Nei M, Maruyama T, Wu C I
Genetics. 1983 Mar;103(3):557-79. doi: 10.1093/genetics/103.3.557.
Mathematical models are presented for the evolution of postmating and premating reproductive isolation. In the case of postmating isolation it is assumed that hybrid sterility or inviability is caused by incompatibility of alleles at one or two loci, and evolution of reproductive isolation occurs by random fixation of different incompatibility alleles in different populations. Mutations are assumed to occur following either the stepwise mutation model or the infinite-allele model. Computer simulations by using Itô's stochastic differential equations have shown that in the model used the reproductive isolation mechanism evolves faster in small populations than in large populations when the mutation rate remains the same. In populations of a given size it evolves faster when the number of loci involved is large than when this is small. In general, however, evolution of isolation mechanisms is a very slow process, and it would take thousands to millions of generations if the mutation rate is of the order of 10(-5) per generation. Since gene substitution occurs as a stochastic process, the time required for the establishment of reproductive isolation has a large variance. Although the average time of evolution of isolation mechanisms is very long, substitution of incompatibility genes in a population occurs rather quickly once it starts. The intrapopulational fertility or viability is always very high. In the model of premating isolation it is assumed that mating preference or compatibility is determined by male- and female-limited characters, each of which is controlled by a single locus with multiple alleles, and mating occurs only when the male and female characters are compatible with each other. Computer simulations have shown that the dynamics of evolution of premating isolation mechanism is very similar to that of postmating isolation mechanism, and the mean and variance of the time required for establishment of premating isolation are very large. Theoretical predictions obtained from the present study about the speed of evolution of reproductive isolation are consistent with empirical data available from vertebrate organisms.
本文提出了关于交配后和交配前生殖隔离进化的数学模型。在交配后隔离的情况下,假设杂种不育或不存活是由一个或两个基因座上等位基因的不相容性引起的,并且生殖隔离的进化是通过不同种群中不同不相容等位基因的随机固定而发生的。假设突变遵循逐步突变模型或无限等位基因模型。使用伊藤随机微分方程进行的计算机模拟表明,在所使用的模型中,当突变率保持不变时,生殖隔离机制在小种群中比在大种群中进化得更快。在给定大小的种群中,当涉及的基因座数量较多时,它比数量较少时进化得更快。然而,一般来说,隔离机制的进化是一个非常缓慢的过程,如果突变率为每代10^(-5) 左右,那么需要数千到数百万代。由于基因替代是一个随机过程,建立生殖隔离所需的时间有很大的方差。虽然隔离机制进化的平均时间非常长,但一旦开始,种群中不相容基因的替代发生得相当快。种群内的育性或活力总是非常高。在交配前隔离模型中,假设交配偏好或相容性由雄性和雌性受限性状决定,每个性状由具有多个等位基因的单个基因座控制,并且只有当雄性和雌性性状相互兼容时才会发生交配。计算机模拟表明,交配前隔离机制的进化动态与交配后隔离机制的非常相似,并且建立交配前隔离所需时间的均值和方差都非常大。从本研究中获得的关于生殖隔离进化速度的理论预测与脊椎动物的现有经验数据一致。