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Long-lived Temnothorax ant queens switch from investment in immunity to antioxidant production with age
Senescence is manifested by an increase in molecular damage and a deterioration of biological functions with age. In most organisms, body maintenance is traded-off with reproduction. This negative relationship between longevity and fecundity is also evident on the molecular level. Exempt from this n...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514213/ https://www.ncbi.nlm.nih.gov/pubmed/31086243 http://dx.doi.org/10.1038/s41598-019-43796-1 |
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author | Negroni, Matteo Antoine Foitzik, Susanne Feldmeyer, Barbara |
author_facet | Negroni, Matteo Antoine Foitzik, Susanne Feldmeyer, Barbara |
author_sort | Negroni, Matteo Antoine |
collection | PubMed |
description | Senescence is manifested by an increase in molecular damage and a deterioration of biological functions with age. In most organisms, body maintenance is traded-off with reproduction. This negative relationship between longevity and fecundity is also evident on the molecular level. Exempt from this negative trait association, social insect queens are both extremely long-lived and highly fecund. Here, we study changes in gene expression with age and fecundity in ant queens to understand the molecular basis of their long lifespan. We analyse tissue-specific gene expression in young founding queens and old fecund queens of the ant Temnothorax rugatulus. More genes altered their expression with age in the fat body than in the brain. Despite strong differences in ovary development, few fecundity genes were differentially expressed. Young founding queens invested in immunity (i.e. activation of Toll signalling pathway) and resistance against environmental and physiological stress (i.e. down-regulation of TOR pathway). Conversely, established older queens invested into anti-aging mechanisms through an overproduction of antioxidants (i.e. upregulation of catalase, superoxide dismutase). Finally, we identified candidate genes and pathways, potentially involved in the association between fertility and longevity in social insects and its proximate basis. |
format | Online Article Text |
id | pubmed-6514213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65142132019-05-24 Long-lived Temnothorax ant queens switch from investment in immunity to antioxidant production with age Negroni, Matteo Antoine Foitzik, Susanne Feldmeyer, Barbara Sci Rep Article Senescence is manifested by an increase in molecular damage and a deterioration of biological functions with age. In most organisms, body maintenance is traded-off with reproduction. This negative relationship between longevity and fecundity is also evident on the molecular level. Exempt from this negative trait association, social insect queens are both extremely long-lived and highly fecund. Here, we study changes in gene expression with age and fecundity in ant queens to understand the molecular basis of their long lifespan. We analyse tissue-specific gene expression in young founding queens and old fecund queens of the ant Temnothorax rugatulus. More genes altered their expression with age in the fat body than in the brain. Despite strong differences in ovary development, few fecundity genes were differentially expressed. Young founding queens invested in immunity (i.e. activation of Toll signalling pathway) and resistance against environmental and physiological stress (i.e. down-regulation of TOR pathway). Conversely, established older queens invested into anti-aging mechanisms through an overproduction of antioxidants (i.e. upregulation of catalase, superoxide dismutase). Finally, we identified candidate genes and pathways, potentially involved in the association between fertility and longevity in social insects and its proximate basis. Nature Publishing Group UK 2019-05-13 /pmc/articles/PMC6514213/ /pubmed/31086243 http://dx.doi.org/10.1038/s41598-019-43796-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Negroni, Matteo Antoine Foitzik, Susanne Feldmeyer, Barbara Long-lived Temnothorax ant queens switch from investment in immunity to antioxidant production with age |
title | Long-lived Temnothorax ant queens switch from investment in immunity to antioxidant production with age |
title_full | Long-lived Temnothorax ant queens switch from investment in immunity to antioxidant production with age |
title_fullStr | Long-lived Temnothorax ant queens switch from investment in immunity to antioxidant production with age |
title_full_unstemmed | Long-lived Temnothorax ant queens switch from investment in immunity to antioxidant production with age |
title_short | Long-lived Temnothorax ant queens switch from investment in immunity to antioxidant production with age |
title_sort | long-lived temnothorax ant queens switch from investment in immunity to antioxidant production with age |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514213/ https://www.ncbi.nlm.nih.gov/pubmed/31086243 http://dx.doi.org/10.1038/s41598-019-43796-1 |
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