DNA methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird

© 2017 De Paoli-Iseppi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Most seabirds do not have any outw...

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Main Authors: De Paoli-Iseppi, R., Polanowski, A., McMahon, C., Deagle, B., Dickinson, J., Hindell, M., Jarman, Simon
Format: Journal Article
Published: Public Library of Science 2017
Online Access:http://hdl.handle.net/20.500.11937/73205
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author De Paoli-Iseppi, R.
Polanowski, A.
McMahon, C.
Deagle, B.
Dickinson, J.
Hindell, M.
Jarman, Simon
author_facet De Paoli-Iseppi, R.
Polanowski, A.
McMahon, C.
Deagle, B.
Dickinson, J.
Hindell, M.
Jarman, Simon
author_sort De Paoli-Iseppi, R.
building Curtin Institutional Repository
collection Online Access
description © 2017 De Paoli-Iseppi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Most seabirds do not have any outward identifiers of their chronological age, so estimation of seabird population age structure generally requires expensive, long-term banding studies. We investigated the potential to use a molecular age biomarker to estimate age in short-tailed shearwaters (Ardenna tenuirostris). We quantified DNA methylation in several A. tenuirostris genes that have shown age-related methylation changes in mammals. In birds ranging from chicks to 21 years of age, bisulphite treated blood and feather DNA was sequenced and methylation levels analysed in 67 CpG sites in 13 target gene regions. From blood samples, five of the top relationships with age were identified in KCNC3 loci (CpG66: R2 = 0.325, p = 0.019). In feather samples ELOVL2 (CpG42: R2 = 0.285, p = 0.00048) and EDARADD (CpG46: R2 = 0.168, p = 0.0067) were also weakly correlated with age. However, the majority of markers had no clear association with age (of 131 comparisons only 12 had a p-value < 0.05) and statistical analysis using a penalised lasso approach did not produce an accurate ageing model. Our data indicate that some age-related signatures identified in orthologous mammalian genes are not conserved in the long-lived short tailed shearwater. Alternative molecular approaches will be required to identify a reliable biomarker of chronological age in these seabirds.
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spelling curtin-20.500.11937-732052019-03-20T04:05:07Z DNA methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird De Paoli-Iseppi, R. Polanowski, A. McMahon, C. Deagle, B. Dickinson, J. Hindell, M. Jarman, Simon © 2017 De Paoli-Iseppi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Most seabirds do not have any outward identifiers of their chronological age, so estimation of seabird population age structure generally requires expensive, long-term banding studies. We investigated the potential to use a molecular age biomarker to estimate age in short-tailed shearwaters (Ardenna tenuirostris). We quantified DNA methylation in several A. tenuirostris genes that have shown age-related methylation changes in mammals. In birds ranging from chicks to 21 years of age, bisulphite treated blood and feather DNA was sequenced and methylation levels analysed in 67 CpG sites in 13 target gene regions. From blood samples, five of the top relationships with age were identified in KCNC3 loci (CpG66: R2 = 0.325, p = 0.019). In feather samples ELOVL2 (CpG42: R2 = 0.285, p = 0.00048) and EDARADD (CpG46: R2 = 0.168, p = 0.0067) were also weakly correlated with age. However, the majority of markers had no clear association with age (of 131 comparisons only 12 had a p-value < 0.05) and statistical analysis using a penalised lasso approach did not produce an accurate ageing model. Our data indicate that some age-related signatures identified in orthologous mammalian genes are not conserved in the long-lived short tailed shearwater. Alternative molecular approaches will be required to identify a reliable biomarker of chronological age in these seabirds. 2017 Journal Article http://hdl.handle.net/20.500.11937/73205 10.1371/journal.pone.0189181 http://creativecommons.org/licenses/by/4.0/ Public Library of Science fulltext
spellingShingle De Paoli-Iseppi, R.
Polanowski, A.
McMahon, C.
Deagle, B.
Dickinson, J.
Hindell, M.
Jarman, Simon
DNA methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird
title DNA methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird
title_full DNA methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird
title_fullStr DNA methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird
title_full_unstemmed DNA methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird
title_short DNA methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird
title_sort dna methylation levels in candidate genes associated with chronological age in mammals are not conserved in a long-lived seabird
url http://hdl.handle.net/20.500.11937/73205