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Embryonic and postnatal telomere length decrease with ovulation order within clutches

Telomere length (TL) in early life has been found to be predictive of subsequent lifespan. Factors such as parental TL, parental age and environmental conditions during development have been shown to contribute to the observed variation in TL among individuals. One factor that has not hitherto been...

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Autores principales: Noguera, José C., Metcalfe, Neil B., Reichert, Sophie, Monaghan, Pat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865837/
https://www.ncbi.nlm.nih.gov/pubmed/27174767
http://dx.doi.org/10.1038/srep25915
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author Noguera, José C.
Metcalfe, Neil B.
Reichert, Sophie
Monaghan, Pat
author_facet Noguera, José C.
Metcalfe, Neil B.
Reichert, Sophie
Monaghan, Pat
author_sort Noguera, José C.
collection PubMed
description Telomere length (TL) in early life has been found to be predictive of subsequent lifespan. Factors such as parental TL, parental age and environmental conditions during development have been shown to contribute to the observed variation in TL among individuals. One factor that has not hitherto been considered is ovulation order, although it is well established that the last hatched/born offspring in a brood or litter often show relatively poor subsequent performance. We examined the within- and across-clutch effect of ovulation order on TL in embryos of zebra finches experiencing the same controlled incubation conditions (N = 151), and tested whether any such ovulation order effects remained detectable in adults (N = 122). Irrespective of clutch and egg size, TL in early-stage embryos (72 h incubation) markedly decreased with within-clutch ovulation order; the difference in TL of first and last-laid embryos was equivalent to the average within-individual telomere loss over the entire period of nestling and juvenile life. This ovulation-order effect occurred only within but not across clutches, and was still evident in adults. Given that TL in early life predicts lifespan, our results suggest that parental effects on telomere length could contribute to the known poor performance of later-ovulated family members.
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spelling pubmed-48658372016-05-23 Embryonic and postnatal telomere length decrease with ovulation order within clutches Noguera, José C. Metcalfe, Neil B. Reichert, Sophie Monaghan, Pat Sci Rep Article Telomere length (TL) in early life has been found to be predictive of subsequent lifespan. Factors such as parental TL, parental age and environmental conditions during development have been shown to contribute to the observed variation in TL among individuals. One factor that has not hitherto been considered is ovulation order, although it is well established that the last hatched/born offspring in a brood or litter often show relatively poor subsequent performance. We examined the within- and across-clutch effect of ovulation order on TL in embryos of zebra finches experiencing the same controlled incubation conditions (N = 151), and tested whether any such ovulation order effects remained detectable in adults (N = 122). Irrespective of clutch and egg size, TL in early-stage embryos (72 h incubation) markedly decreased with within-clutch ovulation order; the difference in TL of first and last-laid embryos was equivalent to the average within-individual telomere loss over the entire period of nestling and juvenile life. This ovulation-order effect occurred only within but not across clutches, and was still evident in adults. Given that TL in early life predicts lifespan, our results suggest that parental effects on telomere length could contribute to the known poor performance of later-ovulated family members. Nature Publishing Group 2016-05-13 /pmc/articles/PMC4865837/ /pubmed/27174767 http://dx.doi.org/10.1038/srep25915 Text en Copyright © 2016, Macmillan Publishers Limited 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
Noguera, José C.
Metcalfe, Neil B.
Reichert, Sophie
Monaghan, Pat
Embryonic and postnatal telomere length decrease with ovulation order within clutches
title Embryonic and postnatal telomere length decrease with ovulation order within clutches
title_full Embryonic and postnatal telomere length decrease with ovulation order within clutches
title_fullStr Embryonic and postnatal telomere length decrease with ovulation order within clutches
title_full_unstemmed Embryonic and postnatal telomere length decrease with ovulation order within clutches
title_short Embryonic and postnatal telomere length decrease with ovulation order within clutches
title_sort embryonic and postnatal telomere length decrease with ovulation order within clutches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865837/
https://www.ncbi.nlm.nih.gov/pubmed/27174767
http://dx.doi.org/10.1038/srep25915
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