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裂殖酵母中RNA聚合酶II的转录终止信号

Transcriptional termination signals for RNA polymerase II in fission yeast.

作者信息

Birse C E, Lee B A, Hansen K, Proudfoot N J

机构信息

Sir William Dunn School of Pathology, Chemical Pathology Unit, University of Oxford, UK.

出版信息

EMBO J. 1997 Jun 16;16(12):3633-43. doi: 10.1093/emboj/16.12.3633.

Abstract

Transcription 'run-on' (TRO) analysis using permeabilized yeast cells indicates that transcription terminates between 180 and 380 bp downstream of the poly(A) site of the Schizosaccharomyces pombe ura4 gene. Two signals direct RNA polymerase II (pol II) to stop transcription: the previously identified 3' end formation signals located close to the poly(A) site and an additional downstream element (DSE) located at the region of termination. The downstream signal (135 bp) appears to act by pausing the elongating polymerase. TRO analysis indicates that elevated levels of transcribing polymerases accumulate over the DSE and that removal of this signal leads to transcription proceeding beyond the normal termination region. Furthermore, when inserted between two competing polyadenylation signals, this DSE increases the utilization of upstream poly(A) sites in vivo. We show that polymerase pausing over an extended region of template ensures termination of pol II transcription close to the poly(A) site.

摘要

使用通透化酵母细胞进行的转录“通读”(TRO)分析表明,转录在粟酒裂殖酵母ura4基因poly(A)位点下游180至380 bp之间终止。有两个信号引导RNA聚合酶II(pol II)停止转录:先前确定的位于poly(A)位点附近的3'端形成信号,以及位于终止区域的另一个下游元件(DSE)。下游信号(135 bp)似乎通过使延伸中的聚合酶暂停起作用。TRO分析表明,转录聚合酶水平升高在DSE上积累,去除该信号会导致转录超出正常终止区域继续进行。此外,当插入两个相互竞争的聚腺苷酸化信号之间时,该DSE会增加体内上游poly(A)位点的利用率。我们表明,聚合酶在模板的延伸区域上暂停可确保pol II转录在poly(A)位点附近终止。

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