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Does Arsenic Contamination Affect DNA Methylation Patterns in a Wild Bird Population? An Experimental Approach
[Image: see text] Pollutants, such as toxic metals, negatively influence organismal health and performance, even leading to population collapses. Studies in model organisms have shown that epigenetic marks, such as DNA methylation, can be modulated by various environmental factors, including polluta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277128/ https://www.ncbi.nlm.nih.gov/pubmed/34110128 http://dx.doi.org/10.1021/acs.est.0c08621 |
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author | Laine, Veronika N. Verschuuren, Mark van Oers, Kees Espín, Silvia Sánchez-Virosta, Pablo Eeva, Tapio Ruuskanen, Suvi |
author_facet | Laine, Veronika N. Verschuuren, Mark van Oers, Kees Espín, Silvia Sánchez-Virosta, Pablo Eeva, Tapio Ruuskanen, Suvi |
author_sort | Laine, Veronika N. |
collection | PubMed |
description | [Image: see text] Pollutants, such as toxic metals, negatively influence organismal health and performance, even leading to population collapses. Studies in model organisms have shown that epigenetic marks, such as DNA methylation, can be modulated by various environmental factors, including pollutants, influencing gene expression, and various organismal traits. Yet experimental data on the effects of pollution on DNA methylation from wild animal populations are largely lacking. We here experimentally investigated for the first time the effects of early-life exposure to environmentally relevant levels of a key pollutant, arsenic (As), on genome-wide DNA methylation in a wild bird population. We experimentally exposed nestlings of great tits (Parus major) to arsenic during their postnatal developmental period (3 to 14 days post-hatching) and compared their erythrocyte DNA methylation levels to those of respective controls. In contrast to predictions, we found no overall hypomethylation in the arsenic group. We found evidence for loci to be differentially methylated between the treatment groups, but for five CpG sites only. Three of the sites were located in gene bodies of zinc finger and BTB domain containing 47 (ZBTB47), HIVEP zinc finger 3 (HIVEP3), and insulin-like growth factor 2 mRNA binding protein 1 (IGF2BP1). Further studies are needed to evaluate whether epigenetic dysregulation is a commonly observed phenomenon in polluted populations and what are the consequences for organism functioning and for population dynamics. |
format | Online Article Text |
id | pubmed-8277128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82771282021-07-14 Does Arsenic Contamination Affect DNA Methylation Patterns in a Wild Bird Population? An Experimental Approach Laine, Veronika N. Verschuuren, Mark van Oers, Kees Espín, Silvia Sánchez-Virosta, Pablo Eeva, Tapio Ruuskanen, Suvi Environ Sci Technol [Image: see text] Pollutants, such as toxic metals, negatively influence organismal health and performance, even leading to population collapses. Studies in model organisms have shown that epigenetic marks, such as DNA methylation, can be modulated by various environmental factors, including pollutants, influencing gene expression, and various organismal traits. Yet experimental data on the effects of pollution on DNA methylation from wild animal populations are largely lacking. We here experimentally investigated for the first time the effects of early-life exposure to environmentally relevant levels of a key pollutant, arsenic (As), on genome-wide DNA methylation in a wild bird population. We experimentally exposed nestlings of great tits (Parus major) to arsenic during their postnatal developmental period (3 to 14 days post-hatching) and compared their erythrocyte DNA methylation levels to those of respective controls. In contrast to predictions, we found no overall hypomethylation in the arsenic group. We found evidence for loci to be differentially methylated between the treatment groups, but for five CpG sites only. Three of the sites were located in gene bodies of zinc finger and BTB domain containing 47 (ZBTB47), HIVEP zinc finger 3 (HIVEP3), and insulin-like growth factor 2 mRNA binding protein 1 (IGF2BP1). Further studies are needed to evaluate whether epigenetic dysregulation is a commonly observed phenomenon in polluted populations and what are the consequences for organism functioning and for population dynamics. American Chemical Society 2021-06-10 2021-07-06 /pmc/articles/PMC8277128/ /pubmed/34110128 http://dx.doi.org/10.1021/acs.est.0c08621 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Laine, Veronika N. Verschuuren, Mark van Oers, Kees Espín, Silvia Sánchez-Virosta, Pablo Eeva, Tapio Ruuskanen, Suvi Does Arsenic Contamination Affect DNA Methylation Patterns in a Wild Bird Population? An Experimental Approach |
title | Does
Arsenic Contamination Affect DNA Methylation
Patterns in a Wild Bird Population? An Experimental Approach |
title_full | Does
Arsenic Contamination Affect DNA Methylation
Patterns in a Wild Bird Population? An Experimental Approach |
title_fullStr | Does
Arsenic Contamination Affect DNA Methylation
Patterns in a Wild Bird Population? An Experimental Approach |
title_full_unstemmed | Does
Arsenic Contamination Affect DNA Methylation
Patterns in a Wild Bird Population? An Experimental Approach |
title_short | Does
Arsenic Contamination Affect DNA Methylation
Patterns in a Wild Bird Population? An Experimental Approach |
title_sort | does
arsenic contamination affect dna methylation
patterns in a wild bird population? an experimental approach |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277128/ https://www.ncbi.nlm.nih.gov/pubmed/34110128 http://dx.doi.org/10.1021/acs.est.0c08621 |
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