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A Simple Genetic Incompatibility Causes Hybrid Male Sterility in Mimulus

机译:一个简单的遗传不相容性导致杂种雄性不育

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摘要

Much evidence has shown that postzygotic reproductive isolation (hybrid inviability or sterility) evolves by the accumulation of interlocus incompatibilities between diverging populations. Although in theory only a single pair of incompatible loci is needed to isolate species, empirical work in Drosophila has revealed that hybrid fertility problems often are highly polygenic and complex. In this article we investigate the genetic basis of hybrid sterility between two closely related species of monkeyflower, Mimulus guttatus and M. nasutus. In striking contrast to Drosophila systems, we demonstrate that nearly complete hybrid male sterility in Mimulus results from a simple genetic incompatibility between a single pair of heterospecific loci. We have genetically mapped this sterility effect: the M. guttatus allele at the hybrid male sterility 1 (hms1) locus acts dominantly in combination with recessive M. nasutus alleles at the hybrid male sterility 2 (hms2) locus to cause nearly complete hybrid male sterility. In a preliminary screen to find additional small-effect male sterility factors, we identified one additional locus that also contributes to some of the variation in hybrid male fertility. Interestingly, hms1 and hms2 also cause a significant reduction in hybrid female fertility, suggesting that sex-specific hybrid defects might share a common genetic basis. This possibility is supported by our discovery that recombination is reduced dramatically in a cross involving a parent with the hms1–hms2 incompatibility.
机译:许多证据表明,合子后生殖隔离(杂种不育或不育)是由于不同种群之间的节间不相容性积累而形成的。尽管理论上只需要一对不兼容的基因座即可分离物种,但果蝇的实证研究表明杂种育性问题通常是高度多基因的和复杂的。在本文中,我们研究了两个密切相关的猴花杂交种(不育种guttatus和Na.tus Nasutus)的遗传基础。与果蝇系统形成鲜明对比的是,我们证明了mul鼠中几乎完全杂交的雄性不育是由一对异源基因座之间的简单遗传不相容引起的。我们对这种不育作用进行了遗传定位:杂种雄性不育1(hms1)基因座上的gu.tus等位基因与杂种雄性不育2(hms2)基因座上的隐性纳苏氏等位基因共同起作用,导致几乎完全杂种雄性不育。在初步筛选中,发现了其他影响较小的雄性不育因素,我们确定了一个另外的基因座,其也有助于杂种雄性不育的某些变异。有趣的是,hms1和hms2也会导致杂交女性的生育力显着降低,这表明性别特异性的杂交缺陷可能具有共同的遗传基础。我们的发现支持这种可能性,即在涉及具有hms1–hms2不相容性的亲本的杂交中,重组显着降低。

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