Stimulation of RNA polymerase II transcript cleavage activity contributes to maintain transcriptional fidelity in yeast

被引:45
|
作者
Koyama, Hiroshi
Ito, Takahiro
Nakanishi, Toshiyuki
Sekimizu, Kazuhisa
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Microbiol, Bunkyo Ku, Tokyo 1130033, Japan
[2] Daiichi Pharmaceut Co Ltd, Tokyo R&D Ctr, New Prod Res Labs 3, Tokyo, Japan
关键词
D O I
10.1111/j.1365-2443.2007.01072.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The transcription elongation factor S-II, also designated TFIIS, stimulates the nascent transcript cleavage activity intrinsic to RNA polymerase II. Rpb9, a small subunit of RNA polymerase II, enhances the cleavage stimulation activity of S-II. Here, we investigated the role of nascent transcript cleavage stimulation activity on the maintenance of transcriptional fidelity in yeast. In yeast, S-II is encoded by the DST1 gene. Disruption of the DST1 gene decreased transcriptional fidelity in cells. Mutations in the DST1 gene that reduce the S-II cleavage stimulation activity led to decreased transcriptional fidelity in cells. A disruption mutant of the RPB9 gene also had decreased transcriptional fidelity. Expression of mutant Rpb9 proteins that are unable to enhance the S-II cleavage stimulation activity failed to restore the phenotype. These results suggest that both S-II and Rpb9 maintain transcriptional fidelity by stimulating the cleavage activity intrinsic to RNA polymerase II. Also, a DST1 and RPB9 double mutant had more severe transcriptional fidelity defect compared with the DST1 gene deletion mutant, suggesting that Rpb9 maintains transcriptional fidelity via two mechanisms, enhancement of S-II dependent cleavage stimulation and S-II independent function(s).
引用
收藏
页码:547 / 559
页数:13
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