Leips Jeff, Gilligan Paul, Mackay Trudy F C
Department of Biological Sciences, University of Maryland Baltimore County, Baltimore 21250, USA.
Genetics. 2006 Mar;172(3):1595-605. doi: 10.1534/genetics.105.048520. Epub 2005 Nov 4.
Life-history theory and evolutionary theories of aging assume the existence of alleles with age-specific effects on fitness. While various studies have documented age-related changes in the genetic contribution to variation in fitness components, we know very little about the underlying genetic architecture of such changes. We used a set of recombinant inbred lines to map and characterize the effects of quantitative trait loci (QTL) affecting fecundity of Drosophila melanogaster females at 1 and 4 weeks of age. We identified one QTL on the second chromosome and one or two QTL affecting fecundity on the third chromosome, but these QTL affected fecundity only at 1 week of age. There was more genetic variation for fecundity at 4 weeks of age than at 1 week of age and there was no genetic correlation between early and late-age fecundity. These results suggest that different loci contribute to the variation in fecundity as the organism ages. Our data provide support for the mutation accumulation theory of aging as applied to reproductive senescence. Comparing the results from this study with our previous work on life-span QTL, we also find evidence that antagonistic pleiotropy may contribute to the genetic basis of senescence in these lines as well.
生活史理论和衰老进化论假定存在对适合度有年龄特异性效应的等位基因。虽然各种研究记录了与年龄相关的适合度成分变异的遗传贡献变化,但我们对这些变化的潜在遗传结构知之甚少。我们使用一组重组近交系来定位和表征影响黑腹果蝇雌性在1周龄和4周龄时繁殖力的数量性状基因座(QTL)的效应。我们在第二条染色体上鉴定出一个QTL,在第三条染色体上鉴定出一个或两个影响繁殖力的QTL,但这些QTL仅在1周龄时影响繁殖力。4周龄时繁殖力的遗传变异比1周龄时更多,且早期和晚期繁殖力之间没有遗传相关性。这些结果表明,随着生物体衰老,不同的基因座对繁殖力变异有贡献。我们的数据为应用于生殖衰老的衰老突变积累理论提供了支持。将本研究结果与我们之前关于寿命QTL的工作进行比较,我们还发现有证据表明拮抗多效性也可能是这些品系衰老遗传基础的一部分。