Lessard Sabin, Rocheleau Ghislain
Département de mathématiques et de statistique, Université de Montréal, C.P. 6128, Succursale Centre-ville, Montréal, Qué., Canada H3C 3J7.
Theor Popul Biol. 2004 Dec;66(4):287-306. doi: 10.1016/j.tpb.2004.05.004.
We consider family specific fitnesses that depend on mixed strategies of two basic phenotypes or behaviours. Pairwise interactions are assumed, but they are restricted to occur between sibs. To study the change in frequency of a rare mutant allele, we consider two different forms of weak selection, one applied through small differences in genotypic values determining individual mixed strategies, the other through small differences in viabilities according to the behaviours chosen by interacting sibs. Under these two specific forms of weak selection, we deduce conditions for initial increase in frequency of a rare mutant allele for autosomal genes in the partial selfing model as well as autosomal and sex-linked genes in the partial sib-mating model with selection before mating or selection after mating. With small differences in mixed strategies, we show that conditions for protection of a mutant allele are tantamount to conditions for initial increase in frequency obtained in additive kin selection models. With particular reference to altruism versus selfishness, we provide explicit ranges of values for the selfing or sib-mating rate based on a fixed cost-benefit ratio and the dominance scheme that allow the spreading of a rare mutant allele into the population. This study confirms that more inbreeding does not necessarily promote the evolution of altruism. Under the hypothesis of small differences in viabilities, the situation is much more intricate unless an additive model is assumed. In general however, conditions for initial increase in frequency of a mutant allele can be obtained in terms of fitness effects that depend on the genotypes of interacting individuals or their mates and generalized conditional coefficients of relatedness according to the inbreeding condition of the interacting individuals.
我们考虑了特定于家庭的适合度,其取决于两种基本表型或行为的混合策略。假设存在成对相互作用,但仅限于同胞之间发生。为了研究稀有突变等位基因频率的变化,我们考虑两种不同形式的弱选择,一种是通过决定个体混合策略的基因型值的微小差异来应用,另一种是通过根据相互作用的同胞所选择的行为在生存能力上的微小差异来应用。在这两种特定形式的弱选择下,我们推导了部分自交模型中常染色体基因以及部分同胞交配模型中常染色体和性连锁基因在交配前选择或交配后选择时稀有突变等位基因频率初始增加的条件。通过混合策略的微小差异,我们表明保护突变等位基因的条件等同于在加性亲缘选择模型中获得的频率初始增加的条件。特别提及利他主义与自私,我们基于固定的成本效益比和显性模式提供了自交或同胞交配率的明确值范围,这些范围允许稀有突变等位基因在种群中传播。这项研究证实,更多的近亲繁殖不一定会促进利他主义的进化。在生存能力微小差异的假设下,情况要复杂得多,除非假设为加性模型。然而,一般来说,突变等位基因频率初始增加的条件可以根据取决于相互作用个体或其配偶基因型的适合度效应以及根据相互作用个体的近亲繁殖条件的广义条件亲缘系数来获得。