Abstract
The hypothalamic–pituitary–adrenal (HPA) axis coordinates an organism's response to environmental stress. The responsiveness and sensitivity of an offspring's stress response may be shaped not only by stressors encountered in their early post-natal environment but also by stressors in their parent's environment. Yet, few studies have considered how stressors encountered in both of these early life environments may function together to impact the developing HPA axis. Here, we manipulated stressors in the parental and post-natal environments in a population of house sparrows (Passer domesticus) to assess their impact on changes in DNA methylation (and corresponding gene expression) in a suite of genes within the HPA axis. We found that nestlings that experienced early life stress across both life-history periods had higher DNA methylation in a critical HPA axis gene, the glucocorticoid receptor (NR3C1). In addition, we found that the life-history stage when stress was encountered impacted some genes (HSD11B1, NR3C1 and NR3C2) differently. We also found evidence for the mitigation of parental stress by post-natal stress (in HSD11B1 and NR3C2). Finally, by assessing DNA methylation in both the brain and blood, we were able to evaluate cross-tissue patterns. While some differentially methylated regions were tissue-specific, we found cross-tissue changes in NR3C2 and NR3C1, suggesting that blood is a suitable tissue for assessing DNA methylation as a biomarker of early life stress. Our results provide a crucial first step in understanding the mechanisms by which early life stress in different life-history periods contributes to changes in the epigenome of the HPA axis.
| Original language | English |
|---|---|
| Article number | e17291 |
| Journal | Molecular Ecology |
| Volume | 33 |
| Issue number | 6 |
| DOIs | |
| State | Published - Mar 2024 |
Bibliographical note
Publisher Copyright:© 2024 John Wiley & Sons Ltd.
Funding
We thank the Heidinger and Westneat laboratory members for their assistance in the field and with data collection for this project, especially RC Young, AE Sirman and J Vangorder‐Braid. This work was supported by the US National Science Foundation (DGE‐16‐44869 to S.J.S.W.; IOS‐1257530 and IOS‐1656098 to D.R.R.; IOS‐1257718 to D.F.W.; and IOS‐1656194 to B.J.H.). This study was performed under the approval of North Dakota State University IACUC (protocol A17035). Finally, we thank two anonymous reviewers for useful suggestions that improved the manuscript. This work was supported by the US National Science Foundation (DGE‐16‐44869 to S.J.S.W.; IOS‐1257530 and IOS‐1656098 to D.R.R.; IOS‐1257718 to D.F.W.; and IOS‐1656194 to B.J.H.). We thank the Heidinger and Westneat laboratory members for their assistance in the field and with data collection for this project, especially RC Young, AE Sirman and J Vangorder-Braid. This work was supported by the US National Science Foundation (DGE-16-44869 to S.J.S.W.; IOS-1257530 and IOS-1656098 to D.R.R.; IOS-1257718 to D.F.W.; and IOS-1656194 to B.J.H.). This study was performed under the approval of North Dakota State University IACUC (protocol A17035). Finally, we thank two anonymous reviewers for useful suggestions that improved the manuscript.
| Funders | Funder number |
|---|---|
| National Science Foundation Arctic Social Science Program | IOS‐1656194, IOS‐1257530, IOS‐1656098, DGE‐16‐44869, IOS‐1257718 |
| North Dakota State University | A17035 |
Keywords
- DNA methylation
- HPA axis
- biomarker
- parental effects
- stress
ASJC Scopus subject areas
- Ecology, Evolution, Behavior and Systematics
- Genetics
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