Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 66, Issue 5, Pages 1580-1588Publisher
CELL PRESS
DOI: 10.1086/302905
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A number of applications of analysis of human Y-chromosome microsatellite loci to human evolution and forensic science require reliable estimates of the mutation rate and knowledge of the mutational mechanism. We therefore screened a total of 4,999 meioses from father/son pairs with confirmed paternity (probability greater than or equal to 99.9%) at 15 Y-chromosomal microsatellite loci and identified 14 mutations. The locus-specific mutation-rate estimates were 0-8.58 x 10(-3), and the average mutation rate estimates were 3.17 x 10(-3) (95% confidence interval [CI] 1.89-4.94 x 10(-3)) across 8 tetranucleotide microsatellites and 2.80 x 10(-3) (95% CI 1.72-4.27 x 10(-3)) across all 15 Y-chromosomal microsatellites studied. Our data show a mutational bias toward length increase, on the basis of observation of more repeat gains than losses (10:4). The data are in almost complete agreement with the stepwise-mutation model, with 13 single-repeat changes and 1 double-repeat change. Sequence analysis revealed that all mutations occurred in uninterrupted homogenous arrays of greater than or equal to 11 repeats. We conclude that mutation rates and characteristics of human Y-chromosomal microsatellites are consistent with those of autosomal microsatellites. This indicates that the general mutational mechanism of microsatellites is independent of recombination.
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