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Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements
Cytosine DNA methylation (mC) is a genome modification that can regulate the expression of coding and non-coding genetic elements. However, little is known about the involvement of mC in response to environmental cues. Using whole genome bisulfite sequencing to assess the spatio-temporal dynamics of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534844/ https://www.ncbi.nlm.nih.gov/pubmed/26196146 http://dx.doi.org/10.7554/eLife.09343 |
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author | Secco, David Wang, Chuang Shou, Huixia Schultz, Matthew D Chiarenza, Serge Nussaume, Laurent Ecker, Joseph R Whelan, James Lister, Ryan |
author_facet | Secco, David Wang, Chuang Shou, Huixia Schultz, Matthew D Chiarenza, Serge Nussaume, Laurent Ecker, Joseph R Whelan, James Lister, Ryan |
author_sort | Secco, David |
collection | PubMed |
description | Cytosine DNA methylation (mC) is a genome modification that can regulate the expression of coding and non-coding genetic elements. However, little is known about the involvement of mC in response to environmental cues. Using whole genome bisulfite sequencing to assess the spatio-temporal dynamics of mC in rice grown under phosphate starvation and recovery conditions, we identified widespread phosphate starvation-induced changes in mC, preferentially localized in transposable elements (TEs) close to highly induced genes. These changes in mC occurred after changes in nearby gene transcription, were mostly DCL3a-independent, and could partially be propagated through mitosis, however no evidence of meiotic transmission was observed. Similar analyses performed in Arabidopsis revealed a very limited effect of phosphate starvation on mC, suggesting a species-specific mechanism. Overall, this suggests that TEs in proximity to environmentally induced genes are silenced via hypermethylation, and establishes the temporal hierarchy of transcriptional and epigenomic changes in response to stress. DOI: http://dx.doi.org/10.7554/eLife.09343.001 |
format | Online Article Text |
id | pubmed-4534844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45348442015-08-13 Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements Secco, David Wang, Chuang Shou, Huixia Schultz, Matthew D Chiarenza, Serge Nussaume, Laurent Ecker, Joseph R Whelan, James Lister, Ryan eLife Genomics and Evolutionary Biology Cytosine DNA methylation (mC) is a genome modification that can regulate the expression of coding and non-coding genetic elements. However, little is known about the involvement of mC in response to environmental cues. Using whole genome bisulfite sequencing to assess the spatio-temporal dynamics of mC in rice grown under phosphate starvation and recovery conditions, we identified widespread phosphate starvation-induced changes in mC, preferentially localized in transposable elements (TEs) close to highly induced genes. These changes in mC occurred after changes in nearby gene transcription, were mostly DCL3a-independent, and could partially be propagated through mitosis, however no evidence of meiotic transmission was observed. Similar analyses performed in Arabidopsis revealed a very limited effect of phosphate starvation on mC, suggesting a species-specific mechanism. Overall, this suggests that TEs in proximity to environmentally induced genes are silenced via hypermethylation, and establishes the temporal hierarchy of transcriptional and epigenomic changes in response to stress. DOI: http://dx.doi.org/10.7554/eLife.09343.001 eLife Sciences Publications, Ltd 2015-07-21 /pmc/articles/PMC4534844/ /pubmed/26196146 http://dx.doi.org/10.7554/eLife.09343 Text en © 2015, Secco et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genomics and Evolutionary Biology Secco, David Wang, Chuang Shou, Huixia Schultz, Matthew D Chiarenza, Serge Nussaume, Laurent Ecker, Joseph R Whelan, James Lister, Ryan Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements |
title | Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements |
title_full | Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements |
title_fullStr | Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements |
title_full_unstemmed | Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements |
title_short | Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements |
title_sort | stress induced gene expression drives transient dna methylation changes at adjacent repetitive elements |
topic | Genomics and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534844/ https://www.ncbi.nlm.nih.gov/pubmed/26196146 http://dx.doi.org/10.7554/eLife.09343 |
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