Christie Paul, Macnair Mark R
Department of Biological Sciences, University of Exeter, Hatherly Laboratories, Exeter, Devon, UK.
Evolution. 1987 May;41(3):571-578. doi: 10.1111/j.1558-5646.1987.tb05827.x.
Postmating reproductive isolating barriers are generally believed to arise as the chance by-product of genetic differentiation. The classical view is that these barriers normally involve differentiation at many loci, and therefore require long periods of allopatric isolation. The formal genetics of, and the distribution of genes responsible for, such barriers are known in very few cases. This paper examines the distribution of the genes responsible for two different postmating barriers in 18 populations of the yellow monkey flower, Mimulus guttatus. The genetic relatedness of the populations was measured by a morphometrical analysis. Widespread polymorphism was found for three of the four components of the two genetic systems responsible for the two barriers, with at least 13 populations possessing genes for one or both of the barriers. In one system (the C7/U8 system; Christie and Macnair, 1984), the distribution of the two component genes was correlated with the morphometrical similarity and geographical location of the populations. This pattern could be produced by a historical association or by an adaptive response. In the other system (the Cerig/C10 system; Macnair and Christie, 1983), the genes were more widely dispersed, and there was no obvious morphometrical or geographical association. Populations possessing the complementary factors causing partial reproductive isolation are not always widely separated geographically. These results indicate that the spread of postmating reproductive isolating genes through drift, selection, or hitchhiking could readily cause reproductive isolation to evolve in this species.>.
通常认为交配后生殖隔离屏障是作为遗传分化的偶然副产物出现的。经典观点认为,这些屏障通常涉及多个基因座的分化,因此需要长时间的异域隔离。在极少数情况下,人们才了解此类屏障的形式遗传学以及负责这些屏障的基因分布。本文研究了黄猴面花(Mimulus guttatus)18个种群中导致两种不同交配后屏障的基因分布情况。通过形态计量分析来测量种群的遗传相关性。在负责这两种屏障的两个遗传系统的四个组成部分中,有三个发现了广泛的多态性,至少有13个种群拥有一种或两种屏障的基因。在一个系统(C7/U8系统;克里斯蒂和麦克奈尔,1984年)中,两个组成基因的分布与种群的形态计量相似性和地理位置相关。这种模式可能是由历史关联或适应性反应产生的。在另一个系统(Cerig/C10系统;麦克奈尔和克里斯蒂,1983年)中,基因分布更为广泛,且没有明显的形态计量或地理关联。拥有导致部分生殖隔离的互补因子的种群在地理上并不总是相距甚远。这些结果表明,通过漂变、选择或搭便车,交配后生殖隔离基因的传播很容易导致该物种进化出生殖隔离。