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Bi-directional effects of vitamin B(12) and methotrexate on Daphnia magna fitness and genomic methylation
Here we interrogated, using three separate but complementary experimental approaches, the impact of vitamin B(12) availability and methotrexate exposure on Daphnia magna, which we hypothesised should have an opposite effect on One carbon metabolism (OCM). OCM is a vital biological process supporting...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605502/ https://www.ncbi.nlm.nih.gov/pubmed/28928387 http://dx.doi.org/10.1038/s41598-017-12148-2 |
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author | Kusari, Fitore O’Doherty, Alan M. Hodges, Nikolas J. Wojewodzic, Marcin W. |
author_facet | Kusari, Fitore O’Doherty, Alan M. Hodges, Nikolas J. Wojewodzic, Marcin W. |
author_sort | Kusari, Fitore |
collection | PubMed |
description | Here we interrogated, using three separate but complementary experimental approaches, the impact of vitamin B(12) availability and methotrexate exposure on Daphnia magna, which we hypothesised should have an opposite effect on One carbon metabolism (OCM). OCM is a vital biological process supporting a variety of physiological processes, including DNA methylation. Contrary to mammalian models, this process remains largely unexplored in invertebrates. The purpose of this study was to elucidate the impact of OCM short-term alteration on the fitness and epigenome of the keystone species, Daphnia. We used maternal age at reproduction, brood size and survival rates in combination with DNA methylation sensitive comet assay to determine the effects of vitamin B(12) or MTX on fitness and the epigenome. Vitamin B(12) had a positive influence on Daphnia fitness and we provide evidence demonstrating that this may be associated with an increased level of genome-wide DNA methylation. Conversely, exposing D. magna to MTX negatively influenced the fitness of the animals and was associated with loss of global DNA methylation, translating in decreased fitness. These results highlight the potential importance of OCM in invertebrates, providing novel evidence supporting a potential role for epigenetic modifications to the genome in D. magna environmental adaptability. |
format | Online Article Text |
id | pubmed-5605502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56055022017-09-20 Bi-directional effects of vitamin B(12) and methotrexate on Daphnia magna fitness and genomic methylation Kusari, Fitore O’Doherty, Alan M. Hodges, Nikolas J. Wojewodzic, Marcin W. Sci Rep Article Here we interrogated, using three separate but complementary experimental approaches, the impact of vitamin B(12) availability and methotrexate exposure on Daphnia magna, which we hypothesised should have an opposite effect on One carbon metabolism (OCM). OCM is a vital biological process supporting a variety of physiological processes, including DNA methylation. Contrary to mammalian models, this process remains largely unexplored in invertebrates. The purpose of this study was to elucidate the impact of OCM short-term alteration on the fitness and epigenome of the keystone species, Daphnia. We used maternal age at reproduction, brood size and survival rates in combination with DNA methylation sensitive comet assay to determine the effects of vitamin B(12) or MTX on fitness and the epigenome. Vitamin B(12) had a positive influence on Daphnia fitness and we provide evidence demonstrating that this may be associated with an increased level of genome-wide DNA methylation. Conversely, exposing D. magna to MTX negatively influenced the fitness of the animals and was associated with loss of global DNA methylation, translating in decreased fitness. These results highlight the potential importance of OCM in invertebrates, providing novel evidence supporting a potential role for epigenetic modifications to the genome in D. magna environmental adaptability. Nature Publishing Group UK 2017-09-19 /pmc/articles/PMC5605502/ /pubmed/28928387 http://dx.doi.org/10.1038/s41598-017-12148-2 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kusari, Fitore O’Doherty, Alan M. Hodges, Nikolas J. Wojewodzic, Marcin W. Bi-directional effects of vitamin B(12) and methotrexate on Daphnia magna fitness and genomic methylation |
title | Bi-directional effects of vitamin B(12) and methotrexate on Daphnia magna fitness and genomic methylation |
title_full | Bi-directional effects of vitamin B(12) and methotrexate on Daphnia magna fitness and genomic methylation |
title_fullStr | Bi-directional effects of vitamin B(12) and methotrexate on Daphnia magna fitness and genomic methylation |
title_full_unstemmed | Bi-directional effects of vitamin B(12) and methotrexate on Daphnia magna fitness and genomic methylation |
title_short | Bi-directional effects of vitamin B(12) and methotrexate on Daphnia magna fitness and genomic methylation |
title_sort | bi-directional effects of vitamin b(12) and methotrexate on daphnia magna fitness and genomic methylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605502/ https://www.ncbi.nlm.nih.gov/pubmed/28928387 http://dx.doi.org/10.1038/s41598-017-12148-2 |
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