Department of Zoology, Faculty of Science, Charles University in Prague, Viničná 7, 128 43 Prague 2, Czech Republic.
Mol Ecol. 2012 Jun;21(12):3032-47. doi: 10.1111/j.1365-294X.2012.05583.x. Epub 2012 May 14.
Studies of a hybrid zone between two house mouse subspecies (Mus musculus musculus and M. m. domesticus) along with studies using laboratory crosses reveal a large role for the X chromosome and multiple autosomal regions in reproductive isolation as a consequence of disrupted epistasis in hybrids. One limitation of previous work has been that most of the identified genomic regions have been large. The goal here is to detect and characterize precise genomic regions underlying reproductive isolation. We surveyed 1401 markers evenly spaced across the genome in 679 mice collected from two different transects. Comparisons between transects provide a means for identifying common patterns that likely reflect intrinsic incompatibilities. We used a genomic cline approach to identify patterns that correspond to epistasis. From both transects, we identified contiguous regions on the X chromosome in which markers were inferred to be involved in epistatic interactions. We then searched for autosomal regions showing the same patterns and found they constitute about 5% of autosomal markers. We discovered substantial overlap between these candidate regions underlying reproductive isolation and QTL for hybrid sterility identified in laboratory crosses. Analysis of gene content in these regions suggests a key role for several mechanisms, including the regulation of transcription, sexual conflict and sexual selection operating at both the postmating prezygotic and postzygotic stages of reproductive isolation. Taken together, these results indicate that speciation in two recently diverged (c. 0.5 Ma) house mouse subspecies is complex, involving many genes dispersed throughout the genome and associated with distinct functions.
对两个家鼠亚种(Mus musculus musculus 和 M. m. domesticus)杂交区的研究以及使用实验室杂交的研究表明,X 染色体和多个常染色体区域在生殖隔离中起重要作用,这是由于杂种中错义的破坏。以前工作的一个限制是,大多数已确定的基因组区域都很大。这里的目标是检测和描述生殖隔离背后的精确基因组区域。我们在从两条不同截线收集的 679 只小鼠中调查了基因组上均匀分布的 1401 个标记。截线之间的比较提供了一种识别可能反映内在不兼容性的共同模式的方法。我们使用基因组渐变方法来识别与错义相关的模式。从两条截线中,我们确定了 X 染色体上的连续区域,推断这些区域中的标记涉及错义相互作用。然后,我们搜索显示相同模式的常染色体区域,发现它们构成了大约 5%的常染色体标记。我们发现生殖隔离和实验室杂交中鉴定的杂种不育 QTL 背后的这些候选区域之间存在大量重叠。对这些区域中的基因内容的分析表明,包括转录调控、性冲突和性选择在内的几种机制在生殖隔离的后配前合子和后合子阶段都起着关键作用。总的来说,这些结果表明,两个最近分化(约 0.5 Ma)的家鼠亚种的物种形成是复杂的,涉及到基因组中散布的许多基因,并与不同的功能相关。