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Transcriptional analysis of the response of C. elegans to ethanol exposure
Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a timecourse of ethanol exposure, between 30 min and 8 h, to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155136/ https://www.ncbi.nlm.nih.gov/pubmed/34040055 http://dx.doi.org/10.1038/s41598-021-90282-8 |
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author | Sterken, Mark G. van Wijk, Marijke H. Quamme, Elizabeth C. Riksen, Joost A. G. Carnell, Lucinda Mathies, Laura D. Davies, Andrew G. Kammenga, Jan E. Bettinger, Jill C. |
author_facet | Sterken, Mark G. van Wijk, Marijke H. Quamme, Elizabeth C. Riksen, Joost A. G. Carnell, Lucinda Mathies, Laura D. Davies, Andrew G. Kammenga, Jan E. Bettinger, Jill C. |
author_sort | Sterken, Mark G. |
collection | PubMed |
description | Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a timecourse of ethanol exposure, between 30 min and 8 h, to determine what genes and genetic pathways are regulated in response to ethanol in this model. We found that short exposures to ethanol (up to 2 h) induced expression of metabolic enzymes involved in metabolizing ethanol and retinol, while longer exposure (8 h) had much more profound effects on the transcriptome. Several genes that are known to be involved in the physiological response to ethanol, including direct ethanol targets, were regulated at 8 h of exposure. This longer exposure to ethanol also resulted in the regulation of genes involved in cilia function, which is consistent with an important role for the effects of ethanol on cilia in the deleterious effects of chronic ethanol consumption in humans. Finally, we found that food deprivation for an 8-h period induced gene expression changes that were somewhat ameliorated by the presence of ethanol, supporting previous observations that worms can use ethanol as a calorie source. |
format | Online Article Text |
id | pubmed-8155136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81551362021-05-27 Transcriptional analysis of the response of C. elegans to ethanol exposure Sterken, Mark G. van Wijk, Marijke H. Quamme, Elizabeth C. Riksen, Joost A. G. Carnell, Lucinda Mathies, Laura D. Davies, Andrew G. Kammenga, Jan E. Bettinger, Jill C. Sci Rep Article Ethanol-induced transcriptional changes underlie important physiological responses to ethanol that are likely to contribute to the addictive properties of the drug. We examined the transcriptional responses of Caenorhabditis elegans across a timecourse of ethanol exposure, between 30 min and 8 h, to determine what genes and genetic pathways are regulated in response to ethanol in this model. We found that short exposures to ethanol (up to 2 h) induced expression of metabolic enzymes involved in metabolizing ethanol and retinol, while longer exposure (8 h) had much more profound effects on the transcriptome. Several genes that are known to be involved in the physiological response to ethanol, including direct ethanol targets, were regulated at 8 h of exposure. This longer exposure to ethanol also resulted in the regulation of genes involved in cilia function, which is consistent with an important role for the effects of ethanol on cilia in the deleterious effects of chronic ethanol consumption in humans. Finally, we found that food deprivation for an 8-h period induced gene expression changes that were somewhat ameliorated by the presence of ethanol, supporting previous observations that worms can use ethanol as a calorie source. Nature Publishing Group UK 2021-05-26 /pmc/articles/PMC8155136/ /pubmed/34040055 http://dx.doi.org/10.1038/s41598-021-90282-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sterken, Mark G. van Wijk, Marijke H. Quamme, Elizabeth C. Riksen, Joost A. G. Carnell, Lucinda Mathies, Laura D. Davies, Andrew G. Kammenga, Jan E. Bettinger, Jill C. Transcriptional analysis of the response of C. elegans to ethanol exposure |
title | Transcriptional analysis of the response of C. elegans to ethanol exposure |
title_full | Transcriptional analysis of the response of C. elegans to ethanol exposure |
title_fullStr | Transcriptional analysis of the response of C. elegans to ethanol exposure |
title_full_unstemmed | Transcriptional analysis of the response of C. elegans to ethanol exposure |
title_short | Transcriptional analysis of the response of C. elegans to ethanol exposure |
title_sort | transcriptional analysis of the response of c. elegans to ethanol exposure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155136/ https://www.ncbi.nlm.nih.gov/pubmed/34040055 http://dx.doi.org/10.1038/s41598-021-90282-8 |
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