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sua7突变的特征鉴定确定了酵母中参与转录起始位点选择的TFIIB结构域。

Characterization of sua7 mutations defines a domain of TFIIB involved in transcription start site selection in yeast.

作者信息

Pinto I, Wu W H, Na J G, Hampsey M

机构信息

Department of Biochemistry and Molecular Biology, Louisiana State University Medical Center, Shreveport 71130.

出版信息

J Biol Chem. 1994 Dec 2;269(48):30569-73.

PMID:7982976
Abstract

The SUA7 gene of Saccharomyces cerevisiae encodes the general transcription factor TFIIB. SUA7 was identified based on the ability of mutations at this locus to shift transcription start site selection at the cyc1 gene downstream of normal. Here, we report the nature of these mutations; the sua7-1 and sua7-2 alleles encode identical E62K replacements, and sua7-3 encodes an R78C replacement. Both Glu-62 and Arg-78 are phylogenetically invariant and occur within the most highly conserved region of TFIIB, immediately distal to a zinc finger motif. A double E62K,R78C mutant was constructed and exhibited the same phenotypes associated with the single mutants, including cold sensitivity and altered start site selection, suggesting that Glu-62 and Arg-78 are functionally related. This observation, and the opposite charge of the 2 residues, suggested that Glu-62 and Arg-78 might interact to form a salt bridge. This was tested by constructing reciprocal E62R and R78E replacements. The E62R mutant is phenotypically identical to the E62K mutant, whereas the R78E mutant is inviable. However, an E62R,R78E double mutant was not only viable but is phenotypically similar to the single mutants. These results define the highly conserved sequence adjacent to the zinc finger of TFIIB as a critical determinant of start site selection and suggest that an Glu-62-Arg-78 salt bridge is an important structural element of that domain.

摘要

酿酒酵母的SUA7基因编码通用转录因子TFIIB。SUA7是根据该位点的突变能够使正常情况下cyc1基因下游的转录起始位点选择发生偏移的能力而鉴定出来的。在此,我们报告这些突变的性质;sua7-1和sua7-2等位基因编码相同的E62K替换,而sua7-3编码R78C替换。Glu-62和Arg-78在系统发育上是不变的,并且位于TFIIB最保守区域内,紧邻锌指基序。构建了一个双E62K、R78C突变体,其表现出与单突变体相同的表型,包括冷敏感性和起始位点选择改变,这表明Glu-62和Arg-78在功能上相关。这一观察结果以及这两个残基的相反电荷表明,Glu-62和Arg-78可能相互作用形成盐桥。通过构建相互的E62R和R78E替换对此进行了测试。E62R突变体在表型上与E62K突变体相同,而R78E突变体无法存活。然而,E62R、R78E双突变体不仅能够存活,而且在表型上与单突变体相似。这些结果将TFIIB锌指附近高度保守的序列定义为起始位点选择的关键决定因素,并表明Glu-62-Arg-78盐桥是该结构域的重要结构元件。

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