Max-Planck Institut für Evolutionsbiologie, Abteilung Evolutionsgenetik, Plön, Germany.
Mol Biol Evol. 2010 Aug;27(8):1845-56. doi: 10.1093/molbev/msq064. Epub 2010 Mar 3.
Copy number variation (CNV) contributes significantly to natural genetic variation within and between populations. However, the mutational mechanisms leading to CNV, as well as the processes that control the size of CNV regions, are so far not well understood. Here, we have analyzed a gene family that forms CNV regions on the X and the Y chromosomes in Mus musculus. These CNV regions show copy number differences in two subspecies, M. musculus domesticus and M. musculus musculus. Assessment of copy numbers at these loci for individuals caught in a natural hybrid zone showed copy number increases and a large variance among individuals. Crosses of natural hybrid animals among each other produced even more extreme variants with major differences in copy number in the offspring from the same parents. To assess the inheritance pattern of the loci further, we have produced F1 and backcross hybrid animals from these subspecies. We found that copy number expansions can already be traced in F1 offspring and they became stronger in the backcross individuals. Specific analysis of hybrid male offspring indicated that neither meiotic recombination nor interchromosomal exchange was required for creating these changes because the X and Y chromosomes have no homologues in males. This suggests that intrachromosomal exchanges can drive CNV and that this can occur at an elevated frequency in interspecific crosses, even within an individual. Accordingly, we find copy number mosaicism in individuals, that is, DNA from different tissues of the same individual can have different copy numbers for the loci studied. A preliminary survey of autosomal loci suggests that these can also be subject to change in hybrids. Hence, we conclude that the effects we see are not only restricted to some specific loci but may also be caused by a general induction of replication-coupled repair processes.
拷贝数变异 (CNV) 在种群内和种群间对自然遗传变异有重要贡献。然而,导致 CNV 的突变机制以及控制 CNV 区域大小的过程到目前为止还不是很清楚。在这里,我们分析了一个在 X 和 Y 染色体上形成 CNV 区域的基因家族在 Mus musculus 中。这些 CNV 区域在两个亚种 M. musculus domesticus 和 M. musculus musculus 中显示出拷贝数差异。对在自然杂交区捕获的个体在这些基因座上的拷贝数进行评估显示,个体之间的拷贝数增加,个体之间的差异很大。自然杂交动物之间的杂交产生了更多的极端变体,其后代的拷贝数差异很大。为了进一步评估这些基因座的遗传模式,我们从这些亚种中产生了 F1 和回交杂交动物。我们发现,F1 后代中已经可以追踪到拷贝数扩展,并且在回交个体中变得更强。对杂种雄性后代的具体分析表明,减数分裂重组或染色体间交换不是产生这些变化所必需的,因为 X 和 Y 染色体在雄性中没有同源物。这表明染色体内交换可以驱动 CNV,并且这种情况在种间杂交中甚至在个体内都可以以更高的频率发生。因此,我们在个体中发现了拷贝数镶嵌现象,即同一个体的不同组织的 DNA 可以具有研究基因座的不同拷贝数。对常染色体基因座的初步调查表明,这些基因座也可能在杂种中发生变化。因此,我们得出结论,我们看到的影响不仅限于一些特定的基因座,也可能是由复制偶联修复过程的普遍诱导引起的。