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Telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not

Attempts to understand the causes of variation in senescence trajectories would benefit greatly from biomarkers that reflect the progressive declines in somatic integrity (SI) that lead to senescence. While telomere length has attracted considerable interest in this regard, sources of variation in t...

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Autores principales: Wood, Emma M., Young, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6772082/
https://www.ncbi.nlm.nih.gov/pubmed/31332860
http://dx.doi.org/10.1111/mec.15181
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author Wood, Emma M.
Young, Andrew J.
author_facet Wood, Emma M.
Young, Andrew J.
author_sort Wood, Emma M.
collection PubMed
description Attempts to understand the causes of variation in senescence trajectories would benefit greatly from biomarkers that reflect the progressive declines in somatic integrity (SI) that lead to senescence. While telomere length has attracted considerable interest in this regard, sources of variation in telomere length potentially unrelated to declines in SI could, in some contexts, leave telomere attrition rates a more effective biomarker than telomere length alone. Here, we investigate whether telomere length and telomere attrition rates predict the survival of wild white‐browed sparrow‐weaver nestlings (Plocepasser mahali). Our analyses of telomere length reveal counterintuitive patterns: telomere length soon after hatching negatively predicted nestling survival to fledging, a pattern that appears to be driven by differentially high in‐nest predation of broods with longer telomeres. Telomere length did not predict survival outside this period: neither hatchling telomere length nor telomere length in the mid‐nestling period predicted survival from fledging to adulthood. Our analyses using within‐individual telomere attrition rates, by contrast, revealed the expected relationships: nestlings that experienced a higher rate of telomere attrition were less likely to survive to adulthood, regardless of their initial telomere length and independent of effects of body mass. Our findings support the growing use of telomeric traits as biomarkers of SI, but lend strength to the view that longitudinal assessments of within‐individual telomere attrition since early life may be a more effective biomarker in some contexts than telomere length alone.
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spelling pubmed-67720822019-10-07 Telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not Wood, Emma M. Young, Andrew J. Mol Ecol ORIGINAL ARTICLES Attempts to understand the causes of variation in senescence trajectories would benefit greatly from biomarkers that reflect the progressive declines in somatic integrity (SI) that lead to senescence. While telomere length has attracted considerable interest in this regard, sources of variation in telomere length potentially unrelated to declines in SI could, in some contexts, leave telomere attrition rates a more effective biomarker than telomere length alone. Here, we investigate whether telomere length and telomere attrition rates predict the survival of wild white‐browed sparrow‐weaver nestlings (Plocepasser mahali). Our analyses of telomere length reveal counterintuitive patterns: telomere length soon after hatching negatively predicted nestling survival to fledging, a pattern that appears to be driven by differentially high in‐nest predation of broods with longer telomeres. Telomere length did not predict survival outside this period: neither hatchling telomere length nor telomere length in the mid‐nestling period predicted survival from fledging to adulthood. Our analyses using within‐individual telomere attrition rates, by contrast, revealed the expected relationships: nestlings that experienced a higher rate of telomere attrition were less likely to survive to adulthood, regardless of their initial telomere length and independent of effects of body mass. Our findings support the growing use of telomeric traits as biomarkers of SI, but lend strength to the view that longitudinal assessments of within‐individual telomere attrition since early life may be a more effective biomarker in some contexts than telomere length alone. John Wiley and Sons Inc. 2019-08-07 2019-08 /pmc/articles/PMC6772082/ /pubmed/31332860 http://dx.doi.org/10.1111/mec.15181 Text en © 2019 The Authors.Molecular Ecology Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle ORIGINAL ARTICLES
Wood, Emma M.
Young, Andrew J.
Telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not
title Telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not
title_full Telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not
title_fullStr Telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not
title_full_unstemmed Telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not
title_short Telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not
title_sort telomere attrition predicts reduced survival in a wild social bird, but short telomeres do not
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6772082/
https://www.ncbi.nlm.nih.gov/pubmed/31332860
http://dx.doi.org/10.1111/mec.15181
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