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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.

DOI:10.1111/j.1365-2958.2007.05725.x
PMID:17542913
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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Characterization of a TFIIH homologue from Trypanosoma brucei.布氏锥虫TFIIH同源物的特性分析。
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Transcriptionally active TFIIH of the early-diverged eukaryote Trypanosoma brucei harbors two novel core subunits but not a cyclin-activating kinase complex.早期分化的真核生物布氏锥虫转录活性的TFIIH含有两个新的核心亚基,但不含有细胞周期蛋白激活激酶复合物。
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Trypanosoma brucei harbours a divergent XPB helicase paralogue that is specialized in nucleotide excision repair and conserved among kinetoplastid organisms.布氏锥虫含有一个在核苷酸切除修复中具有特殊功能的 XPB 解旋酶的分化同源物,并且在所有动基体目生物中都高度保守。
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TBP and SNAP50 transcription factors bind specifically to the Pr77 promoter sequence from trypanosomatid non-LTR retrotransposons.TBP 和 SNAP50 转录因子特异性结合于原虫非 LTR 反转录转座子的 Pr77 启动子序列。
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Transcription Factor Analysis in Trypanosomatids.
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The DNA damage response is developmentally regulated in the African trypanosome.DNA 损伤反应在非洲锥虫中受到发育调控。
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An RNA polymerase II-associated TFIIF-like complex is indispensable for SL RNA gene transcription in Trypanosoma brucei.RNA 聚合酶 II 相关的 TFIIF 样复合物对于布氏锥虫 SL RNA 基因转录是必不可少的。
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