RNA-POLYMERASE-II C-TERMINAL DOMAIN REQUIRED FOR ENHANCER-DRIVEN TRANSCRIPTION

被引:144
|
作者
GERBER, HP
HAGMANN, M
SEIPEL, K
GEORGIEV, O
WEST, MAL
LITINGTUNG, Y
SCHAFFNER, W
CORDEN, JL
机构
[1] UNIV CALIF DAVIS,DIV BIOL SCI,PLANT BIOL SECT,DAVIS,CA 95616
[2] JOHNS HOPKINS UNIV,SCH MED,HOWARD HUGHES MED INST,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT MOLEC BIOL & GENET,BALTIMORE,MD 21205
关键词
D O I
10.1038/374660a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
THE RNA polymerase II carboxy-terminal domain (CTD) consists of tandem repeats of the sequence Tyr-Ser-Pro-Thr-Ser-Pro-Ser(1-3). The CTD may participate in activated transcription through interaction with a high-molecular-weight mediator complex(4-6). Such a role would be consistent with observations that some genes are preferentially sensitive to CTD mutations(7,8). Here we investigate the function of the mouse RNA polymerase CTD in enhancer-driven transcription. Transcription by alpha-amanitin-resistant CTD-deletion mutants was tested by transient transfection of tissue culture cells in the presence of alpha-amanitin in order to inhibit endogenous RNA polymerase II. Removal of most of the CTD abolishes transcriptional activation by all enhancers tested, whereas transcription from promoters driven by Sp1, a factor that typically activates housekeeping genes from positions proximal to the initiation sites, is not affected. These findings show that the CTD is essential in mediating 'enhancer'-type activation of mammalian transcription.
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页码:660 / 662
页数:3
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