Berroteran R W, Ware D E, Hampsey M
Department of Biochemistry and Molecular Biology, Louisiana State University Medical Center, Shreveport 71130.
Mol Cell Biol. 1994 Jan;14(1):226-37. doi: 10.1128/mcb.14.1.226-237.1994.
Mutations in the Saccharomyces cerevisiae sua8 gene were found to be suppressors of an aberrant ATG translation initiation codon in the leader region of the cyc1 gene. Analysis of cyc1 transcripts from sua8 mutants revealed that suppression is a consequence of diminished transcription initiation at the normal start sites in favor of initiation at downstream sites, including a site between the aberrant and normal ATG start codons. This effect is not cyc1 gene specific since initiation at other genes, including ADH1, CYC7, and HIS4, was similarly affected, although initiation at HIS3 and SPT15 was unaffected. The SUA8 gene was cloned and partially sequenced, revealing identity to RPB1, which encodes the largest subunit of RNA polymerase II. The sua8 suppressors are the result of single amino acid replacements of highly conserved residues. Three replacements were found either within or immediately preceding homology block D, and a fourth was found adjacent to homology block H, indicating that these regions play a role in defining start sites in vivo. Nearly identical effects on start site selection were observed for sua7 suppressors, which encode altered forms of TFIIB. Synthetic lethality was associated with double sua7 sua8 suppressor mutations, and recessive sua7 mutants failed to fully complement recessive sua8 mutants in heterozygous diploids (nonallelic noncomplementation). These data indicate that the largest subunit of RNA polymerase II and TFIIB are important determinants of transcription start site selection in S. cerevisiae and suggest that this function might be conferred by interaction between these two proteins.
已发现酿酒酵母sua8基因中的突变是cyc1基因前导区异常ATG翻译起始密码子的抑制子。对来自sua8突变体的cyc1转录本分析表明,抑制作用是正常起始位点转录起始减少,转而有利于下游位点起始的结果,这些下游位点包括异常和正常ATG起始密码子之间的一个位点。这种效应并非cyc1基因所特有,因为包括ADH1、CYC7和HIS4在内的其他基因的起始也受到类似影响,尽管HIS3和SPT15的起始不受影响。SUA基因被克隆并进行了部分测序,结果显示其与编码RNA聚合酶II最大亚基的RPB1相同。sua8抑制子是高度保守残基的单个氨基酸替换的结果。在同源结构域D内或其紧邻前方发现了三个替换,在同源结构域H附近发现了第四个替换,这表明这些区域在体内确定起始位点中发挥作用。对于编码改变形式TFIIB的sua7抑制子,观察到对起始位点选择几乎相同的影响。合成致死性与双sua7 sua8抑制子突变相关,并且隐性sua7突变体在杂合二倍体中不能完全互补隐性sua8突变体(非等位基因非互补)。这些数据表明RNA聚合酶II的最大亚基和TFIIB是酿酒酵母转录起始位点选择的重要决定因素,并表明这种功能可能由这两种蛋白质之间的相互作用赋予。