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沉默调节蛋白不是保守的长寿基因。

Sirtuins are Not Conserved Longevity Genes.

作者信息

Brenner Charles

机构信息

Department of Diabetes & Cancer Metabolism, Beckman Research Institute of City of Hope, Duarte, CA 91010 USA.

出版信息

Life Metab. 2022 Oct;1(2):122-133. doi: 10.1093/lifemeta/loac025. Epub 2022 Sep 22.

Abstract

It is central to biology that sequence conservation suggests functional conservation. Animal longevity is an emergent property of selected traits that integrates capacities to perform physical and mental functions after reproductive maturity. Though the yeast gene was nominated as a longevity gene based on extended replicative longevity of old mother cells, this is not a selected trait: is selected against in chronological aging and the direct targets of in replicative lifespan are not conserved. Though it would be difficult to imagine how a gene that advantages 1 in 5 million yeast cells could have anticipated causes of aging in animals, overexpression of homologs was tested in invertebrates for longevity. Because artifactual positive results were reported years before they were sorted out and because it was not known that functions as a pro-aging gene in yeast chronological aging and in flies subject to amino acid deprivation, a global pursuit of longevity phenotypes was driven by a mixture of framing bias, confirmation bias and hype. Review articles that propagate these biases are so rampant that few investigators have considered how weak the case ever was for sirtuins as longevity genes. Acknowledging that a few positive associations between sirtuins and longevity have been identified after thousands of person-years and billions of dollars of effort, we review the data and suggest rejection of the notions that sirtuins 1) have any specific connection to lifespan in animals and 2) are primary mediators of the beneficial effects of NAD repletion.

摘要

序列保守性暗示功能保守性,这是生物学的核心内容。动物的长寿是特定性状的一种涌现特性,它整合了生殖成熟后执行身体和心理功能的能力。尽管酵母基因基于老龄母细胞延长的复制寿命被提名为长寿基因,但这并非一个被选择的性状:在时序衰老过程中它是被选择淘汰的,并且在复制寿命中它的直接靶点并不保守。尽管很难想象一个对五百万个酵母细胞中的一个有益的基因能够预测动物衰老的原因,但还是在无脊椎动物中测试了其同源物的过表达对寿命的影响。由于在问题得到解决的数年前就报道了人为造成的阳性结果,并且由于当时尚不清楚该基因在酵母时序衰老和遭受氨基酸剥夺的果蝇中作为促衰老基因发挥作用,对长寿表型的全球研究受到了框架偏差、确认偏差和炒作的综合驱动。传播这些偏差的综述文章非常普遍,以至于很少有研究者思考过将沉默调节蛋白作为长寿基因的证据有多薄弱。在经过数千人年的努力和数十亿美元的投入后,我们承认已经确定了沉默调节蛋白与长寿之间的一些阳性关联,在此我们审视相关数据,并建议摒弃以下观点:1)沉默调节蛋白与动物寿命有任何特定联系;2)它们是NAD补充有益作用的主要介导者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6f6/11749623/36212b3af653/loac025_fig1.jpg

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