DNA makes PCR a very useful technology in
forensic science.

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