Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Am J Hum Genet. 2010 May 14;86(5):674-85. doi: 10.1016/j.ajhg.2010.03.001. Epub 2010 Apr 8.
Coevolving interacting genes undergo complementary mutations to maintain their interaction. Distinct combinations of alleles in coevolving genes interact differently, conferring varying degrees of fitness. If this fitness differential is adequately large, the resulting selection for allele matching could maintain allelic association, even between physically unlinked loci. Allelic association is often observed in a population with the use of gametic linkage disequilibrium. However, because the coevolving genes are not necessarily in physical linkage, this is not an appropriate measure of coevolution-induced allelic association. Instead, we propose using both composite linkage disequilibrium (CLD) and a measure of association between genotypes, which we call genotype association (GA). Using a simple selective model, we simulated loci and calculated power for tests of CLD and GA, showing that the tests can detect the allelic association expected under realistic selective pressure. We apply CLD and GA tests to the polymorphic, physically unlinked, and putatively coevolving human gamete-recognition genes ZP3 and ZP3R. We observe unusual allelic association, not attributable to population structure, between ZP3 and ZP3R. This study shows that selection for allele matching can drive allelic association between unlinked loci in a contemporary human population, and that selection can be detected with the use of CLD and GA tests. The observation of this selection is surprising, but reasonable in the highly selected system of fertilization. If confirmed, this sort of selection provides an exception to the paradigm of chromosomal independent assortment.
共同进化的相互作用基因经历互补突变以维持其相互作用。共同进化基因中不同等位基因的独特组合以不同的方式相互作用,赋予不同程度的适合度。如果这种适合度差异足够大,那么等位基因匹配的选择就可以维持等位基因的关联,即使在物理上不相关的基因座之间也是如此。等位基因关联在使用配子连锁不平衡的群体中经常观察到。然而,由于共同进化的基因不一定在物理连锁上,因此这不是衡量共同进化诱导的等位基因关联的适当方法。相反,我们建议同时使用复合连锁不平衡 (CLD) 和基因型之间关联的度量,我们称之为基因型关联 (GA)。使用简单的选择模型,我们模拟了基因座,并计算了 CLD 和 GA 检验的功效,表明这些检验可以检测到在现实选择压力下预期的等位基因关联。我们将 CLD 和 GA 检验应用于多态性、物理上不相关且假定共同进化的人类配子识别基因 ZP3 和 ZP3R。我们观察到 ZP3 和 ZP3R 之间存在异常的等位基因关联,这归因于群体结构。这项研究表明,等位基因匹配的选择可以驱动当代人类群体中非连锁基因座之间的等位基因关联,并且可以使用 CLD 和 GA 检验来检测选择。观察到这种选择是令人惊讶的,但在受精这个高度选择的系统中是合理的。如果得到证实,这种选择将为染色体独立分配的范例提供一个例外。