Abstract
The development of molecular genetic markers, detecting variation at the DNA level, has opened new horizons in the genetic analyses of both man and agricultural species. Agricultural applications of “Restriction Fragment Length Polymorphisms” (RFLPs), despite their promise, are limited by the formidable costs involved in examining the large populations required. It is the purpose of this contribution to point out that the introduction of oligonucleotide probes into agricultural genetics may provide a solution to the cost problems. Furthermore, the number of detectable “Oligonucleotide Polymorphisms” (OPs) should exceed by an order of magnitude the number amenable to RFLP techniques, thus opening the gates to additional applications.
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In this procedure DNA is digested by restriction enzymes, the fragments generated are separated by size on a gel, transferred to a solid support, and hybridized to a labeled cloned sequence acting as probe (see ref. 15). Point mutations or small structural changes (e. g. deletions, additions, inversions) in the vicinity of the genomic DNA regions homologous to the probe will affect the length of the fragment containing the probe-homologous sequence. This can be detected as a change—termed an RFLP—in the location of the hybridization band on autoradiography.
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Beckmann, J. Oligonucleotide Polymorphisms: A New Tool for Genomic Genetics. Nat Biotechnol 6, 1061–1064 (1988). https://doi.org/10.1038/nbt0988-1061
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DOI: https://doi.org/10.1038/nbt0988-1061
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