Final answer:
Primers are specific DNA sequences that mark the start and end of the region to be amplified during PCR. They bind to complementary sequences in the DNA template and are then extended by a polymerase enzyme, resulting in the desired PCR product after multiple cycles of amplification.
Step-by-step explanation:
The area where primers bind indeed dictates where the PCR product will be synthesized. Primers are short DNA fragments that are chemically synthesized to be complementary to specific sequences at the 3'-ends of the DNA template strands. By binding to these specific sites, primers act as starting points for DNA polymerization during PCR amplification. During PCR, the double-stranded DNA template is first denatured by heating to 94°C to separate the strands. Upon cooling to 55°C, primers anneal to the complementary sequences on the template strands, marking the beginning and end of the region to be amplified. The DNA polymerase enzyme then extends the primers, creating new strands of DNA that mirror the original template.
In the subsequent cycles of PCR, these newly synthesized DNA segments serve as additional templates, leading to an exponential increase in the number of copies of the specific target DNA region. The primers' specificity is crucial for determining the exact DNA segment that will be amplified. This specificity allows for the targeted amplification of a particular gene or DNA fragment, even within complex mixtures or genomic DNA.
By the second cycle of PCR, the primers preferentially anneal to the amplified DNA over the original template due to the increased concentration of the amplified DNA. Thus, the process results in the desired synthesized product, and any non-specifically amplified sequences from the first cycle are outcompeted by the specific product.