Novel mutation processes in the evolution of a haploid minisatellite, MSY1: array homogenization without homogenization

被引:23
作者
Bouzekri, N
Taylor, PG
Hammer, MF
Jobling, MA
机构
[1] Univ Leicester, Dept Genet, Leicester LE1 7RH, Leics, England
[2] CHU Purpan, CNRS, UPR 8291, Ctr Immunopathol & Genet Humaine, F-31300 Toulouse, France
[3] Univ Arizona, Lab Mol Systemat & Evolut, Tucson, AZ 85721 USA
基金
英国惠康基金;
关键词
D O I
10.1093/hmg/7.4.655
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
The Y-specific locus MSY1 is the only known haploid minisatellite, and displays an extremely high degree of structural diversity which can be assayed by minisatellite variant repeat PCR (MVR-PCR). One group of alleles, in an African-specific class of Y chromosomes (haplogroup 8), behaves unusually in the conventional MVR-PCR assay, and sequencing demonstrates that this is because repeat units in these alleles contain an additional base substitution, We have designed a new MVR-PCR system to detect these novel variants, and show firstly that they are confined to the haplogroup 8 chromosomes, and secondly that the base substitution has spread through these arrays without the elimination of existing repeat variants, The sharing of a particular base substitution between otherwise distinct repeat types in these alleles represents evidence of a remarkable mutation process in their evolutionary history, in which the variant base must have been spread by a biased repair mechanism operating in very small patches within heteroduplexes.
引用
收藏
页码:655 / 659
页数:5
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