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寿命和衰老过程中性别差异的演变:原因和限制。

Evolution of sex differences in lifespan and aging: causes and constraints.

机构信息

Department of Animal Ecology, Evolutionary Biology Centre, Uppsala University, Uppsala, Sweden.

出版信息

Bioessays. 2013 Aug;35(8):717-24. doi: 10.1002/bies.201300021. Epub 2013 Jun 3.

Abstract

Why do the two sexes have different lifespans and rates of aging? Two hypotheses based on asymmetric inheritance of sex chromosomes ("unguarded X") or mitochondrial genomes ("mother's curse") explain sex differences in lifespan as sex-specific maladaptation leading to increased mortality in the shorter-lived sex. While asymmetric inheritance hypotheses equate long life with high fitness, considerable empirical evidence suggests that sexes resolve the fundamental tradeoff between reproduction and survival differently resulting in sex-specific optima for lifespan. However, selection for sex-specific values in life-history traits is constrained by intersexual genetic correlations resulting in intra-locus sexual conflict over optimal lifespan. The available data suggest that the evolution of sexual dimorphism only partially resolves these conflicts. Sexual conflict over optimal trait values, which has been demonstrated in model organisms and in humans, is likely to play a key role in shaping the evolution of lifespan, as well as in maintaining genetic variation for sex-specific diseases.

摘要

为什么两性的寿命和衰老速度不同?两种基于性染色体非对称遗传(“无保护的 X”)或线粒体基因组(“母亲的诅咒”)的假说解释了寿命的性别差异,认为这是导致寿命较短的性别死亡率增加的性别特异性适应不良。虽然非对称遗传假说将长寿等同于高适应性,但大量经验证据表明,性别以不同的方式解决了繁殖和生存之间的基本权衡,从而导致了寿命的性别特异性最佳值。然而,对生活史特征的性别特异性值的选择受到性间遗传相关性的限制,从而导致了寿命的局域性性冲突。现有数据表明,性二态性的进化只能部分解决这些冲突。在模型生物和人类中已经证明,对最佳特征值的性冲突很可能在塑造寿命进化以及维持性别特异性疾病的遗传变异性方面发挥关键作用。

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