Comparative transcriptomic analysis of the mechanisms underpinning ageing and fecundity in social insects

Author:

Korb Judith1ORCID,Meusemann Karen12ORCID,Aumer Denise3,Bernadou Abel4ORCID,Elsner Daniel1,Feldmeyer Barbara5ORCID,Foitzik Susanne6ORCID,Heinze Jürgen4ORCID,Libbrecht Romain6ORCID,Lin Silu1,Majoe Megha16ORCID,Monroy Kuhn José Manuel1ORCID,Nehring Volker1ORCID,Negroni Matteo A.6,Paxton Robert J.7ORCID,Séguret Alice C.78ORCID,Stoldt Marah6ORCID,Flatt Thomas9ORCID,

Affiliation:

1. Department of Evolutionary Biology and Ecology, Institute of Biology I (Zoology), University of Freiburg, Hauptstraße 1, D-79104 Freiburg (Breisgau), Germany

2. Australian National Insect Collection, CSIRO National Research Collections Australia, Clunies Ross Street, Canberra, Acton 2601, Australia

3. Developmental Zoology, Molecular Ecology Research Group, Hoher Weg 4, D-06099 Halle (Saale), Germany

4. Zoology/Evolutionary Biology, University of Regensburg, Universitätsstraße 31, D-93040 Regensburg, Germany

5. Senckenberg Biodiversity and Climate Research Centre (SBiK-F), Molecular Ecology, Senckenberg, Georg-Voigt-Straße 14-16, D-60325 Frankfurt, Germany

6. Institute of Organismic and Molecular Evolution (IOME), Johannes Gutenberg University Mainz, Hanns-Dieter-Hüsch-Weg 15, D-55128 Mainz, Germany

7. Institute for Biology, Martin Luther University Halle-Wittenberg, Hoher Weg 8, 06120 Halle, Germany

8. Institute for Evolution and Biodiversity, University of Münster, Hüfferstraße 1, 48149 Münster, Germany

9. Department of Biology, University of Fribourg, Chemin du Musée 10, CH-1700 Fribourg, Switzerland

Abstract

The exceptional longevity of social insect queens despite their lifelong high fecundity remains poorly understood in ageing biology. To gain insights into the mechanisms that might underlie ageing in social insects, we compared gene expression patterns between young and old castes (both queens and workers) across different lineages of social insects (two termite, two bee and two ant species). After global analyses, we paid particular attention to genes of the insulin/insulin-like growth factor 1 signalling (IIS)/target of rapamycin (TOR)/juvenile hormone (JH) network, which is well known to regulate lifespan and the trade-off between reproduction and somatic maintenance in solitary insects. Our results reveal a major role of the downstream components and target genes of this network (e.g. JH signalling, vitellogenins, major royal jelly proteins and immune genes) in affecting ageing and the caste-specific physiology of social insects, but an apparently lesser role of the upstream IIS/TOR signalling components. Together with a growing appreciation of the importance of such downstream targets, this leads us to propose the TI–J–LiFe ( T OR/ I IS– J H– Li fespan and Fe cundity) network as a conceptual framework for understanding the mechanisms of ageing and fecundity in social insects and beyond. This article is part of the theme issue ‘Ageing and sociality: why, when and how does sociality change ageing patterns?’

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Deutsche Forschungsgemeinschaft

Novartis Foundation

Publisher

The Royal Society

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

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