Reynolds Rose M, Temiyasathit Sara, Reedy Melissa M, Ruedi Elizabeth A, Drnevich Jenny M, Leips Jeff, Hughes Kimberly A
Program in Ecology and Evolutionary Biology, University of Illinois, Urbana-Champaign, Illinois 61801, USA.
Genetics. 2007 Sep;177(1):587-95. doi: 10.1534/genetics.106.070078. Epub 2007 Jul 29.
Current evolutionary theories explain the origin of aging as a byproduct of the decline in the force of natural selection with age. These theories seem inconsistent with the well-documented occurrence of late-life mortality plateaus, since under traditional evolutionary models mortality rates should increase monotonically after sexual maturity. However, the equilibrium frequencies of deleterious alleles affecting late life are lower than predicted under traditional models, and thus evolutionary models can accommodate mortality plateaus if deleterious alleles are allowed to have effects spanning a range of neighboring age classes. Here we test the degree of age specificity of segregating alleles affecting fitness in Drosophila melanogaster. We assessed age specificity by measuring the homozygous fitness effects of segregating alleles across the adult life span and calculated genetic correlations of these effects across age classes. For both males and females, we found that allelic effects are age specific with effects extending over 1-2 weeks across all age classes, consistent with modified mutation-accumulation theory. These results indicate that a modified mutation-accumulation theory can both explain the origin of senescence and predict late-life mortality plateaus.
当前的进化理论将衰老的起源解释为自然选择力随年龄下降的副产品。这些理论似乎与充分记录的晚年死亡率平稳现象不一致,因为在传统进化模型下,死亡率在性成熟后应单调增加。然而,影响晚年的有害等位基因的平衡频率低于传统模型的预测,因此,如果允许有害等位基因对一系列相邻年龄组产生影响,进化模型可以解释死亡率平稳现象。在这里,我们测试了影响黑腹果蝇适应性的分离等位基因的年龄特异性程度。我们通过测量成年期整个寿命中分离等位基因的纯合适应性效应来评估年龄特异性,并计算这些效应在不同年龄组之间的遗传相关性。对于雄性和雌性,我们发现等位基因效应具有年龄特异性,且在所有年龄组中效应持续1 - 2周,这与修正的突变积累理论一致。这些结果表明,修正的突变积累理论既能解释衰老的起源,又能预测晚年死亡率平稳现象。