Comparative analyses of aging-related genes in long-lived mammals provide insights into natural longevity

被引:17
作者
Yu, Zhenpeng [1 ]
Seim, Inge [1 ,2 ,3 ]
Yin, Mengxin [1 ]
Tian, Ran [1 ]
Sun, Di [1 ]
Ren, Wenhua [1 ]
Yang, Guang [1 ]
Xu, Shixia [1 ]
机构
[1] Nanjing Normal Univ, Coll Life Sci, Jiangsu Key Lab Biodivers & Biotechnol, Nanjing 210023, Peoples R China
[2] Nanjing Normal Univ, Coll Life Sci, Integrat Biol Lab, Nanjing 210023, Peoples R China
[3] Queensland Univ Technol, Fac Sci & Engn, Sch Biol & Environm Sci, Brisbane, Qld, Australia
来源
INNOVATION | 2021年 / 2卷 / 02期
基金
中国国家自然科学基金;
关键词
mammals; longevity; positive selection; IIS pathway; immune response; cancer resistance; LIFE-SPAN EXTENSION; NAKED MOLE-RAT; CANCER RESISTANCE; EVOLUTION; RECEPTOR; NETWORK; CELL; AGE; P53;
D O I
10.1016/j.xinn.2021.100108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extreme longevity has evolved multiple times during the evolution of mammals, yet its underlying molecular mechanisms remain largely underexplored. Here, we compared the evolution of 115 aging-related genes in 11 long-lived species and 25 mammals with non-increased lifespan (control group) in the hopes of better understanding the common molecular mechanisms behind longevity. We identified 16 unique positively selected genes and 23 rapidly evolving genes in long-lived species, which included nine genes involved in regulating lifespan through the insulin/IGF-1 signaling (IIS) pathway and 11 genes highly enriched in immune-response-related pathways, suggesting that the IIS pathway and immune response play a particularly important role in exceptional mammalian longevity. Interestingly, 11 genes related to cancer progression, including four positively selected genes and seven genes with convergent amino acid changes, were shared by two or more long-lived lineages, indicating that long-lived mammals might have evolved convergent or similar mechanisms of cancer resistance that extended their lifespan. This suggestion was further corroborated by our identification of 12 robust candidates for longevity-related genes closely related to cancer.
引用
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页数:9
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