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ACD15, ACD21 and SLN regulate 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: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473691/ https://www.ncbi.nlm.nih.gov/pubmed/37662299 http://dx.doi.org/10.1101/2023.08.23.554494 |
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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 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 complex components 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 massive accumulation of MBD5/6 complexes into large nuclear bodies. These results demonstrate that ACD15 and ACD21 are critical components of gene silencing complexes that act to drive the formation of higher order, dynamic assemblies. |
format | Online Article Text |
id | pubmed-10473691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104736912023-09-02 ACD15, ACD21 and SLN regulate 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. bioRxiv Article 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 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 complex components 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 massive accumulation of MBD5/6 complexes into large nuclear bodies. These results demonstrate that ACD15 and ACD21 are critical components of gene silencing complexes that act to drive the formation of higher order, dynamic assemblies. Cold Spring Harbor Laboratory 2023-10-06 /pmc/articles/PMC10473691/ /pubmed/37662299 http://dx.doi.org/10.1101/2023.08.23.554494 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article 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 accumulation and mobility of MBD6 to silence genes and transposable elements |
title | ACD15, ACD21 and SLN regulate accumulation and mobility of MBD6 to silence genes and transposable elements |
title_full | ACD15, ACD21 and SLN regulate accumulation and mobility of MBD6 to silence genes and transposable elements |
title_fullStr | ACD15, ACD21 and SLN regulate accumulation and mobility of MBD6 to silence genes and transposable elements |
title_full_unstemmed | ACD15, ACD21 and SLN regulate accumulation and mobility of MBD6 to silence genes and transposable elements |
title_short | ACD15, ACD21 and SLN regulate accumulation and mobility of MBD6 to silence genes and transposable elements |
title_sort | acd15, acd21 and sln regulate accumulation and mobility of mbd6 to silence genes and transposable elements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473691/ https://www.ncbi.nlm.nih.gov/pubmed/37662299 http://dx.doi.org/10.1101/2023.08.23.554494 |
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