Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/15096
Title: Network of phosphatases and HDAC complexes at repressed chromatin.
Authors: De Castro, I
Amin, H
Vinciotti, V
Vagnarelli, P
Issue Date: 2017
Citation: Cell Cycle, (2017)
Abstract: Tight regulation of gene expression is achieved by a variety of protein complexes that selectively bind chromatin, modify it and change its transcription competency. Histone acetylases (HATs) and deacetylases (HDAC) play an important role in this process. They can generate transcriptionally active or inactive chromatin through the addition (HATs) or removal (HDACs) of acetyl groups on histones, respectively. Repo-Man is a Protein Phosphatase 1 targeting subunit that accumulates on chromosomes during mitotic exit and mediates the removal of mitotic histone H3 phosphorylations. It was shown recently that Repo-Man also regulates heterochromatin formation in interphase and that its depletion favours the switch between transcriptionally inactive and active chromatin, demonstrating that its role goes well beyond mitosis. Here, we provide the first link between a phosphatase and HDAC complexes. We show that genome-wide Repo-Man binding sites overlap with chromatin regions bound by members of the three HDAC complexes (Sin3a, NuRD and CoREST). We establish that members of the NuRD and Sin3a HDAC complexes interact with Repo-Man by mass spectrometry and that Repo-Man is in close proximity to Sap18 (Sin3a) in interphase by the Proximity Ligation Assay. Altogether, these data suggest a mechanism by which Repo-Man/PP1 complex, via interactions with HDACs, could stabilise gene repression
URI: http://bura.brunel.ac.uk/handle/2438/15096
DOI: http://dx.doi.org/10.1080/15384101.2017.1371883
ISSN: 1538-4101
Appears in Collections:Dept of Life Sciences Embargoed Research Papers

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