Charlesworth B
Institute for Cell, Animal and Population Biology, University of Edinburgh, King's Buildings, Edinburgh, EH9 3JT, UK.
J Theor Biol. 2001 May 7;210(1):47-65. doi: 10.1006/jtbi.2001.2296.
A general quantitative genetic model of mutations with age-specific deleterious effects is developed. It is shown that, for the simplest case of a species with age-independent reproductive rates and extrinsic adult mortality rates, and no pleiotropic effects of age-specific mutations, exponential increases with age of both the mean and additive genetic variance of age-specific mortality rates are expected. Models where age-specific mutations have pleiotropic effects on mortality that extend either throughout adult life, or are confined to juvenile stages, produce equilibria with exponential increases in the mean and additive variance of mortality rates during much of adult life. However, the rates of increase diminish late in life, and can even become zero. Predictions concerning the additive genetic correlations in mortality rates between different ages are also developed. The predictions of the models are compared with data on humans and Drosophila.
建立了一个具有年龄特异性有害效应的突变的一般定量遗传模型。结果表明,对于具有与年龄无关的繁殖率和外在成年死亡率且年龄特异性突变无多效性效应的最简单物种情况,预期年龄特异性死亡率的均值和加性遗传方差均会随年龄呈指数增长。年龄特异性突变对死亡率具有多效性效应的模型,这些效应要么贯穿成年期,要么局限于幼年期,在成年期的大部分时间里会产生死亡率均值和加性方差呈指数增长的平衡状态。然而,增长率在生命后期会降低,甚至可能变为零。还得出了关于不同年龄之间死亡率加性遗传相关性的预测。将模型的预测结果与人类和果蝇的数据进行了比较。