Molecular Biology and Evolution, Vol 11, 120-127, Copyright © 1994 by Society for Molecular Biology and Evolution
L Jin and R Chakraborty
DNA fingerprinting exhibits multilocus genotypes of individuals, detected
by the use of a single multilocus probe. Consequently, population data on
DNA fingerprinting do not provide a complete characterization of the
genetic variation in terms of allele-frequency distributions, since neither
the number of loci nor the locus affiliation of alleles is directly
observable. Yet DNA fingerprinting has been proved to be a cost-effective
method of detecting hypervariable polymorphisms in several organisms, where
the traditional loci fail to detect enough variation for microevolutionary
studies. In the present paper we demonstrate that the above-mentioned
features of DNA fingerprinting data do not cause any serious problem when
they are used in evolutionary studies. Bias-corrected estimators of Nei's
standard and minimum genetic distances are derived, and, by an application
of this theory to data on seven short tandem repeat loci in three major
human populations, it is shown that these modified measures of genetic
distances based on DNA fingerprint patterns are quite close to Nei's
distances based on locus-specific allele frequencies. Empirical as well as
theoretical support of the adequacy of such genetic distances from DNA
fingerprinting data is also discussed, and it indicates that the technical
limitations of DNA fingerprinting should not deter the use of the method
for short-term evolutionary studies.
ORIGINAL ARTICLE
Estimation of genetic distance and coefficient of gene diversity from single-probe multilocus DNA fingerprinting data
Center for Demographic and Population Genetics, University of Texas Houston Health Science Center.
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