When does early‐life telomere length predict survival? A case study and meta‐analysis

Author:

Eastwood Justin R.1ORCID,Dupoué Andréaz12ORCID,Delhey Kaspar13ORCID,Verhulst Simon4ORCID,Cockburn Andrew5ORCID,Peters Anne16ORCID

Affiliation:

1. School of Biological Sciences Monash University Clayton Victoria Australia

2. CNRS Sorbonne Université, UMR 7618, iEES Paris Université Pierre et Marie Curie Paris France

3. Department Behavioural Ecology & Evolutionary Genetics Max Planck Institute for Ornithology Seewiesen Germany

4. Groningen Institute for Evolutionary Life Sciences University of Groningen Groningen The Netherlands

5. Division of Ecology and Evolution, Research School of Biology The Australian National University Canberra Australian Capital Territory Australia

6. Max Planck Institute for Ornithology, Vogelwarte Radolfzell Radolfzell Germany

Abstract

AbstractSuboptimal conditions during development can shorten telomeres, the protective DNA caps on the end of chromosomes. Shorter early‐life telomere length (TL) can indicate reduced somatic maintenance, leading to lower survival and shorter lifespan. However, despite some clear evidence, not all studies show a relationship between early‐life TL and survival or lifespan, which may be due to differences in biology or study design (e.g., survival period measured). In superb fairy‐wrens (Malurus cyaneus), we assessed whether early‐life TL predicts mortality across different life‐history stages (fledgling, juvenile, adult). However, in contrast to a similar study on a congener, early‐life TL did not predict mortality across any life stage in this species. We then performed a meta‐analysis including 32 effect sizes from 23 studies (15 birds and three mammals) to quantify the effect of early‐life TL on mortality whilst taking into consideration potential sources of biological and methodological variation. Overall, the effect of early‐life TL on mortality was significant, corresponding to a 15% reduction in mortality risk with each standard deviation increase in TL. However, the effect became weaker when correcting for publication bias. Contrary to our predictions, there was no evidence that effects of early‐life TL on mortality varied with species lifespan or the period over which survival was measured. However, negative effects of early‐life TL on mortality risk were pervasive throughout life. These results imply that effects of early‐life TL on mortality are more likely to be context‐dependent than age‐dependent, although substantial power and publication bias issues highlight the need for more research.

Funder

Australian Research Council

Publisher

Wiley

Subject

Genetics,Ecology, Evolution, Behavior and Systematics

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3