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Development of DNA methylation‐based epigenetic age predictors in loblolly pine (Pinus taeda)

Biological ageing is connected to life history variation across ecological scales and informs a basic understanding of age‐related declines in organismal function. Altered DNA methylation dynamics are a conserved aspect of biological ageing and have recently been modelled to predict chronological ag...

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Autores principales: Gardner, Steven T., Bertucci, Emily M., Sutton, Randall, Horcher, Andy, Aubrey, Doug, Parrott, Benjamin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087248/
https://www.ncbi.nlm.nih.gov/pubmed/35957540
http://dx.doi.org/10.1111/1755-0998.13698
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author Gardner, Steven T.
Bertucci, Emily M.
Sutton, Randall
Horcher, Andy
Aubrey, Doug
Parrott, Benjamin B.
author_facet Gardner, Steven T.
Bertucci, Emily M.
Sutton, Randall
Horcher, Andy
Aubrey, Doug
Parrott, Benjamin B.
author_sort Gardner, Steven T.
collection PubMed
description Biological ageing is connected to life history variation across ecological scales and informs a basic understanding of age‐related declines in organismal function. Altered DNA methylation dynamics are a conserved aspect of biological ageing and have recently been modelled to predict chronological age among vertebrate species. In addition to their utility in estimating individual age, differences between chronological and predicted ages arise due to acceleration or deceleration of epigenetic ageing, and these discrepancies are linked to disease risk and multiple life history traits. Although evidence suggests that patterns of DNA methylation can describe ageing in plants, predictions with epigenetic clocks have yet to be performed. Here, we resolve the DNA methylome across CpG, CHG, and CHH‐methylation contexts in the loblolly pine tree (Pinus taeda) and construct epigenetic clocks capable of predicting ages in this species within 6% of its maximum lifespan. Although patterns of CHH‐methylation showed little association with age, both CpG and CHG‐methylation contexts were strongly associated with ageing, largely becoming hypomethylated with age. Among age‐associated loci were those in close proximity to malate dehydrogenase, NADH dehydrogenase, and 18S and 26S ribosomal RNA genes. This study reports one of the first epigenetic clocks in plants and demonstrates the universality of age‐associated DNA methylation dynamics which can inform conservation and management practices, as well as our ecological and evolutionary understanding of biological ageing in plants.
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spelling pubmed-100872482023-04-12 Development of DNA methylation‐based epigenetic age predictors in loblolly pine (Pinus taeda) Gardner, Steven T. Bertucci, Emily M. Sutton, Randall Horcher, Andy Aubrey, Doug Parrott, Benjamin B. Mol Ecol Resour RESOURCE ARTICLES Biological ageing is connected to life history variation across ecological scales and informs a basic understanding of age‐related declines in organismal function. Altered DNA methylation dynamics are a conserved aspect of biological ageing and have recently been modelled to predict chronological age among vertebrate species. In addition to their utility in estimating individual age, differences between chronological and predicted ages arise due to acceleration or deceleration of epigenetic ageing, and these discrepancies are linked to disease risk and multiple life history traits. Although evidence suggests that patterns of DNA methylation can describe ageing in plants, predictions with epigenetic clocks have yet to be performed. Here, we resolve the DNA methylome across CpG, CHG, and CHH‐methylation contexts in the loblolly pine tree (Pinus taeda) and construct epigenetic clocks capable of predicting ages in this species within 6% of its maximum lifespan. Although patterns of CHH‐methylation showed little association with age, both CpG and CHG‐methylation contexts were strongly associated with ageing, largely becoming hypomethylated with age. Among age‐associated loci were those in close proximity to malate dehydrogenase, NADH dehydrogenase, and 18S and 26S ribosomal RNA genes. This study reports one of the first epigenetic clocks in plants and demonstrates the universality of age‐associated DNA methylation dynamics which can inform conservation and management practices, as well as our ecological and evolutionary understanding of biological ageing in plants. John Wiley and Sons Inc. 2022-08-24 2023-01 /pmc/articles/PMC10087248/ /pubmed/35957540 http://dx.doi.org/10.1111/1755-0998.13698 Text en © 2022 The Authors. Molecular Ecology Resources published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle RESOURCE ARTICLES
Gardner, Steven T.
Bertucci, Emily M.
Sutton, Randall
Horcher, Andy
Aubrey, Doug
Parrott, Benjamin B.
Development of DNA methylation‐based epigenetic age predictors in loblolly pine (Pinus taeda)
title Development of DNA methylation‐based epigenetic age predictors in loblolly pine (Pinus taeda)
title_full Development of DNA methylation‐based epigenetic age predictors in loblolly pine (Pinus taeda)
title_fullStr Development of DNA methylation‐based epigenetic age predictors in loblolly pine (Pinus taeda)
title_full_unstemmed Development of DNA methylation‐based epigenetic age predictors in loblolly pine (Pinus taeda)
title_short Development of DNA methylation‐based epigenetic age predictors in loblolly pine (Pinus taeda)
title_sort development of dna methylation‐based epigenetic age predictors in loblolly pine (pinus taeda)
topic RESOURCE ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087248/
https://www.ncbi.nlm.nih.gov/pubmed/35957540
http://dx.doi.org/10.1111/1755-0998.13698
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