Andrau J C, Sentenac A, Werner M
Service de Biochimie et Génétique Moléculaire, Bât. 142, CEA/Saclay, F-91191 Gif-sur-Yvette, CEDEX, France.
J Mol Biol. 1999 May 14;288(4):511-20. doi: 10.1006/jmbi.1999.2724.
The yeast TFIIIB transcription factor is composed of three components, TBP, TFIIIB90 or B", and TFIIIB70 or BRF. TFIIIB70 is a pivotal component since it interacts with TBP, TFIIIC and RNA polymerase III (pol III). In order to better understand the role of TFIIIB70, we mutagenized extensively three evolutionary conserved motifs of its pol III-specific C-terminal extension. Conditional mutations lying in conserved regions II and III were obtained, some of which altered the interaction with the C34 subunit of pol III and were co-lethal with rpc34 mutations. Two conditional mutations in region II impaired the interaction with TBP and were suppressed by its overexpression. The pattern of suppression of the strongest mutation by overexpression of various mutant TBP, suggested a contact between TBP-R220 and TFIIIB70-D464 residues in vivo. As expected, this TFIIIB70 mutation impaired the assembly of TFIIIB. TFIIIC.DNA complexes and affected in vitro transcription of the SUP4 tRNA gene. Our results underscore the important role of region II of TFIIIB70 in pre-initiation as well as transcription complex assembly via C34 and TBP binding.
酵母TFIIIB转录因子由三个组分组成,即TBP、TFIIIB90或B"以及TFIIIB70或BRF。TFIIIB70是关键组分,因为它与TBP、TFIIIC和RNA聚合酶III(pol III)相互作用。为了更好地理解TFIIIB70的作用,我们对其pol III特异性C末端延伸的三个进化保守基序进行了广泛诱变。获得了位于保守区域II和III的条件性突变,其中一些改变了与pol III的C34亚基的相互作用,并与rpc34突变具有共致死性。区域II中的两个条件性突变损害了与TBP的相互作用,并被其过表达所抑制。各种突变型TBP过表达对最强突变的抑制模式表明,体内TBP-R220与TFIIIB70-D464残基之间存在接触。正如预期的那样,这种TFIIIB70突变损害了TFIIIB的组装、TFIIIC-DNA复合物,并影响了SUP4 tRNA基因的体外转录。我们的结果强调了TFIIIB70区域II在起始前以及通过C34和TBP结合进行转录复合物组装中的重要作用。