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Estimating Y Chromosome Specific Microsatellite Mutation Frequencies using Deep Rooting Pedigrees

Évelyne HeyerLaboratoire D'Athropologie Biologique CNRS UMR152, Musee de L'Homme, Paris, FranceJack PuymiratUnité de recherche en Génétique Humaine, CHU Laval, 2705 boulevard Laurier, Ste-Foy, Quebec, G1V 4G2, CanadaPatrick DieltjesMGC-Department of Human Genetics, Leiden University, P.O. Box 9503, 2300 RA Leiden, The NetherlandsEgbert BakkerMGC-Department of Human Genetics, Leiden University, P.O. Box 9503, 2300 RA Leiden, The NetherlandsPeter de KnijffMGC-Department of Human Genetics, Leiden University, P.O. Box 9503, 2300 RA Leiden, The Netherlands
1997en
ABI

Abstract

Recently, a set of highly polymorphic chromosome Y specific microsatellites became available for forensic, population genetic and evolutionary studies. However, the lack of a mutation frequency estimate for these loci prevents a reliable application. We therefore used seven chromosome Y tetranucleotide repeat loci to screen 42 males who are descendants from 12 'founding fathers' by a total number of 213 generations. As a result, we were able to estimate an average chromosome Y tetranucleotide mutation frequency of 0.20% (95% CIL 0.05-0.55). This closely matches the often cited Weber and Wong estimate of 0.21% for a set of autosomal tetranucleotide repeats. Expanding the set of microsatellites with two more loci (a tri- and a penta-nucleotide repeat locus) an average chromosome Y microsatellite mutation frequency of 0.21% (95% CIL 0.06-0.49) was found. These estimates suggest that microsatellites on the Y chromosome have mutation frequencies comparable to those on the autosomes. This supports the hypothesis that slippage-generated growth is the driving force behind the microsatellite variability.

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