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性相关的衰老速度差异与两栖动物的性染色体系统有关。

Sex-related differences in aging rate are associated with sex chromosome system in amphibians.

机构信息

Department of Ecology and Evolution, University of Lausanne, Lausanne, 1015, Switzerland.

Laboratoire de Biométrie et Biologie Evolutive, Université Lyon 1, CNRS, UMR 5558, Villeurbanne, F-769622, France.

出版信息

Evolution. 2022 Feb;76(2):346-356. doi: 10.1111/evo.14410. Epub 2022 Jan 7.

Abstract

Sex-related differences in mortality are widespread in the animal kingdom. Although studies have shown that sex determination systems might drive lifespan evolution, sex chromosome influence on aging rates have not been investigated so far, likely due to an apparent lack of demographic data from clades including both XY (with heterogametic males) and ZW (heterogametic females) systems. Taking advantage of a unique collection of capture-recapture datasets in amphibians, a vertebrate group where XY and ZW systems have repeatedly evolved over the past 200 million years, we examined whether sex heterogamy can predict sex differences in aging rates and lifespans. We showed that the strength and direction of sex differences in aging rates (and not lifespan) differ between XY and ZW systems. Sex-specific variation in aging rates was moderate within each system, but aging rates tended to be consistently higher in the heterogametic sex. This led to small but detectable effects of sex chromosome system on sex differences in aging rates in our models. Although preliminary, our results suggest that exposed recessive deleterious mutations on the X/Z chromosome (the "unguarded X/Z effect") or repeat-rich Y/W chromosome (the "toxic Y/W effect") could accelerate aging in the heterogametic sex in some vertebrate clades.

摘要

性别相关的死亡率差异在动物界中广泛存在。尽管研究表明性别决定系统可能会驱动寿命进化,但迄今为止,性染色体对衰老速度的影响尚未得到研究,这可能是由于缺乏包括 XY(异型雄性)和 ZW(异型雌性)系统在内的进化枝的人口统计数据。利用两栖动物独特的捕获-再捕获数据集,我们检查了性别异型是否可以预测衰老速度和寿命的性别差异。我们发现,在 XY 和 ZW 系统中,衰老速度的性别差异的强度和方向不同。每个系统内的性别特异性衰老速度变化适中,但在异型性别的衰老速度往往更高。这导致我们的模型中,性染色体系统对衰老速度性别差异的影响虽小但可检测。尽管初步的,但我们的研究结果表明,暴露的隐性有害突变在 X/Z 染色体上(“无保护的 X/Z 效应”)或富含重复的 Y/W 染色体上(“有毒的 Y/W 效应”)可能会加速某些脊椎动物进化枝中异型性别的衰老。

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