The androgen clock is an epigenetic predictor of long- term male hormone exposure

被引:1
|
作者
Sugrue, Victoria J. [1 ]
Prescott, Melanie [2 ]
Glendining, Kelly A. [2 ]
Bond, Donna M. [1 ]
Horvath, Steve [3 ,4 ]
Anderson, Greg M. [1 ]
Garratt, Michael [1 ]
Campbell, Rebecca E. [2 ]
Hore, Timothy A. [1 ]
机构
[1] Univ Otago, Dept Anat, Dunedin 9016, New Zealand
[2] Univ Otago, Dept Physiol, Dunedin 9016, New Zealand
[3] Cambridge Inst Sci, Altos Labs, Cambridge CB21 6GQ, England
[4] Univ Calif Los Angeles, Fielding Sch Publ Hlth, Dept Biostat, Los Angeles, CA 90095 USA
关键词
epigenetics; aging; ageing; androgens; epigenetic clock; LIFE-SPAN; DNA METHYLATION; ANABOLIC-STEROIDS; TESTOSTERONE; MORTALITY; BEHAVIOR; LONGEVITY; ESTRADIOL; SURVIVAL; RECEPTOR;
D O I
10.1073/pnas.2420087121
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
Aging is a complex process characterized by biological decline and a wide range of molecular alterations to cells, including changes to DNA methylation. In this study, we used a male- specific epigenetic marker of aging to build an epigenetic predictor that measures long- term androgen exposure in sheep and mice (median absolute error of 4.3 and 1.4 mo, respectively). We term this predictor the androgen clock and show its "tick" is mediated by the androgen receptor and can be accelerated beyond that in normal male mice by supplementing females with dihydrotestosterone. Conversely, the removal of androgens by castration in sheep completely halted the androgen clock. In addition to potential applications in medicine and agriculture, we predict the androgen clock will prove a useful model to understand the mechanisms and processes of age- associated molecule manipulation with few additional effects on the cell.
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收藏
页数:9
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