Drosophila MCRS2 Associates with RNA Polymerase II Complexes To Regulate Transcription

被引:19
|
作者
Andersen, Ditte Skovaa [1 ,2 ]
Raja, Sunil Jayaramaiah [3 ,4 ]
Colombani, Julien [1 ,2 ]
Shaw, Rachael Louise [1 ]
Langton, Paul Francis [1 ,5 ]
Akhtar, Asifa [3 ,4 ]
Tapon, Nicolas [1 ]
机构
[1] Canc Res UK, London Res Inst, Apoptosis & Proliferat Control Lab, London WC2A 3PX, England
[2] CNRS, Inst Signaling Dev Biol & Canc, UMR 6543, F-06108 Nice 2, France
[3] European Mol Biol Lab, Gene Express Unit, D-69117 Heidelberg, Germany
[4] Max Planck Inst Immunobiol, D-79108 Freiburg, Germany
[5] MRC Natl Inst Med Res, London NW7 1AA, England
关键词
CARBOXYL-TERMINAL DOMAIN; PROTEIN-CODING GENES; DOSAGE COMPENSATION; HISTONE H4; FHA DOMAIN; MSL COMPLEX; MOF; ELONGATION; CELLS; ACETYLTRANSFERASE;
D O I
10.1128/MCB.01586-09
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:4744 / 4755
页数:12
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