The Ploymerase chain reaction (PCR)

The polymerase chain reaction (PCR) provides a simple and ingenious method for exponentially amplification of specific DNA sequences by in vitro DNA synthesis. This technique was developed by Kary Mullis at Cetus Corporation in Emery Ville, California in 1985. Kary Mullis shared the Nobel prize for chemistry in 1993. This technique has made it possible to synthesis large quantities of a DNA fragment without cloning it. It is ideally suited where the quantity of biological specimen available is very low such as a single hair strand or a tiny blood stain left at the site of a crime. The details of PCR techniques and its mechanism are described by Erlich (1989) in his edited book 'PCT Technology'. The PCR technique has now been automated and is carried out by a specially designed machine.

The working system of PCR.

Amplification of DNA:
The PCR includes the following three essential steps to amplify a specific DNA sequence.

i) Melting of target DNA: The target DNA containing sequence (between 100 and 5,000 base) to be amplified is heat denatured (around 94 Degree C for 15 second) to separate its complementary strands (step 1). This process is called melting of target DNA.

ii) Annealing of primers: The second step is the annealing of two oligonucleotide primers to the denatured DNA strands. Primers are added in excess and the temperature lowered to about 68 Degree C for 60 seconds consequently the primers form hydrogen bonds i.e. anneal to the DNA on both sides of the DNA sequence (step 2).

iii) Primer extension: Finally, nucleoside triphosphate (dATP, dGTP, dCTP, dTTP) and a thermostable DNA polymerase are added to the reaction mixture. The DNA polymerase is added to the reaction mixture. The DNA polymerase accelerates the polymerization process of primers and, therefore, extends the primers (at 68 Degree C) resulting in synthesis of copies of target DNA sequence (step 3). Only those DNA polymerases which are thermostable i.e. function at the high temperature are employed in PCT technique. For this purpose the two popular enzymes, Taq polymerase (of a thermophilic bacterium, Thermus aquaticus) and the vent polymerase (from Thermococcus litoralis) are used in PCR technology. These enzymes exhibit relative stability at DNA-melting replenishment after each cycle of synthesis. Also it reduces the cost of PCR and allows automated thermal cycling.

However, after completion of step 3 (of one cycle) the targeted sequences on both strands are copied and four strands are produced. Now, the three step cycle (first cycle) is repeated which yields 8 copies from four strands.

Similarly, the third cycle produces 16 strands. This cycle is repeated about 50 times. Theoretically, 20 cycles (each of three steps) will produce about one million copies of the target DNA sequence, and 30 cycles will produce about one billion copies. In each cycle the newly synthesized DNA strands serve as targets for subsequent DNA synthesis as the three steps are repeated up to 50 times. For the working of PCR about 10-100 picomoles of primers are required the concentration of target DNA can be about 10-20 to 10-15 M (or 1 to 105 DNA copies per ml). The PCR machine can carry out 25 cycles and amplify DNA 100000 times in 75 minutes.

The PCT technology has been improved in recent years. RNA can also be efficiently used in PCR technology. The rTth DNA polymerase is used instead of the Taq polymerase. The rTth polymerase will transcribe RNA to DNA, therefore amplify the DNA. Therefore, cellular RNA and RNA viruses may be studied when they are present in small quantities.