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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...

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Autores principales: Secco, David, Wang, Chuang, Shou, Huixia, Schultz, Matthew D, Chiarenza, Serge, Nussaume, Laurent, Ecker, Joseph R, Whelan, James, Lister, Ryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
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
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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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