Peñate Xenia, López-Farfán Diana, Landeira David, Wentland Amy, Vidal Isabel, Navarro Miguel
Instituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas, CSIC (Spanish National Research Council), Avda. del Conocimiento s/n, 18100 Granada, Spain.
EMBO Rep. 2009 Mar;10(3):252-7. doi: 10.1038/embor.2008.244. Epub 2009 Jan 23.
In the protozoan parasite Trypanosoma brucei, the two main surface glycoprotein genes are transcribed by RNA polymerase I (pol I) instead of RNA pol II, the polymerase committed to the production of mRNA in eukaryotes. This unusual feature might be accomplished by the recruitment of specific subunits or cofactors that allow pol I to transcribe protein-coding RNAs. Here, we report that transcription mediated by pol I requires TbRPB7, a dissociable subunit of the pol II complex. TbRPB7 was found to interact with two pol I-specific subunits, TbRPA1 and TbRPB6z. Pol I-specific transcription was affected on depletion of TbRPB7 in run-on assays, whereas recombinant TbRPB7 increased transcription driven by a pol I promoter. These results represent a unique example of a functional RNA polymerase chimaera consisting of a core pol I complex that recruits a specific pol II subunit.
在原生动物寄生虫布氏锥虫中,两个主要的表面糖蛋白基因由RNA聚合酶I(pol I)转录,而不是由负责在真核生物中产生mRNA的RNA聚合酶II转录。这种不寻常的特征可能是通过招募特定的亚基或辅助因子来实现的,这些亚基或辅助因子使pol I能够转录蛋白质编码RNA。在此,我们报告由pol I介导的转录需要TbRPB7,它是pol II复合物的一个可解离亚基。发现TbRPB7与两个pol I特异性亚基TbRPA1和TbRPB6z相互作用。在连续转录分析中,TbRPB7缺失会影响pol I特异性转录,而重组TbRPB7则增加了由pol I启动子驱动的转录。这些结果代表了一个功能性RNA聚合酶嵌合体的独特例子,该嵌合体由一个招募特定pol II亚基的核心pol I复合物组成。