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Genetic variation between long-lived versus short-lived bats illuminates the molecular signatures of longevity

机译:长寿命与短寿蝙蝠之间的遗传变异照亮了长寿的分子签名

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摘要

Bats are the longest-lived mammals given their body size with majority of species exhibiting exceptional longevity. However, there are some short-lived species that do not exhibit extended lifespans. Here we conducted a comparative genomic and transcriptomic study on long-lived (maximum lifespan = 37.1 years) and short-lived (maximum lifespan = 5.6 years) to ascertain the genetic difference underlying their divergent longevities. Genome-wide selection tests on 12,467 single-copy genes between and revealed only three genes ( , and ) that exhibited significant positive selection. Although 97.96% of 12,467 genes underwent purifying selection, we observed a significant heterogeneity in their expression patterns. Using a linear mixed model, we obtained expression of 2,086 genes that may truly represent the genetic difference between and . Expression analysis indicated that long-lived exhibited a transcriptomic profile of enhanced DNA repair and autophagy pathways, compared to . Further investigation of the longevity-associated genes suggested that long-lived have naturally evolved a diminished anti-longevity transcriptomic profile. Together with observations from other long-lived species, our results suggest that heightened DNA repair and autophagy activity may represent a universal mechanism to achieve longevity in long-lived mammals.
机译:蝙蝠是最长的哺乳动物,鉴于它们的体型,大多数物种都表现出出色的寿命。但是,存在一些不表现出延长寿命的短期物种。在这里,我们对长期(最大寿命= 37.1岁)进行了比较基因组和转录组研究,并且短暂的(最大寿命= 5.6岁),以确定其不同寿命的遗传差异。基因组 - 范围的选择测试在12,467个单拷贝基因之间,仅显示出表现出显着阳性选择的三种基因(和)。虽然97.96%的12,467%的基因接受了纯化选择,但我们在表达模式中观察到显着的异质性。使用线性混合模型,我们获得了2,086个基因的表达,可能真正代表与之间的遗传差异。表达分析表明,与百分比相比,长期存在于增强DNA修复和自噬途径的转录组剖面。进一步调查寿命相关基因的进一步调查表明,长期存在的抗寿命转录组剖面自然。我们的结果表明DNA修复和自噬活动中的观察结果以及自噬活动可能代表了在长期哺乳动物中实现寿命的普遍机制。

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