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The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation
MORPHEUS’ MOLECULE1 (MOM1) is an Arabidopsis factor previously shown to mediate transcriptional silencing independent of major DNA methylation changes. Here we find that MOM1 localizes with sites of RNA-directed DNA methylation (RdDM). Tethering MOM1 with an artificial zinc finger to an unmethylated...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338684/ https://www.ncbi.nlm.nih.gov/pubmed/37438334 http://dx.doi.org/10.1038/s41467-023-39751-4 |
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author | Li, Zheng Wang, Ming Zhong, Zhenhui Gallego-Bartolomé, Javier Feng, Suhua Jami-Alahmadi, Yasaman Wang, Xinyi Wohlschlegel, James Bischof, Sylvain Long, Jeff A. Jacobsen, Steven E. |
author_facet | Li, Zheng Wang, Ming Zhong, Zhenhui Gallego-Bartolomé, Javier Feng, Suhua Jami-Alahmadi, Yasaman Wang, Xinyi Wohlschlegel, James Bischof, Sylvain Long, Jeff A. Jacobsen, Steven E. |
author_sort | Li, Zheng |
collection | PubMed |
description | MORPHEUS’ MOLECULE1 (MOM1) is an Arabidopsis factor previously shown to mediate transcriptional silencing independent of major DNA methylation changes. Here we find that MOM1 localizes with sites of RNA-directed DNA methylation (RdDM). Tethering MOM1 with an artificial zinc finger to an unmethylated FWA promoter leads to establishment of DNA methylation and FWA silencing. This process is blocked by mutations in components of the Pol V arm of the RdDM machinery, as well as by mutation of MICRORCHIDIA 6 (MORC6). We find that at some endogenous RdDM sites, MOM1 is required to maintain DNA methylation and a closed chromatin state. In addition, efficient silencing of newly introduced FWA transgenes is impaired in the mom1 mutant. In addition to RdDM sites, we identify a group of MOM1 peaks at active chromatin near genes that colocalized with MORC6. These findings demonstrate a multifaceted role of MOM1 in genome regulation. |
format | Online Article Text |
id | pubmed-10338684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103386842023-07-14 The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation Li, Zheng Wang, Ming Zhong, Zhenhui Gallego-Bartolomé, Javier Feng, Suhua Jami-Alahmadi, Yasaman Wang, Xinyi Wohlschlegel, James Bischof, Sylvain Long, Jeff A. Jacobsen, Steven E. Nat Commun Article MORPHEUS’ MOLECULE1 (MOM1) is an Arabidopsis factor previously shown to mediate transcriptional silencing independent of major DNA methylation changes. Here we find that MOM1 localizes with sites of RNA-directed DNA methylation (RdDM). Tethering MOM1 with an artificial zinc finger to an unmethylated FWA promoter leads to establishment of DNA methylation and FWA silencing. This process is blocked by mutations in components of the Pol V arm of the RdDM machinery, as well as by mutation of MICRORCHIDIA 6 (MORC6). We find that at some endogenous RdDM sites, MOM1 is required to maintain DNA methylation and a closed chromatin state. In addition, efficient silencing of newly introduced FWA transgenes is impaired in the mom1 mutant. In addition to RdDM sites, we identify a group of MOM1 peaks at active chromatin near genes that colocalized with MORC6. These findings demonstrate a multifaceted role of MOM1 in genome regulation. Nature Publishing Group UK 2023-07-12 /pmc/articles/PMC10338684/ /pubmed/37438334 http://dx.doi.org/10.1038/s41467-023-39751-4 Text en © The Author(s) 2023 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 Li, Zheng Wang, Ming Zhong, Zhenhui Gallego-Bartolomé, Javier Feng, Suhua Jami-Alahmadi, Yasaman Wang, Xinyi Wohlschlegel, James Bischof, Sylvain Long, Jeff A. Jacobsen, Steven E. The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation |
title | The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation |
title_full | The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation |
title_fullStr | The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation |
title_full_unstemmed | The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation |
title_short | The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation |
title_sort | mom1 complex recruits the rddm machinery via morc6 to establish de novo dna methylation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338684/ https://www.ncbi.nlm.nih.gov/pubmed/37438334 http://dx.doi.org/10.1038/s41467-023-39751-4 |
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