Abstract

Hypervariabal minisatellite DNA is a recently described class of nuclear sequences with no known biological function. The minisatellites do form a subtype of restricition fragment length polymorphisms possessing several characteristics particularly intriguing to anthropologists interested in forensics, sociobiology, primate conservation, genetic variability, and molecular evolution. The sequence occupy at least five dozen loci scattered throughout the human genome. Unlike many polymorphisms, many of the loci have numerous alleles each present at similar frequencies. Such a genetic structure produces exceptionally high levels of heterozygosity and thus provides a tool for the individualization of tissue samples. Additionally, as the alleles are inherited in a Mendelian fashion, the minisatellites provide a superb tool for the identification of paternity (or maternity). Unlike standard blood groups, levels of variability are so high in populations studied to data that parentage can be established by inclusion rather than exclution. Homologous sequences are shown to exist in a variety of Old World primates. Visualization of genetic fingerprints in nonhumans may allow for determination of paternity where the pool of potential sires is available, while also providing information on levels of genetic variability. These capabilities will ultimately provide for better management of primate colonies. Used in concert with behavioral data, a number of sociobiological will also become more amenable to investigation.

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