Cargando…

Telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (Glis glis)

Telomere shortening is thought to be an important biomarker for life history traits such as lifespan and aging, and can be indicative of genome integrity, survival probability and the risk of cancer development. In humans and other animals, telomeres almost always shorten with age, with more rapid t...

Descripción completa

Detalles Bibliográficos
Autores principales: Hoelzl, Franz, Smith, Steve, Cornils, Jessica S., Aydinonat, Denise, Bieber, Claudia, Ruf, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121655/
https://www.ncbi.nlm.nih.gov/pubmed/27883035
http://dx.doi.org/10.1038/srep36856
_version_ 1782469453084098560
author Hoelzl, Franz
Smith, Steve
Cornils, Jessica S.
Aydinonat, Denise
Bieber, Claudia
Ruf, Thomas
author_facet Hoelzl, Franz
Smith, Steve
Cornils, Jessica S.
Aydinonat, Denise
Bieber, Claudia
Ruf, Thomas
author_sort Hoelzl, Franz
collection PubMed
description Telomere shortening is thought to be an important biomarker for life history traits such as lifespan and aging, and can be indicative of genome integrity, survival probability and the risk of cancer development. In humans and other animals, telomeres almost always shorten with age, with more rapid telomere attrition in short-lived species. Here, we show that in the edible dormouse (Glis glis) telomere length significantly increases from an age of 6 to an age of 9 years. While this finding could be due to higher survival of individuals with longer telomeres, we also found, using longitudinal measurements, a positive effect of age on the rate of telomere elongation within older individuals. To our knowledge, no previous study has reported such an effect of age on telomere lengthening. We attribute this exceptional pattern to the peculiar life-history of this species, which skips reproduction in years with low food availability. Further, we show that this “sit tight” strategy in the timing of reproduction is associated with an increasing likelihood for an individual to reproduce as it ages. As reproduction could facilitate telomere attrition, this life-history strategy may have led to the evolution of increased somatic maintenance and telomere elongation with increasing age.
format Online
Article
Text
id pubmed-5121655
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-51216552016-11-28 Telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (Glis glis) Hoelzl, Franz Smith, Steve Cornils, Jessica S. Aydinonat, Denise Bieber, Claudia Ruf, Thomas Sci Rep Article Telomere shortening is thought to be an important biomarker for life history traits such as lifespan and aging, and can be indicative of genome integrity, survival probability and the risk of cancer development. In humans and other animals, telomeres almost always shorten with age, with more rapid telomere attrition in short-lived species. Here, we show that in the edible dormouse (Glis glis) telomere length significantly increases from an age of 6 to an age of 9 years. While this finding could be due to higher survival of individuals with longer telomeres, we also found, using longitudinal measurements, a positive effect of age on the rate of telomere elongation within older individuals. To our knowledge, no previous study has reported such an effect of age on telomere lengthening. We attribute this exceptional pattern to the peculiar life-history of this species, which skips reproduction in years with low food availability. Further, we show that this “sit tight” strategy in the timing of reproduction is associated with an increasing likelihood for an individual to reproduce as it ages. As reproduction could facilitate telomere attrition, this life-history strategy may have led to the evolution of increased somatic maintenance and telomere elongation with increasing age. Nature Publishing Group 2016-11-24 /pmc/articles/PMC5121655/ /pubmed/27883035 http://dx.doi.org/10.1038/srep36856 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hoelzl, Franz
Smith, Steve
Cornils, Jessica S.
Aydinonat, Denise
Bieber, Claudia
Ruf, Thomas
Telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (Glis glis)
title Telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (Glis glis)
title_full Telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (Glis glis)
title_fullStr Telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (Glis glis)
title_full_unstemmed Telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (Glis glis)
title_short Telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (Glis glis)
title_sort telomeres are elongated in older individuals in a hibernating rodent, the edible dormouse (glis glis)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121655/
https://www.ncbi.nlm.nih.gov/pubmed/27883035
http://dx.doi.org/10.1038/srep36856
work_keys_str_mv AT hoelzlfranz telomeresareelongatedinolderindividualsinahibernatingrodenttheedibledormouseglisglis
AT smithsteve telomeresareelongatedinolderindividualsinahibernatingrodenttheedibledormouseglisglis
AT cornilsjessicas telomeresareelongatedinolderindividualsinahibernatingrodenttheedibledormouseglisglis
AT aydinonatdenise telomeresareelongatedinolderindividualsinahibernatingrodenttheedibledormouseglisglis
AT bieberclaudia telomeresareelongatedinolderindividualsinahibernatingrodenttheedibledormouseglisglis
AT rufthomas telomeresareelongatedinolderindividualsinahibernatingrodenttheedibledormouseglisglis