Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite

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dc.contributor.author Seite, Sarah
dc.contributor.author Harrison, Mark C.
dc.contributor.author Sillam-Dusses, David
dc.contributor.author Lupoli, Roland
dc.contributor.author Van Dooren, Tom J.M.
dc.contributor.author Robert, Alain
dc.contributor.author Poissonnier, Laure-Anne
dc.contributor.author Lemainque, Arnaud
dc.contributor.author Renault, David
dc.contributor.author Acket, Sebastien
dc.contributor.author Andrieu, Muriel
dc.contributor.author Viscarra, Jose
dc.contributor.author Sul, Hei Sook
dc.contributor.author De Beer, Z. Wilhelm
dc.contributor.author Bornberg-Bauer, Erich
dc.contributor.author Vasseur-Cognet, Mireille
dc.date.accessioned 2022-01-31T11:41:18Z
dc.date.available 2022-01-31T11:41:18Z
dc.date.issued 2022-01
dc.description.abstract Kings and queens of eusocial termites can live for decades, while queens sustain a nearly maximal fertility. To investigate the molecular mechanisms underlying their long lifespan, we carried out transcriptomics, lipidomics and metabolomics in Macrotermes natalensis on sterile short-lived workers, long-lived kings and five stages spanning twenty years of adult queen maturation. Reproductives share gene expression differences from workers in agreement with a reduction of several aging-related processes, involving upregulation of DNA damage repair and mitochondrial functions. Anti-oxidant gene expression is downregulated, while peroxidability of membranes in queens decreases. Against expectations, we observed an upregulated gene expression in fat bodies of reproductives of several components of the IIS pathway, including an insulin-like peptide, Ilp9. This pattern does not lead to deleterious fat storage in physogastric queens, while simple sugars dominate in their hemolymph and large amounts of resources are allocated towards oogenesis. Our findings support the notion that all processes causing aging need to be addressed simultaneously in order to prevent it. en_ZA
dc.description.department Biochemistry en_ZA
dc.description.department Forestry and Agricultural Biotechnology Institute (FABI) en_ZA
dc.description.department Genetics en_ZA
dc.description.department Microbiology and Plant Pathology en_ZA
dc.description.librarian hj2022 en_ZA
dc.description.sponsorship The International Human Frontier Science Program RGP0060/2018; a fellowship from Université de Paris Est-Créteil (UPEC) and France Génomique (ANR-10-INBS-09-08). en_ZA
dc.description.uri https://www.nature.com/commsbio en_ZA
dc.identifier.citation Séité, S., Harrison, M.C., Sillam-Dussès, D. et al. Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite. Communications Biology 5, 44 (2022). https://doi.org/10.1038/s42003-021-02974-6. en_ZA
dc.identifier.issn 2399-3642 (online)
dc.identifier.other 10.1038/s42003-021-02974-6
dc.identifier.uri http://hdl.handle.net/2263/83536
dc.language.iso en en_ZA
dc.publisher Nature Publishing en_ZA
dc.rights © The Author(s) 2021. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License. en_ZA
dc.subject Ageing en_ZA
dc.subject Metabolism en_ZA
dc.title Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite en_ZA
dc.type Article en_ZA


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