Estimating Y chromosome specific microsatellite mutation frequencies using deep rooting pedigrees

被引:214
作者
Heyer, E
Puymirat, J
Dieltjes, P
Bakker, E
deKnijff, P
机构
[1] LEIDEN UNIV,DEPT HUMAN GENET,MGC,NL-2300 RA LEIDEN,NETHERLANDS
[2] MUSEE HOMME PARIS,LAB ATHROPOL BIOL,CNRS,UMR 152,F-75116 PARIS,FRANCE
[3] CHU LAVAL,UNITE RECH GENET HUMAINE,ST FOY,PQ G1V 4G2,CANADA
关键词
D O I
10.1093/hmg/6.5.799
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 pentanucleotide 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.
引用
收藏
页码:799 / 803
页数:5
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