Juan Jose Alba-Linares, Juan Ramon Tejedor, Agustin F. Fernandez, Raul F. Perez, Mario F. Fraga
{"title":"表观遗传熵揭示哺乳动物寿命的普遍极限","authors":"Juan Jose Alba-Linares, Juan Ramon Tejedor, Agustin F. Fernandez, Raul F. Perez, Mario F. Fraga","doi":"10.1101/2024.09.06.611669","DOIUrl":null,"url":null,"abstract":"Age-associated DNA methylation patterns have shown strong associations with species lifespan. However, it remains unclear whether epigenetic noise levels can account for the observed differences between mammalian species. In this study, we examined the rate of loss of epigenetic information with age by measuring entropy at mammalian conserved CpG sites across a diverse range of species. Longer-lived mammals tend to gain fewer noisy CpGs with age, irrespective of whether these originate from hyper- or hypomethylation processes. Importantly, we found that the rate of epigenetic entropy gain declines in a linear fashion with species maximum lifespan, pointing to the existence of a universal limit for mammalian lifespan in the vicinity of 220 years.","PeriodicalId":501108,"journal":{"name":"bioRxiv - Molecular Biology","volume":"110 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A universal limit for mammalian lifespan revealed by epigenetic entropy\",\"authors\":\"Juan Jose Alba-Linares, Juan Ramon Tejedor, Agustin F. Fernandez, Raul F. Perez, Mario F. Fraga\",\"doi\":\"10.1101/2024.09.06.611669\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Age-associated DNA methylation patterns have shown strong associations with species lifespan. However, it remains unclear whether epigenetic noise levels can account for the observed differences between mammalian species. In this study, we examined the rate of loss of epigenetic information with age by measuring entropy at mammalian conserved CpG sites across a diverse range of species. Longer-lived mammals tend to gain fewer noisy CpGs with age, irrespective of whether these originate from hyper- or hypomethylation processes. Importantly, we found that the rate of epigenetic entropy gain declines in a linear fashion with species maximum lifespan, pointing to the existence of a universal limit for mammalian lifespan in the vicinity of 220 years.\",\"PeriodicalId\":501108,\"journal\":{\"name\":\"bioRxiv - Molecular Biology\",\"volume\":\"110 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"bioRxiv - Molecular Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.09.06.611669\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.09.06.611669","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
年龄相关的 DNA 甲基化模式与物种的寿命密切相关。然而,目前仍不清楚表观遗传噪音水平是否能解释哺乳动物物种间观察到的差异。在这项研究中,我们通过测量不同物种哺乳动物保守 CpG 位点的熵,考察了表观遗传信息随年龄增长的丢失率。寿命较长的哺乳动物往往随着年龄的增长而获得较少的噪声 CpGs,无论这些噪声是来自超甲基化还是低甲基化过程。重要的是,我们发现表观遗传熵增率随着物种最长寿命的增长呈线性下降,这表明哺乳动物的普遍寿命极限在 220 岁左右。
A universal limit for mammalian lifespan revealed by epigenetic entropy
Age-associated DNA methylation patterns have shown strong associations with species lifespan. However, it remains unclear whether epigenetic noise levels can account for the observed differences between mammalian species. In this study, we examined the rate of loss of epigenetic information with age by measuring entropy at mammalian conserved CpG sites across a diverse range of species. Longer-lived mammals tend to gain fewer noisy CpGs with age, irrespective of whether these originate from hyper- or hypomethylation processes. Importantly, we found that the rate of epigenetic entropy gain declines in a linear fashion with species maximum lifespan, pointing to the existence of a universal limit for mammalian lifespan in the vicinity of 220 years.