Kimura M
National Institute of Genetics, Mishima 411, Japan.
Proc Natl Acad Sci U S A. 1980 Jan;77(1):522-6. doi: 10.1073/pnas.77.1.522.
We consider a single locus, and denote by A the wild-type allele and by A' the mutant allele that is produced irreversibly in each generation from A at the rate v. Let 1 + s, 1 + h, and 1 be, respectively, the relative fitnesses of mutant homozygote A'A', mutant heterozygote A'A, and wild-type homozygote AA. Then, it is shown, on the basis of the diffusion equation method, that the average time until fixation of the mutant allele (A') in a randomly mating population of effective size N(e), given that the initial frequency is p, is [Formula: see text] in which B(x) = (S/2)x(2) + Hx(1 - x), S = 4N(e)s, H = 4N(e)h, and V = 4N(e)v. Of particular interest are the cases in which the mutant allele is deleterious (s = -s', s' > 0). Three cases are considered; the mutant is: (i) completely dominant s = h = -s', (ii) completely recessive s = -s', h = 0, and (iii) semidominant s = -s', h = -s'/2, in which s' is the selection coefficient against the mutant homozygote. It is shown that the average time until fixation is shorter when the deleterious mutant allele is dominant than when it is recessive if 4N(e)v is larger than 1. On the other hand, the situation is reversed if 4N(e)v is smaller than 1. It is also shown that for a mutant allele for which N(e)s' > 10, it takes such a long time until fixation that we can practically ignore the occurrence of random fixation of a deleterious allele under continued mutation pressure. To supplement the analytical treatment, extensive simulation experiments were performed by using a device called the pseudo-sampling variable, which can enormously accelerate the process of simulation by a computer. This method simulates the diffusion process itself rather than the binominal sampling process (in population genetics the diffusion model is usually regarded as an approximation of the discrete binomial sampling process).
我们考虑一个单基因座,用(A)表示野生型等位基因,用(A')表示在每一代中以速率(v)由(A)不可逆产生的突变等位基因。设(1 + s)、(1 + h)和(1)分别为突变纯合子(A'A')、突变杂合子(A'A)和野生型纯合子(AA)的相对适合度。然后,基于扩散方程方法表明,在有效大小为(N(e))的随机交配群体中,给定初始频率为(p)时,突变等位基因((A'))固定的平均时间为[公式:见文本],其中(B(x) = (S/2)x(2) + Hx(1 - x)),(S = 4N(e)s),(H = 4N(e)h),(V = 4N(e)v)。特别令人感兴趣的是突变等位基因有害的情况((s = -s'),(s' > 0))。考虑了三种情况;突变体为:(i)完全显性(s = h = -s'),(ii)完全隐性(s = -s'),(h = 0),以及(iii)半显性(s = -s'),(h = -s'/2),其中(s')是针对突变纯合子的选择系数。结果表明,如果(4N(e)v)大于(1),有害突变等位基因显性时固定的平均时间比隐性时短。另一方面,如果(4N(e)v)小于(1),情况则相反。还表明,对于(N(e)s' > 10)的突变等位基因,直到固定需要很长时间,以至于在持续突变压力下,我们实际上可以忽略有害等位基因随机固定的发生。为了补充分析处理,使用一种称为伪采样变量的装置进行了广泛的模拟实验,该装置可以极大地加速计算机模拟过程。此方法模拟扩散过程本身,而不是二项采样过程(在群体遗传学中,扩散模型通常被视为离散二项采样过程的近似)。