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Post-transcriptional gene silencing triggers dispensable DNA methylation in gene body in Arabidopsis
Spontaneous post-transcriptional silencing of sense transgenes (S-PTGS) is established in each generation and is accompanied by DNA methylation, but the pathway of PTGS-dependent DNA methylation is unknown and so is its role. Here we show that CHH and CHG methylation coincides spatially and temporal...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753489/ https://www.ncbi.nlm.nih.gov/pubmed/31372641 http://dx.doi.org/10.1093/nar/gkz636 |
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author | Taochy, Christelle Yu, Agnès Bouché, Nicolas Bouteiller, Nathalie Elmayan, Taline Dressel, Uwe Carroll, Bernard J Vaucheret, Hervé |
author_facet | Taochy, Christelle Yu, Agnès Bouché, Nicolas Bouteiller, Nathalie Elmayan, Taline Dressel, Uwe Carroll, Bernard J Vaucheret, Hervé |
author_sort | Taochy, Christelle |
collection | PubMed |
description | Spontaneous post-transcriptional silencing of sense transgenes (S-PTGS) is established in each generation and is accompanied by DNA methylation, but the pathway of PTGS-dependent DNA methylation is unknown and so is its role. Here we show that CHH and CHG methylation coincides spatially and temporally with RDR6-dependent products derived from the central and 3′ regions of the coding sequence, and requires the components of the RNA-directed DNA methylation (RdDM) pathway NRPE1, DRD1 and DRM2, but not CLSY1, NRPD1, RDR2 or DCL3, suggesting that RDR6-dependent products, namely long dsRNAs and/or siRNAs, trigger PTGS-dependent DNA methylation. Nevertheless, none of these RdDM components are required to establish S-PTGS or produce a systemic silencing signal. Moreover, preventing de novo DNA methylation in non-silenced transgenic tissues grafted onto homologous silenced tissues does not inhibit the triggering of PTGS. Overall, these data indicate that gene body DNA methylation is a consequence, not a cause, of PTGS, and rule out the hypothesis that a PTGS-associated DNA methylation signal is transmitted independent of a PTGS signal. |
format | Online Article Text |
id | pubmed-6753489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-67534892019-09-25 Post-transcriptional gene silencing triggers dispensable DNA methylation in gene body in Arabidopsis Taochy, Christelle Yu, Agnès Bouché, Nicolas Bouteiller, Nathalie Elmayan, Taline Dressel, Uwe Carroll, Bernard J Vaucheret, Hervé Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Spontaneous post-transcriptional silencing of sense transgenes (S-PTGS) is established in each generation and is accompanied by DNA methylation, but the pathway of PTGS-dependent DNA methylation is unknown and so is its role. Here we show that CHH and CHG methylation coincides spatially and temporally with RDR6-dependent products derived from the central and 3′ regions of the coding sequence, and requires the components of the RNA-directed DNA methylation (RdDM) pathway NRPE1, DRD1 and DRM2, but not CLSY1, NRPD1, RDR2 or DCL3, suggesting that RDR6-dependent products, namely long dsRNAs and/or siRNAs, trigger PTGS-dependent DNA methylation. Nevertheless, none of these RdDM components are required to establish S-PTGS or produce a systemic silencing signal. Moreover, preventing de novo DNA methylation in non-silenced transgenic tissues grafted onto homologous silenced tissues does not inhibit the triggering of PTGS. Overall, these data indicate that gene body DNA methylation is a consequence, not a cause, of PTGS, and rule out the hypothesis that a PTGS-associated DNA methylation signal is transmitted independent of a PTGS signal. Oxford University Press 2019-09-26 2019-08-02 /pmc/articles/PMC6753489/ /pubmed/31372641 http://dx.doi.org/10.1093/nar/gkz636 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Taochy, Christelle Yu, Agnès Bouché, Nicolas Bouteiller, Nathalie Elmayan, Taline Dressel, Uwe Carroll, Bernard J Vaucheret, Hervé Post-transcriptional gene silencing triggers dispensable DNA methylation in gene body in Arabidopsis |
title | Post-transcriptional gene silencing triggers dispensable DNA methylation in gene body in Arabidopsis |
title_full | Post-transcriptional gene silencing triggers dispensable DNA methylation in gene body in Arabidopsis |
title_fullStr | Post-transcriptional gene silencing triggers dispensable DNA methylation in gene body in Arabidopsis |
title_full_unstemmed | Post-transcriptional gene silencing triggers dispensable DNA methylation in gene body in Arabidopsis |
title_short | Post-transcriptional gene silencing triggers dispensable DNA methylation in gene body in Arabidopsis |
title_sort | post-transcriptional gene silencing triggers dispensable dna methylation in gene body in arabidopsis |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753489/ https://www.ncbi.nlm.nih.gov/pubmed/31372641 http://dx.doi.org/10.1093/nar/gkz636 |
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