DNA sequencing is used to determine the nucleotides in a DNA strand. A sequencing method called dideoxy sequencing (also known as chain termination method or Sanger method uses a primer as a start marker for the chain reaction. Hybridization probes are primers that carry one or more fluorescent chemicals. Their fluorescence changes when they bind to a matching DNA sequence. Hybridization probes are used for detecting the location or quantity of DNA, e.g., in a PCR reaction.
In Polymerase Chain Reaction, primers are used to determine the DNA fragment to be amplified by the PCR process. The length of primers is usually not more than 50 nucleotides (Since DNA is usually double-stranded, its length is measured in base pairs. The length of single-stranded DNA is measured in bases or nucleotides.), and they match exactly the beginning and the end of the DNA fragment to be amplified. They anneal (adhere) to the DNA template at these starting and ending points, where the DNA-Polymerase binds and begins the synthesis of the new DNA strand.
The choice of the length of the primers and their melting temperature depends on a number of considerations. The melting (or annealing) temperature of a primer is defined as the temperature below which the primer will anneal to the DNA template and above which the primer will dissociate (break apart) from the DNA template. The melting temperature required increases with the length of the primer. Primers that are too short would anneal at several positions on a long DNA template, which would result in non-specific copies. On the other hand, the length of a primer is limited by the temperature required to melt it. Melting temperatures that are too high, i.e., above 80°C, can also cause problems since the DNA-Polymerase is less active at such temperatures. The optimum length of a primer is generally from 30 to 40 nucleotides with a melting temperature between about 60°C and 75°C. There are several ways to calculate the melting temperature (TM) of primers. (A, G, C and T are the number of nucleotides in the primer, respectively. [Na+] is the concentration of Na+ in the PCR vial.)
Also, a primer should not easily anneal with itself or others of its kind, building loops or hairpins in the process. This could hinder the annealing with the template DNA. However, small hairpins are usually unavoidable.
A Primer is also a common name for any substance used to start a fire.
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