Literature DB >> 19923891

The Mi-2/NuRD complex: a critical epigenetic regulator of hematopoietic development, differentiation and cancer.

Julita Ramírez1, James Hagman.   

Abstract

The Mi-2/NuRD chromatin remodeling complex links multiple transcriptional regulatory processes including histone deacetylation, histone demethylation, nucleosome mobilization and recruitment of other regulatory proteins. In some contexts, Mi-2/NuRD functions as a barrier to transcriptional activation by working in opposition to other chromatin remodelers such as SWI/SNF. Alternatively, the Mi-2beta ATPase subunit of Mi-2/NuRD can promote transcription. Together, these gatekeeper functions of Mi-2/NuRD influence cell fate decisions by modulating transcriptional activity. Recent studies have shown the importance of Mi-2/NuRD both in maintaining hematopoietic stem cell (HSC) pools and in normal lineage progression. Furthermore, components of Mi-2/NuRD complexes are modular co-repressors/co-activators comprising multiple protein subunits that have been linked directly to oncogenesis and have potential as therapeutic targets for cancer treatment. Mi-2/NuRD's essential functions in metazoan cell fates and activities underscore its importance as a focal point of epigenetic research.

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Year:  2009        PMID: 19923891     DOI: 10.4161/epi.4.8.10108

Source DB:  PubMed          Journal:  Epigenetics        ISSN: 1559-2294            Impact factor:   4.528


  47 in total

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Review 6.  Cancer biology and NuRD: a multifaceted chromatin remodelling complex.

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Review 8.  Damage site chromatin: open or closed?

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9.  Sox2 uses multiple domains to associate with proteins present in Sox2-protein complexes.

Authors:  Jesse L Cox; Sunil K Mallanna; Xu Luo; Angie Rizzino
Journal:  PLoS One       Date:  2010-11-12       Impact factor: 3.240

10.  Regulation of DNA-damage responses and cell-cycle progression by the chromatin remodelling factor CHD4.

Authors:  Sophie E Polo; Abderrahmane Kaidi; Linda Baskcomb; Yaron Galanty; Stephen P Jackson
Journal:  EMBO J       Date:  2010-08-06       Impact factor: 11.598

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