The regulatory role for the ERCC3 helicase of general transcription factor TFIIH during promoter escape in transcriptional activation

被引:18
作者
Fukuda, A [1 ]
Nogi, Y [1 ]
Hisatake, K [1 ]
机构
[1] Saitama Med Sch, Dept Mol Biol, Moroyama, Saitama 3500495, Japan
关键词
D O I
10.1073/pnas.251674198
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
Eukaryotic transcriptional activators have been proposed to function, for the most part, by promoting the assembly of preinitiation complex through the recruitment of the RNA polymerase II transcriptional machinery to the promoter. Previous studies have shown that transcriptional activation is critically dependent on transcription factor IIH (TFIIH), which functions during promoter opening and promoter escape, the steps following preinitiation complex assembly. Here we have analyzed the role of TFIIH in transcriptional activation and show that the excision repair cross-complementing (ERCC) 3 helicase activity of TFIIH plays a regulatory role to stimulate promoter escape in activated transcription, The stimulatory effect of the ERCC3 helicase is observed until approximate to10-nt RNA is synthesized, and the helicase seems to act throughout the entire course of promoter escape, Analyses of the early phase of transcription show that a majority of the initiated complexes abort transcription and fail to escape the promoter; however, the proportion of productive complexes that escape the promoter apparently increases in response to activation. Our results establish that promoter escape is an important regulatory step stimulated by the ERCC3 helicase activity in response to activation and reveal a possible mechanism of transcriptional synergy.
引用
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页码:1206 / 1211
页数:6
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