Rüth J, Conesa C, Dieci G, Lefebvre O, Düsterhöft A, Ottonello S, Sentenac A
Service de Biochimie et de Génétique Moléculaire, CEA-Centre d'Etudes de Saclay, Gif-sur-Yvette, France.
EMBO J. 1996 Apr 15;15(8):1941-9.
Class III genes depend on TFIIIB for recruitment of RNA polymerase III. Yeast TFIIIB is comprised of three components: TBP, TFIIIB70 and a 90 kDa polypeptide contained in the fraction B". We report the isolation of the yeast gene TFC7 which, based on genetic and biochemical evidence, encodes the 90 kDa polypeptide. TFC7 was isolated as a multicopy suppressor of temperature-sensitive mutations in the two largest subunits of TFIIIC. It is an essential gene, encoding a polypeptide of 68 kDa migrating with an apparent size of approximately 90 kDa. In gel shift assays, recombinant TFC7 protein (rTFC7) alone did not bind detectably to DNA, or to the TFIIIC-DNA complex even in the presence of TBP or TFIIIB70, but it was required to assemble the TFIIIB-TFIIIC-DNA complex. The two-hybrid assay pointed to an interaction between TFC7 protein and tau 131, the second largest subunit of TFIIIC (that also interacts with TFIIIB70). rTFC7p can replace the B" component of TFIIIB for synthesis of U6 RNA in a system reconstituted with recombinant TBP and TFIIIB70 polypeptides and highly purified RNA polymerase III. Surprisingly, specific transcription of the SUP4 tRNATyr gene promoted by rTFC7p was much weaker than with B". An additional factor activity, provided by the recently identified TFIIIE fraction, was required to restore control levels of transcription.
III类基因依赖TFIIIB来招募RNA聚合酶III。酵母TFIIIB由三个组分组成:TBP、TFIIIB70和包含在B”组分中的一种90 kDa多肽。我们报道了酵母基因TFC7的分离,基于遗传和生化证据,该基因编码90 kDa多肽。TFC7是作为TFIIIC两个最大亚基温度敏感突变的多拷贝抑制子分离得到的。它是一个必需基因,编码一种68 kDa的多肽,迁移时表观大小约为90 kDa。在凝胶迁移实验中,单独的重组TFC7蛋白(rTFC7)即使在存在TBP或TFIIIB70的情况下也不能检测到与DNA或TFIIIC-DNA复合物结合,但它是组装TFIIIB-TFIIIC-DNA复合物所必需的。双杂交实验表明TFC7蛋白与TFIIIC的第二大亚基tau 131之间存在相互作用(tau 131也与TFIIIB70相互作用)。在由重组TBP和TFIIIB70多肽以及高度纯化的RNA聚合酶III重构的系统中,rTFC7p可以替代TFIIIB的B”组分用于U6 RNA的合成。令人惊讶的是,rTFC7p促进的SUP4 tRNATyr基因的特异性转录比B”弱得多。需要由最近鉴定的TFIIIE组分提供的另一种因子活性来恢复转录的对照水平。