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DNA methylation signatures of early life adversity are exposure-dependent in wild baboons

The early life environment can profoundly shape the trajectory of an animal’s life, even years or decades later. One mechanism proposed to contribute to these early life effects is DNA methylation. However, the frequency and functional importance of DNA methylation in shaping early life effects on a...

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Autores principales: Anderson, Jordan A., Lin, Dana, Lea, Amanda J., Johnston, Rachel A., Voyles, Tawni, Akinyi, Mercy Y., Archie, Elizabeth A., Alberts, Susan C., Tung, Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274726/
https://www.ncbi.nlm.nih.gov/pubmed/37333311
http://dx.doi.org/10.1101/2023.06.05.542485
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author Anderson, Jordan A.
Lin, Dana
Lea, Amanda J.
Johnston, Rachel A.
Voyles, Tawni
Akinyi, Mercy Y.
Archie, Elizabeth A.
Alberts, Susan C.
Tung, Jenny
author_facet Anderson, Jordan A.
Lin, Dana
Lea, Amanda J.
Johnston, Rachel A.
Voyles, Tawni
Akinyi, Mercy Y.
Archie, Elizabeth A.
Alberts, Susan C.
Tung, Jenny
author_sort Anderson, Jordan A.
collection PubMed
description The early life environment can profoundly shape the trajectory of an animal’s life, even years or decades later. One mechanism proposed to contribute to these early life effects is DNA methylation. However, the frequency and functional importance of DNA methylation in shaping early life effects on adult outcomes is poorly understood, especially in natural populations. Here, we integrate prospectively collected data on fitness-associated variation in the early environment with DNA methylation estimates at 477,270 CpG sites in 256 wild baboons. We find highly heterogeneous relationships between the early life environment and DNA methylation in adulthood: aspects of the environment linked to resource limitation (e.g., low-quality habitat, early life drought) are associated with many more CpG sites than other types of environmental stressors (e.g., low maternal social status). Sites associated with early resource limitation are enriched in gene bodies and putative enhancers, suggesting they are functionally relevant. Indeed, by deploying a baboon-specific, massively parallel reporter assay, we show that a subset of windows containing these sites are capable of regulatory activity, and that, for 88% of early drought-associated sites in these regulatory windows, enhancer activity is DNA methylation-dependent. Together, our results support the idea that DNA methylation patterns contain a persistent signature of the early life environment. However, they also indicate that not all environmental exposures leave an equivalent mark and suggest that socioenvironmental variation at the time of sampling is more likely to be functionally important. Thus, multiple mechanisms must converge to explain early life effects on fitness-related traits.
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spelling pubmed-102747262023-06-17 DNA methylation signatures of early life adversity are exposure-dependent in wild baboons Anderson, Jordan A. Lin, Dana Lea, Amanda J. Johnston, Rachel A. Voyles, Tawni Akinyi, Mercy Y. Archie, Elizabeth A. Alberts, Susan C. Tung, Jenny bioRxiv Article The early life environment can profoundly shape the trajectory of an animal’s life, even years or decades later. One mechanism proposed to contribute to these early life effects is DNA methylation. However, the frequency and functional importance of DNA methylation in shaping early life effects on adult outcomes is poorly understood, especially in natural populations. Here, we integrate prospectively collected data on fitness-associated variation in the early environment with DNA methylation estimates at 477,270 CpG sites in 256 wild baboons. We find highly heterogeneous relationships between the early life environment and DNA methylation in adulthood: aspects of the environment linked to resource limitation (e.g., low-quality habitat, early life drought) are associated with many more CpG sites than other types of environmental stressors (e.g., low maternal social status). Sites associated with early resource limitation are enriched in gene bodies and putative enhancers, suggesting they are functionally relevant. Indeed, by deploying a baboon-specific, massively parallel reporter assay, we show that a subset of windows containing these sites are capable of regulatory activity, and that, for 88% of early drought-associated sites in these regulatory windows, enhancer activity is DNA methylation-dependent. Together, our results support the idea that DNA methylation patterns contain a persistent signature of the early life environment. However, they also indicate that not all environmental exposures leave an equivalent mark and suggest that socioenvironmental variation at the time of sampling is more likely to be functionally important. Thus, multiple mechanisms must converge to explain early life effects on fitness-related traits. Cold Spring Harbor Laboratory 2023-06-05 /pmc/articles/PMC10274726/ /pubmed/37333311 http://dx.doi.org/10.1101/2023.06.05.542485 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Anderson, Jordan A.
Lin, Dana
Lea, Amanda J.
Johnston, Rachel A.
Voyles, Tawni
Akinyi, Mercy Y.
Archie, Elizabeth A.
Alberts, Susan C.
Tung, Jenny
DNA methylation signatures of early life adversity are exposure-dependent in wild baboons
title DNA methylation signatures of early life adversity are exposure-dependent in wild baboons
title_full DNA methylation signatures of early life adversity are exposure-dependent in wild baboons
title_fullStr DNA methylation signatures of early life adversity are exposure-dependent in wild baboons
title_full_unstemmed DNA methylation signatures of early life adversity are exposure-dependent in wild baboons
title_short DNA methylation signatures of early life adversity are exposure-dependent in wild baboons
title_sort dna methylation signatures of early life adversity are exposure-dependent in wild baboons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274726/
https://www.ncbi.nlm.nih.gov/pubmed/37333311
http://dx.doi.org/10.1101/2023.06.05.542485
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