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从一个非典型的、含TATATAA框的管家启动子起始转录所需的最小序列和因子要求。

Minimal sequence and factor requirements for the initiation of transcription from an atypical, TATATAA box-containing housekeeping promoter.

作者信息

Boyer T G, Maquat L E

机构信息

Department of Human Genetics, Roswell Park Cancer Institute, New York State Department of Health, Buffalo 14263.

出版信息

J Biol Chem. 1990 Nov 25;265(33):20524-32.

PMID:2243103
Abstract

We have established the minimal sequence and factor requirements for both constitutive and viral-induced transcription from an atypical, TATATAA box-containing human housekeeping promoter. Utilizing a transient cotransfection protocol, we have found that efficient transactivation of triosephosphate isomerase (TPI) gene transcription by the immediate early proteins of adenovirus and pseudorabies virus is dependent upon the same assembly of sequence elements that collectively confer minimal TPI promoter function in the absence of viral protein. These elements span TPI promoter positions -65 and -6 (where +1 is the transcription initiation site) and include not only a TFIID-responsive TATATAA box (-27 to -21) but a single GC box (-53 to -48) that binds Spl, and a novel cap proximal element (-18 to -6) that binds a 110-kDa nuclear factor that is present in HeLa cells. We demonstrate that these elements function in an interdependent fashion; deleting either GC box 1 or the cap proximal element completely or nearly abolished both basal transcription and viral transactivation. Therefore, these elements and their cognate factors represent the basal transcription initiation complex through which the immediate early protein of adenovirus or pseudorabies virus mediates the stimulation of TPI gene transcription. We discuss the implications of these data for both constitutive and viral-induced transcription.

摘要

我们已经确定了来自一个非典型的、含TATATAA框的人类管家启动子的组成型和病毒诱导转录的最小序列和因子要求。利用瞬时共转染方案,我们发现腺病毒和伪狂犬病病毒的立即早期蛋白对磷酸丙糖异构酶(TPI)基因转录的有效反式激活依赖于在没有病毒蛋白时共同赋予最小TPI启动子功能的相同序列元件组装。这些元件跨越TPI启动子的-65至-6位置(其中+1为转录起始位点),不仅包括一个TFIID反应性TATATAA框(-27至-21),还包括一个结合Spl的单一GC框(-53至-48),以及一个结合HeLa细胞中存在的110 kDa核因子的新型帽近端元件(-18至-6)。我们证明这些元件以相互依赖的方式发挥作用;完全删除GC框1或帽近端元件会完全或几乎消除基础转录和病毒反式激活。因此,这些元件及其同源因子代表了基础转录起始复合物,腺病毒或伪狂犬病病毒的立即早期蛋白通过该复合物介导对TPI基因转录的刺激。我们讨论了这些数据对组成型和病毒诱导转录的意义。

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