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Insight into the Architecture of the NuRD Complex: STRUCTURE OF THE RbAp48-MTA1 SUBCOMPLEX
The nucleosome remodeling and deacetylase (NuRD) complex is a widely conserved transcriptional co-regulator that harbors both nucleosome remodeling and histone deacetylase activities. It plays a critical role in the early stages of ES cell differentiation and the reprogramming of somatic to induced...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139204/ https://www.ncbi.nlm.nih.gov/pubmed/24920672 http://dx.doi.org/10.1074/jbc.M114.558940 |
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author | Alqarni, Saad S. M. Murthy, Andal Zhang, Wei Przewloka, Marcin R. Silva, Ana P. G. Watson, Aleksandra A. Lejon, Sara Pei, Xue Y. Smits, Arne H. Kloet, Susan L. Wang, Hongxin Shepherd, Nicholas E. Stokes, Philippa H. Blobel, Gerd A. Vermeulen, Michiel Glover, David M. Mackay, Joel P. Laue, Ernest D. |
author_facet | Alqarni, Saad S. M. Murthy, Andal Zhang, Wei Przewloka, Marcin R. Silva, Ana P. G. Watson, Aleksandra A. Lejon, Sara Pei, Xue Y. Smits, Arne H. Kloet, Susan L. Wang, Hongxin Shepherd, Nicholas E. Stokes, Philippa H. Blobel, Gerd A. Vermeulen, Michiel Glover, David M. Mackay, Joel P. Laue, Ernest D. |
author_sort | Alqarni, Saad S. M. |
collection | PubMed |
description | The nucleosome remodeling and deacetylase (NuRD) complex is a widely conserved transcriptional co-regulator that harbors both nucleosome remodeling and histone deacetylase activities. It plays a critical role in the early stages of ES cell differentiation and the reprogramming of somatic to induced pluripotent stem cells. Abnormalities in several NuRD proteins are associated with cancer and aging. We have investigated the architecture of NuRD by determining the structure of a subcomplex comprising RbAp48 and MTA1. Surprisingly, RbAp48 recognizes MTA1 using the same site that it uses to bind histone H4, showing that assembly into NuRD modulates RbAp46/48 interactions with histones. Taken together with other results, our data show that the MTA proteins act as scaffolds for NuRD complex assembly. We further show that the RbAp48-MTA1 interaction is essential for the in vivo integration of RbAp46/48 into the NuRD complex. |
format | Online Article Text |
id | pubmed-4139204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41392042014-08-25 Insight into the Architecture of the NuRD Complex: STRUCTURE OF THE RbAp48-MTA1 SUBCOMPLEX Alqarni, Saad S. M. Murthy, Andal Zhang, Wei Przewloka, Marcin R. Silva, Ana P. G. Watson, Aleksandra A. Lejon, Sara Pei, Xue Y. Smits, Arne H. Kloet, Susan L. Wang, Hongxin Shepherd, Nicholas E. Stokes, Philippa H. Blobel, Gerd A. Vermeulen, Michiel Glover, David M. Mackay, Joel P. Laue, Ernest D. J Biol Chem Gene Regulation The nucleosome remodeling and deacetylase (NuRD) complex is a widely conserved transcriptional co-regulator that harbors both nucleosome remodeling and histone deacetylase activities. It plays a critical role in the early stages of ES cell differentiation and the reprogramming of somatic to induced pluripotent stem cells. Abnormalities in several NuRD proteins are associated with cancer and aging. We have investigated the architecture of NuRD by determining the structure of a subcomplex comprising RbAp48 and MTA1. Surprisingly, RbAp48 recognizes MTA1 using the same site that it uses to bind histone H4, showing that assembly into NuRD modulates RbAp46/48 interactions with histones. Taken together with other results, our data show that the MTA proteins act as scaffolds for NuRD complex assembly. We further show that the RbAp48-MTA1 interaction is essential for the in vivo integration of RbAp46/48 into the NuRD complex. American Society for Biochemistry and Molecular Biology 2014-08-08 2014-06-11 /pmc/articles/PMC4139204/ /pubmed/24920672 http://dx.doi.org/10.1074/jbc.M114.558940 Text en © 2014 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/) applies to Author Choice Articles |
spellingShingle | Gene Regulation Alqarni, Saad S. M. Murthy, Andal Zhang, Wei Przewloka, Marcin R. Silva, Ana P. G. Watson, Aleksandra A. Lejon, Sara Pei, Xue Y. Smits, Arne H. Kloet, Susan L. Wang, Hongxin Shepherd, Nicholas E. Stokes, Philippa H. Blobel, Gerd A. Vermeulen, Michiel Glover, David M. Mackay, Joel P. Laue, Ernest D. Insight into the Architecture of the NuRD Complex: STRUCTURE OF THE RbAp48-MTA1 SUBCOMPLEX |
title | Insight into the Architecture of the NuRD Complex: STRUCTURE OF THE RbAp48-MTA1 SUBCOMPLEX |
title_full | Insight into the Architecture of the NuRD Complex: STRUCTURE OF THE RbAp48-MTA1 SUBCOMPLEX |
title_fullStr | Insight into the Architecture of the NuRD Complex: STRUCTURE OF THE RbAp48-MTA1 SUBCOMPLEX |
title_full_unstemmed | Insight into the Architecture of the NuRD Complex: STRUCTURE OF THE RbAp48-MTA1 SUBCOMPLEX |
title_short | Insight into the Architecture of the NuRD Complex: STRUCTURE OF THE RbAp48-MTA1 SUBCOMPLEX |
title_sort | insight into the architecture of the nurd complex: structure of the rbap48-mta1 subcomplex |
topic | Gene Regulation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139204/ https://www.ncbi.nlm.nih.gov/pubmed/24920672 http://dx.doi.org/10.1074/jbc.M114.558940 |
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