The Rpb6 subunit of fission yeast RNA polymerase II is a contact target of the transcription elongation factor TFIIS

被引:31
作者
Ishiguro, A
Nogi, Y
Hisatake, K
Muramatsu, M
Ishihama, A [1 ]
机构
[1] Natl Inst Genet, Dept Mol Genet, Shizuoka 4118540, Japan
[2] Grad Univ Adv Studies, Sch Life Sci, Shizuoka 4118540, Japan
[3] Saitama Med Sch, Dept Biochem, Moroyama, Saitama 3500095, Japan
关键词
D O I
10.1128/MCB.20.4.1263-1270.2000
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Rpb6 subunit of RNA polymerase II is one of the five subunits common to three forms of eukaryotic RNA polymerase. Deletion and truncation analyses of the rpb6 gene in the fission yeast Schizosaccharomyces pombe indicated that Rpb6, consisting of 142 amino acid residues, is an essential protein for cell viability, and the essential region is located in the C-terminal half between residues 61 and 139. After random mutagenesis, a total of 14 temperature-sensitive mutants were isolated, each carrying a single (or double in three cases and triple in one) mutation. Four mutants each carrying a single mutation in the essential region mere sensitive to 6-azauracil (6AU), which inhibits transcription elongation by depleting the intracellular pool of GTP and UTP. Both 6AU sensitivity and temperature-sensitive phenotypes of these rpb6 mutants were suppressed by overexpression of TFIIS, a transcription elongation factor. In agreement with the genetic studies, the mutant RNA polymerases containing the mutant Rpb6 subunits showed reduced affinity for TFIIS, as measured by a pull-down assay of TFIIS-RNA polymerase II complexes using a fusion form of TFIIS with glutathione S-transferase. Moreover, the direct interaction between TFIIS and RNA polymerase II was competed by the addition of Rpb6. Taken together, the results lead us to propose that Rpb6 plays a role in the interaction between RNA polymerase II and the transcription elongation factor TFIIS.
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页码:1263 / 1270
页数:8
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