Characterization of a TFIIH homologue from Trypanosoma brucei

被引:31
作者
Lecordier, Laurence
Devaux, Sara
Uzureau, Pierrick
Dierick, Jean Francois
Walgraffe, David
Poelvoorde, Philippe
Pays, Etienne
Vanhamme, Luc
机构
[1] Univ Libre Bruxelles, Inst Mol Biol & Med, Mol Parasitol Lab, B-6041 Gosselies, Belgium
[2] BioVallee, Prote Unit, Gosselies, Belgium
关键词
D O I
10.1111/j.1365-2958.2007.05725.x
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
Trypanosomes are protozoans showing unique transcription characteristics. We describe in Trypanosoma brucei a complex homologous to TFIIH, a multisubunit transcription factor involved in the control of transcription by RNA Pol I and RNA Pol II, but also in DNA repair and cell cycle control. Bioinformatics analyses allowed the detection of five genes encoding four putative core TFIIH subunits (TbXPD, TbXPB, Tbp44, Tbp52), including a novel XPB variant, TbXPBz. In all cases sequences known to be important for TFIIH functions were conserved. We performed a molecular analysis of this core complex, focusing on the two subunits endowed with a known enzymatic (helicase) activity, XPD and XPB. The involvement of these T. brucei proteins in a bona fide TFIIH core complex was supported by (i) colocalization by immunofluorescence in the nucleus, (ii) direct physical interaction of TbXPD and its interacting regulatory subunit Tbp44 as determined by double-hybrid assay and tandem affinity purification of the core TFIIH, (iii) involvement of the core proteins in a high molecular weight complex and (iv) occurrence of transcription, cell cycle and DNA repair phenotypes upon either RNAi knock-down or overexpression of essential subunits.
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收藏
页码:1164 / 1181
页数:18
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