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Thyroid hormone links environmental signals to DNA methylation.
- Source :
-
Philosophical Transactions of the Royal Society B: Biological Sciences . 3/25/2024, Vol. 379 Issue 1898, p1-9. 9p. - Publication Year :
- 2024
-
Abstract
- Environmental conditions experienced within and across generations can impact individual phenotypes via so-called 'epigenetic' processes. Here we suggest that endocrine signalling acts as a 'sensor' linking environmental inputs to epigenetic modifications. We focus on thyroid hormone signalling and DNA methylation, but other mechanisms are likely to act in a similar manner. DNA methylation is one of the most important epigenetic mechanisms, which alters gene expression patterns by methylating cytosine bases via DNA methyltransferase enzymes. Thyroid hormone is mechanistically linked to DNA methylation, at least partly by regulating the activity of DNA methyltransferase 3a, which is the principal enzyme that mediates epigenetic responses to environmental change. Thyroid signalling is sensitive to natural and anthropogenic environmental impacts (e.g. light, temperature, endocrine-disrupting pollution), and here we propose that thyroid hormone acts as an environmental sensor to mediate epigenetic modifications. The nexus between thyroid hormone signalling and DNA methylation can integrate multiple environmental signals to modify phenotypes, and coordinate phenotypic plasticity at different time scales, such as within and across generations. These dynamics can have wide-ranging effects on health and fitness of animals, because they influence the time course of phenotypic adjustments and potentially the range of environmental stimuli that can elicit epigenetic responses. This article is part of the theme issue 'Endocrine responses to environmental variation: conceptual approaches and recent developments'. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 09628436
- Volume :
- 379
- Issue :
- 1898
- Database :
- Academic Search Index
- Journal :
- Philosophical Transactions of the Royal Society B: Biological Sciences
- Publication Type :
- Academic Journal
- Accession number :
- 175237503
- Full Text :
- https://doi.org/10.1098/rstb.2022.0506