He Qun, Cederberg Håkan, Rannug Ulf
Department of Genetic and Cellular Toxicology, Stockholm University, S-106 91 Stockholm, Sweden.
J Mol Biol. 2002 May 31;319(2):315-27. doi: 10.1016/S0022-2836(02)00292-9.
Certain minisatellites exhibit hypervariability with respect to the number of repeat units and, thus, allele length. Such polymorphism is generated by germline-specific recombinational events that occur at high frequencies and lead to the gain or loss of repeat units. In order to elucidate the molecular details of mutagenesis in minisatellites, we have integrated human minisatellites into the yeast genome in the vicinity of a hotspot for meiotic double-strand breaks (DSBs). Here, we describe the results of tetrad analyses of mutations in the human MS205 minisatellite in yeast strains heterozygous for alleles composed of 51 and 31 repeat units, as well as in a strain homozygous for the same 51 repeat unit allele. The length-mutation rate was twice as high in the heterozygous strain as in the homozygous strain, suggesting that sequence divergence between alleles enhances the generation of length mutations. In the case of heterozygotes, the frequency of length mutants resulting from inter-allelic exchange was significantly higher in tetrads with three viable spores than in tetrads with four viable spores, indicating that there is a higher probability for spore mortality in tetrads originating from meioses during which inter-allelic exchange of repeat units occurs. In an attempt to explain these findings, we propose a model for minisatellite mutation involving recombination, in which sequence divergence between alleles results in a heteroduplex containing numerous mismatches. We suggest that convergent mismatch-repair tracts in this heteroduplex give rise to a DSB that may be repaired by an additional round of recombination resulting in mutation of a third allele, or be lethal if such recombination fails. It appears probable that the formation of such additional mutants is the major explanation for the difference in meiotic length-mutation rates between the heterozygous and homozygous yeast strains, and that this phenomenon contributes to high germline length-mutation frequencies at minisatellites in humans.
某些微卫星在重复单元数量以及等位基因长度方面表现出高度变异性。这种多态性是由种系特异性重组事件产生的,这些事件发生频率很高,并导致重复单元的增加或减少。为了阐明微卫星中诱变的分子细节,我们已将人类微卫星整合到酵母基因组中减数分裂双链断裂(DSB)热点附近。在这里,我们描述了对酵母菌株中人类MS205微卫星突变的四分体分析结果,这些酵母菌株对于由51个和31个重复单元组成的等位基因是杂合的,以及对于相同的51个重复单元等位基因是纯合的。杂合菌株中的长度突变率是纯合菌株中的两倍,这表明等位基因之间的序列差异会增强长度突变的产生。在杂合子的情况下,具有三个存活孢子的四分体中等位基因间交换产生的长度突变体频率明显高于具有四个存活孢子的四分体,这表明在发生重复单元等位基因间交换的减数分裂产生的四分体中,孢子死亡的可能性更高。为了解释这些发现,我们提出了一个涉及重组的微卫星突变模型,其中等位基因之间的序列差异导致含有大量错配的异源双链体。我们认为,这个异源双链体中收敛的错配修复片段会产生一个DSB,它可能通过额外一轮的重组进行修复,从而导致第三个等位基因突变,或者如果这种重组失败则是致死的。很可能这种额外突变体的形成是杂合和纯合酵母菌株减数分裂长度突变率差异的主要解释,并且这种现象导致了人类微卫星处种系长度突变频率较高。