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ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements
DNA methylation mediates silencing of transposable elements and genes in part via recruitment of the Arabidopsis MBD5/6 complex, which contains the methyl-CpG binding domain (MBD) proteins MBD5 and MBD6, and the J-domain containing protein SILENZIO (SLN). Here, we characterize two additional complex...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651127/ https://www.ncbi.nlm.nih.gov/pubmed/37967186 http://dx.doi.org/10.1126/sciadv.adi9036 |
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author | Boone, Brandon A. Ichino, Lucia Wang, Shuya Gardiner, Jason Yun, Jaewon Jami-Alahmadi, Yasaman Sha, Jihui Mendoza, Cristy P. Steelman, Bailey J. van Aardenne, Aliya Kira-Lucas, Sophia Trentchev, Isabelle Wohlschlegel, James A. Jacobsen, Steven E. |
author_facet | Boone, Brandon A. Ichino, Lucia Wang, Shuya Gardiner, Jason Yun, Jaewon Jami-Alahmadi, Yasaman Sha, Jihui Mendoza, Cristy P. Steelman, Bailey J. van Aardenne, Aliya Kira-Lucas, Sophia Trentchev, Isabelle Wohlschlegel, James A. Jacobsen, Steven E. |
author_sort | Boone, Brandon A. |
collection | PubMed |
description | DNA methylation mediates silencing of transposable elements and genes in part via recruitment of the Arabidopsis MBD5/6 complex, which contains the methyl-CpG binding domain (MBD) proteins MBD5 and MBD6, and the J-domain containing protein SILENZIO (SLN). Here, we characterize two additional complex members: α-crystalline domain (ACD) containing proteins ACD15 and ACD21. We show that they are necessary for gene silencing, bridge SLN to the complex, and promote higher-order multimerization of MBD5/6 complexes within heterochromatin. These complexes are also highly dynamic, with the mobility of MBD5/6 complexes regulated by the activity of SLN. Using a dCas9 system, we demonstrate that tethering the ACDs to an ectopic site outside of heterochromatin can drive a massive accumulation of MBD5/6 complexes into large nuclear bodies. These results demonstrate that ACD15 and ACD21 are critical components of the gene-silencing MBD5/6 complex and act to drive the formation of higher-order, dynamic assemblies at CG methylation (meCG) sites. |
format | Online Article Text |
id | pubmed-10651127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106511272023-11-15 ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements Boone, Brandon A. Ichino, Lucia Wang, Shuya Gardiner, Jason Yun, Jaewon Jami-Alahmadi, Yasaman Sha, Jihui Mendoza, Cristy P. Steelman, Bailey J. van Aardenne, Aliya Kira-Lucas, Sophia Trentchev, Isabelle Wohlschlegel, James A. Jacobsen, Steven E. Sci Adv Biomedicine and Life Sciences DNA methylation mediates silencing of transposable elements and genes in part via recruitment of the Arabidopsis MBD5/6 complex, which contains the methyl-CpG binding domain (MBD) proteins MBD5 and MBD6, and the J-domain containing protein SILENZIO (SLN). Here, we characterize two additional complex members: α-crystalline domain (ACD) containing proteins ACD15 and ACD21. We show that they are necessary for gene silencing, bridge SLN to the complex, and promote higher-order multimerization of MBD5/6 complexes within heterochromatin. These complexes are also highly dynamic, with the mobility of MBD5/6 complexes regulated by the activity of SLN. Using a dCas9 system, we demonstrate that tethering the ACDs to an ectopic site outside of heterochromatin can drive a massive accumulation of MBD5/6 complexes into large nuclear bodies. These results demonstrate that ACD15 and ACD21 are critical components of the gene-silencing MBD5/6 complex and act to drive the formation of higher-order, dynamic assemblies at CG methylation (meCG) sites. American Association for the Advancement of Science 2023-11-15 /pmc/articles/PMC10651127/ /pubmed/37967186 http://dx.doi.org/10.1126/sciadv.adi9036 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Boone, Brandon A. Ichino, Lucia Wang, Shuya Gardiner, Jason Yun, Jaewon Jami-Alahmadi, Yasaman Sha, Jihui Mendoza, Cristy P. Steelman, Bailey J. van Aardenne, Aliya Kira-Lucas, Sophia Trentchev, Isabelle Wohlschlegel, James A. Jacobsen, Steven E. ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements |
title | ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements |
title_full | ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements |
title_fullStr | ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements |
title_full_unstemmed | ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements |
title_short | ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements |
title_sort | acd15, acd21, and sln regulate the accumulation and mobility of mbd6 to silence genes and transposable elements |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651127/ https://www.ncbi.nlm.nih.gov/pubmed/37967186 http://dx.doi.org/10.1126/sciadv.adi9036 |
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