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Structure and function insights into the NuRD chromatin remodeling complex

期刊

CELLULAR AND MOLECULAR LIFE SCIENCES
卷 72, 期 13, 页码 2491-2507

出版社

SPRINGER BASEL AG
DOI: 10.1007/s00018-015-1880-8

关键词

NuRD; Remodeling; Deacetylase; Chromatin; Nucleosome; Structural biology

资金

  1. Fondation pour la Recherche Medicale (FRM)
  2. Agence Nationale pour la Recherche (ANR)
  3. Association pour la Recherche sur le Cancer (ARC)
  4. Centre Nationale pour la Recherche Scientifique (CNRS)
  5. French Infrastructure for Integrated Structural Biology (FRISBI) [ANR-10-INSB-05-01]
  6. Instruct as part of the European Strategy Forum on Research Infrastructures (ESFRI)

向作者/读者索取更多资源

Transcription regulation through chromatin compaction and decompaction is regulated through various chromatin-remodeling complexes such as nucleosome remodeling and histone deacetylation (NuRD) complex. NuRD is a 1 MDa multi-subunit protein complex which comprises many different subunits, among which histone deacetylases HDAC1/2, ATP-dependent remodeling enzymes CHD3/4, histone chaperones RbAp46/48, CpG-binding proteins MBD2/3, the GATAD2a (p66 alpha) and/or GATAD2b (p66 beta) and specific DNA-binding proteins MTA1/2/3. Here, we review the currently known crystal and NMR structures of these subunits, the functional data and their relevance for biomedical research considering the implication of NuRD subunits in cancer and various other diseases. The complexity of this macromolecular assembly, and its poorly understood mode of interaction with the nucleosome, the repeating unit of chromatin, illustrate that this complex is a major challenge for structure-function relationship studies which will be tackled best by an integrated biology approach.

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