dMec: A novel Mi-2 chromatin remodelling complex involved in transcriptional repression

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Abstract

The ATP-dependent chromatin remodeller Mi-2 functions as a transcriptional repressor and contributes to the suppression of cell fates during development in several model organisms. Mi-2 is the ATPase subunit of the conserved Nucleosome Remodeling and Deacetylation (NuRD) complex, and transcriptional repression by Mi-2 is thought to be dependent on its associated histone deacetylase. Here, we have purified a novel dMi-2 complex from Drosophila that is distinct from dNuRD. dMec (dMEP-1 complex) is composed of dMi-2 and dMEP-1. dMec is a nucleosome-stimulated ATPase that is expressed in embryos, larval tissues and adult flies. Surprisingly, dMec is far more abundant than dNuRD and constitutes the major dMi-2-containing complex. Both dNuRD and dMec associate with proneural genes of the achaete-scute complex. However, despite lacking a histone deacetylase subunit, only dMec contributes to the repression of proneural genes. These results reveal an unexpected complexity in the composition and function of Mi-2 complexes. ©2009 European Molecular Biology Organization.

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APA

Kunert, N., Wagner, E., Murawska, M., Klinker, H., Kremmer, E., & Brehm, A. (2009). dMec: A novel Mi-2 chromatin remodelling complex involved in transcriptional repression. EMBO Journal, 28(5), 533–544. https://doi.org/10.1038/emboj.2009.3

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