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布氏锥虫TFIIH同源物的特性分析。

Characterization of a TFIIH homologue from Trypanosoma brucei.

作者信息

Lecordier Laurence, Devaux Sara, Uzureau Pierrick, Dierick Jean François, Walgraffe David, Poelvoorde Philippe, Pays Etienne, Vanhamme Luc

机构信息

Laboratory of Molecular Parasitology, Institute of Molecular Biology and Medicine, Université Libre de Bruxelles, 12, rue des Professeurs Jeener et Brachet, B-6041 Gosselies, Belgium.

出版信息

Mol Microbiol. 2007 Jun;64(5):1164-81. doi: 10.1111/j.1365-2958.2007.05725.x.

Abstract

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.

摘要

锥虫是具有独特转录特征的原生动物。我们在布氏锥虫中描述了一种与TFIIH同源的复合体,TFIIH是一种多亚基转录因子,参与RNA聚合酶I和RNA聚合酶II对转录的调控,同时也参与DNA修复和细胞周期调控。生物信息学分析检测到五个编码四个假定核心TFIIH亚基(TbXPD、TbXPB、Tbp44、Tbp52)的基因,包括一个新的XPB变体TbXPBz。在所有情况下,已知对TFIIH功能重要的序列都是保守的。我们对这个核心复合体进行了分子分析,重点关注赋予已知酶活性(解旋酶)的两个亚基XPD和XPB。这些布氏锥虫蛋白参与真正的TFIIH核心复合体得到了以下支持:(i)通过免疫荧光在细胞核中共定位;(ii)通过双杂交试验和核心TFIIH的串联亲和纯化确定TbXPD与其相互作用的调节亚基Tbp44直接物理相互作用;(iii)核心蛋白参与高分子量复合体;(iv)在RNAi敲低或必需亚基过表达时出现转录、细胞周期和DNA修复表型。

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