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RAPD Markers Using PCR for Mapping and Crop Improvement - The technique of polymerase chain reaction (PCR), which has revolutionized a variety of techniques used in molecular biology, was earlier described in Chapter 4. As discussed there, original PCR technique has been variously modified to suit a range of needs.
One such variation produces 'Randomly Amplified Polymorphic DNAs (RAPDs)'. The use of RAPDs in preparation of linkage maps. The procedure is simple, quick to perform, requires relatively very small amounts of DNA and involves no radioactivity.
A comparison of the properties of RFLPs and RAPDs is presented. In early 1990's it was also shown that for RAPDs,. instead of using a pair of oligonucleotides as primers, a single short oligonucleotide primer can be successfully used.

This is based on the probability that a given DNA sequence (complementary to that of the primer) will occur in the genome, on opposite DNA strands, in opposite orientation, within a reasonable distance amplifiable by PCR.

For most plant materials, primers that are 9-10 nucleotides long (random sequences with at least 50% G and C and lacking inverted repeats) are predicted to generate, on an average, 2-10 amplification products. Polymorphism results mainly due to changes in the primer binding site's presence or absence, and amplification products represent one allele per locus.

The use of PCR technology for preparation of genetic maps and for a variety of crop improvement programmes will be discussed in this section.