Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
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
_version_ 1785147597556547584
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
work_keys_str_mv AT boonebrandona acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT ichinolucia acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT wangshuya acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT gardinerjason acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT yunjaewon acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT jamialahmadiyasaman acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT shajihui acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT mendozacristyp acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT steelmanbaileyj acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT vanaardennealiya acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT kiralucassophia acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT trentchevisabelle acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT wohlschlegeljamesa acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements
AT jacobsenstevene acd15acd21andslnregulatetheaccumulationandmobilityofmbd6tosilencegenesandtransposableelements