Cargando…
Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging
BACKGROUND: Naked mole-rats (NMRs) are eusocially organized in colonies. Although breeders carry the additional metabolic load of reproduction, they are extremely long-lived and remain fertile throughout their lifespan. This phenomenon contrasts the disposable soma theory of aging stating that organ...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090939/ https://www.ncbi.nlm.nih.gov/pubmed/30068345 http://dx.doi.org/10.1186/s12915-018-0546-z |
_version_ | 1783347294138007552 |
---|---|
author | Bens, Martin Szafranski, Karol Holtze, Susanne Sahm, Arne Groth, Marco Kestler, Hans A. Hildebrandt, Thomas B. Platzer, Matthias |
author_facet | Bens, Martin Szafranski, Karol Holtze, Susanne Sahm, Arne Groth, Marco Kestler, Hans A. Hildebrandt, Thomas B. Platzer, Matthias |
author_sort | Bens, Martin |
collection | PubMed |
description | BACKGROUND: Naked mole-rats (NMRs) are eusocially organized in colonies. Although breeders carry the additional metabolic load of reproduction, they are extremely long-lived and remain fertile throughout their lifespan. This phenomenon contrasts the disposable soma theory of aging stating that organisms can invest their resources either in somatic maintenance, enabling a longer lifespan, or in reproduction, at the cost of longevity. Here, we present a comparative transcriptome analysis of breeders vs. non-breeders of the eusocial, long-lived NMR vs. the polygynous and shorter-lived guinea pig (GP). RESULTS: Comparative transcriptome analysis of tissue samples from ten organs showed, in contrast to GPs, low levels of differentiation between sexes in adult NMR non-breeders. After transition into breeders, NMR transcriptomes are markedly sex-specific, show pronounced feedback signaling via gonadal steroids, and have similarities to reproductive phenotypes in African cichlid fish, which also exhibit social status changes between dominant and subordinate phenotypes. Further, NMRs show functional enrichment of status-related expression differences associated with aging. Lipid metabolism and oxidative phosphorylation—molecular networks known to be linked to aging—were identified among most affected gene sets. Remarkably and in contrast to GPs, transcriptome patterns associated with longevity are reinforced in NMR breeders. CONCLUSION: Our results provide comprehensive and unbiased molecular insights into interspecies differences between NMRs and GPs, both in sexual maturation and in the impact of reproduction on longevity. We present molecular evidence that sexual maturation in NMRs is socially suppressed. In agreement with evolutionary theories of aging in eusocial organisms, we have identified transcriptome patterns in NMR breeders that—in contrast to the disposable soma theory of aging—may slow down aging rates and potentially contribute to their exceptional long life- and healthspan. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0546-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6090939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60909392018-08-17 Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging Bens, Martin Szafranski, Karol Holtze, Susanne Sahm, Arne Groth, Marco Kestler, Hans A. Hildebrandt, Thomas B. Platzer, Matthias BMC Biol Research Article BACKGROUND: Naked mole-rats (NMRs) are eusocially organized in colonies. Although breeders carry the additional metabolic load of reproduction, they are extremely long-lived and remain fertile throughout their lifespan. This phenomenon contrasts the disposable soma theory of aging stating that organisms can invest their resources either in somatic maintenance, enabling a longer lifespan, or in reproduction, at the cost of longevity. Here, we present a comparative transcriptome analysis of breeders vs. non-breeders of the eusocial, long-lived NMR vs. the polygynous and shorter-lived guinea pig (GP). RESULTS: Comparative transcriptome analysis of tissue samples from ten organs showed, in contrast to GPs, low levels of differentiation between sexes in adult NMR non-breeders. After transition into breeders, NMR transcriptomes are markedly sex-specific, show pronounced feedback signaling via gonadal steroids, and have similarities to reproductive phenotypes in African cichlid fish, which also exhibit social status changes between dominant and subordinate phenotypes. Further, NMRs show functional enrichment of status-related expression differences associated with aging. Lipid metabolism and oxidative phosphorylation—molecular networks known to be linked to aging—were identified among most affected gene sets. Remarkably and in contrast to GPs, transcriptome patterns associated with longevity are reinforced in NMR breeders. CONCLUSION: Our results provide comprehensive and unbiased molecular insights into interspecies differences between NMRs and GPs, both in sexual maturation and in the impact of reproduction on longevity. We present molecular evidence that sexual maturation in NMRs is socially suppressed. In agreement with evolutionary theories of aging in eusocial organisms, we have identified transcriptome patterns in NMR breeders that—in contrast to the disposable soma theory of aging—may slow down aging rates and potentially contribute to their exceptional long life- and healthspan. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0546-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-02 /pmc/articles/PMC6090939/ /pubmed/30068345 http://dx.doi.org/10.1186/s12915-018-0546-z Text en © Bens et al. 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Bens, Martin Szafranski, Karol Holtze, Susanne Sahm, Arne Groth, Marco Kestler, Hans A. Hildebrandt, Thomas B. Platzer, Matthias Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging |
title | Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging |
title_full | Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging |
title_fullStr | Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging |
title_full_unstemmed | Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging |
title_short | Naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging |
title_sort | naked mole-rat transcriptome signatures of socially suppressed sexual maturation and links of reproduction to aging |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090939/ https://www.ncbi.nlm.nih.gov/pubmed/30068345 http://dx.doi.org/10.1186/s12915-018-0546-z |
work_keys_str_mv | AT bensmartin nakedmolerattranscriptomesignaturesofsociallysuppressedsexualmaturationandlinksofreproductiontoaging AT szafranskikarol nakedmolerattranscriptomesignaturesofsociallysuppressedsexualmaturationandlinksofreproductiontoaging AT holtzesusanne nakedmolerattranscriptomesignaturesofsociallysuppressedsexualmaturationandlinksofreproductiontoaging AT sahmarne nakedmolerattranscriptomesignaturesofsociallysuppressedsexualmaturationandlinksofreproductiontoaging AT grothmarco nakedmolerattranscriptomesignaturesofsociallysuppressedsexualmaturationandlinksofreproductiontoaging AT kestlerhansa nakedmolerattranscriptomesignaturesofsociallysuppressedsexualmaturationandlinksofreproductiontoaging AT hildebrandtthomasb nakedmolerattranscriptomesignaturesofsociallysuppressedsexualmaturationandlinksofreproductiontoaging AT platzermatthias nakedmolerattranscriptomesignaturesofsociallysuppressedsexualmaturationandlinksofreproductiontoaging |