Tobias Møgelvang Nielsen, Jaden Baldwin, Megan Danis, Kenneth M. Fedorka
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If Y-chromosomes instead compensate by modifying autosomal targets (or its elucidation requires coevolved autosomes), then this design could fail to detect Y-compensation. Here we address if Y-chromosomes ameliorate mitochondrial mutations affecting male lifespan in Drosophila melanogaster. Using three disparate populations we compared lifespan among males with coevolved and non-coevolved Y-mitochondria pairs placed alongside autosomal backgrounds coevolved with mitochondria. We found coevolved pairs exhibited lower mortality risk relative to non-coevolved pairs. In contrast, no such pattern was observed when coevolved and non-coevolved pairs were placed alongside non-coevolved autosomes, as with previous studies. These data are consistent with Y-compensation and highlight the importance of autosomes in this capacity. However, we cannot fully exclude the possibility that Y-autosomal coevolution independent of mitochondrial mutations contributed to our results. 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引用次数: 0
摘要
母亲的诅咒指的是由于线粒体严格的母系遗传而可能在线粒体上积累的偏向男性的有害突变。如果这些突变持续存在,鉴于Y染色体严格的父系遗传,男性最好通过Y染色体上的突变进行补偿。以前的研究通过比较共同进化和非共同进化的 Y 线粒体配对与完全外来的常染色体背景,预期共同进化配对的雄性个体会因 Y 补偿而表现出更强的适应性,从而解决了这一假设。迄今为止,尚未发现 Y 补偿的证据。这种实验设计假设 Y 染色体通过与线粒体和/或共同进化的常染色体的直接相互作用进行补偿,但这对其功能或阐明并不重要。如果 Y 染色体是通过改变常染色体靶标来进行补偿(或其阐明需要共同进化的常染色体),那么这种设计可能无法检测到 Y 补偿。在这里,我们探讨了 Y 染色体是否能改善影响黑腹果蝇雄性寿命的线粒体突变。我们利用三个不同的种群,比较了与线粒体共同进化的常染色体背景同时存在的Y-线粒体配对与非共同进化的Y-线粒体配对的雄性果蝇的寿命。我们发现,与非共同进化的配对相比,共同进化的配对表现出较低的死亡风险。相比之下,将共同进化和非共同进化的基因对与非共同进化的常染色体放在一起时,则没有观察到这种模式,这与之前的研究相同。这些数据与 Y 补偿一致,并突出了常染色体在这一能力中的重要性。但是,我们不能完全排除线粒体突变之外的 Y 常染色体共同进化对我们的研究结果产生影响的可能性。无论如何,将外来 Y 染色体引入非共同进化背景的现代医学、保护和农业实践应谨慎使用,因为它们可能会破坏 Y-常染色体共同适应和/或无意中解除母亲的诅咒。
Support for Y-compensation of mother’s curse affecting lifespan in Drosophila melanogaster
Mother’s curse refers to male-biased deleterious mutations that may accumulate on mitochondria due to its strict maternal inheritance. If these mutations persist, males should ideally compensate through mutations on Y-chromosomes given its strict paternal inheritance. Previous work addressed this hypothesis by comparing coevolved and non-coevolved Y-mitochondria pairs placed alongside completely foreign autosomal backgrounds, expecting males with coevolved pairs to exhibit greater fitness due to Y-compensation. To date, no evidence for Y-compensation has been found. That experimental design assumes Y-chromosomes compensate via direct interaction with mitochondria and/or coevolved autosomes are unimportant in its function or elucidation. If Y-chromosomes instead compensate by modifying autosomal targets (or its elucidation requires coevolved autosomes), then this design could fail to detect Y-compensation. Here we address if Y-chromosomes ameliorate mitochondrial mutations affecting male lifespan in Drosophila melanogaster. Using three disparate populations we compared lifespan among males with coevolved and non-coevolved Y-mitochondria pairs placed alongside autosomal backgrounds coevolved with mitochondria. We found coevolved pairs exhibited lower mortality risk relative to non-coevolved pairs. In contrast, no such pattern was observed when coevolved and non-coevolved pairs were placed alongside non-coevolved autosomes, as with previous studies. These data are consistent with Y-compensation and highlight the importance of autosomes in this capacity. However, we cannot fully exclude the possibility that Y-autosomal coevolution independent of mitochondrial mutations contributed to our results. Regardless, modern practices in medicine, conservation, and agriculture that introduce foreign Y-chromosomes into non-coevolved backgrounds should be used with caution, as they may disrupt Y-autosome coadaptation and/or inadvertently unbridle mother’s curse.
期刊介绍:
Heredity is the official journal of the Genetics Society. It covers a broad range of topics within the field of genetics and therefore papers must address conceptual or applied issues of interest to the journal''s wide readership