Drosophila MCRS2 Associates with RNA Polymerase II Complexes To Regulate Transcription

Author:

Andersen Ditte Skovaa12,Raja Sunil Jayaramaiah34,Colombani Julien12,Shaw Rachael Louise1,Langton Paul Francis15,Akhtar Asifa34,Tapon Nicolas1

Affiliation:

1. Apoptosis and Proliferation Control Laboratory, Cancer Research UK, London Research Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, United Kingdom

2. Institute for Signaling, Developmental Biology and Cancer, Centre National de la Recherche Scientifique Unité Mixte de Recherche 6543, Parc Valrose, 06108 Nice Cedex 2, France

3. Genome Biology, Gene Expression Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany

4. Max-Planck-Institut für Immunbiologie, Stübeweg 51, 79108 Freiburg im Breisgau, Germany

5. MRC National Institute for Medical Research, Mill Hill, London NW7 1AA, United Kingdom

Abstract

ABSTRACT Drosophila MCRS2 (dMCRS2; MCRS2/MSP58 and its splice variant MCRS1/p78 in humans) belongs to a family of forkhead-associated (FHA) domain proteins. Whereas human MCRS2 proteins have been associated with a variety of cellular processes, including RNA polymerase I transcription and cell cycle progression, dMCRS2 has been largely uncharacterized. Recent data show that MCRS2 is purified as part of a complex containing the histone acetyltransferase MOF (males absent on first) in both humans and flies. MOF mediates H4K16 acetylation and regulates the expression of a large number of genes, suggesting that MCRS2 could also have a function in transcription regulation. Here, we show that dMCRS2 copurifies with RNA polymerase II (RNAP II) complexes and localizes to the 5′ ends of genes. Moreover, dMCRS2 is required for optimal recruitment of RNAP II to the promoter regions of cyclin genes. In agreement with this, dMCRS2 is required for normal levels of cyclin gene expression. We propose a model whereby dMCRS2 promotes gene transcription by facilitating the recruitment of RNAP II preinitiation complexes (PICs) to the promoter regions of target genes.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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