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一种涉及TFII-I的转录起始替代途径。

An alternative pathway for transcription initiation involving TFII-I.

作者信息

Roy A L, Malik S, Meisterernst M, Roeder R G

机构信息

Laboratory of Biochemistry and Molecular Biology, Rockefeller University, New York, New York 10021-6399.

出版信息

Nature. 1993 Sep 23;365(6444):355-9. doi: 10.1038/365355a0.

Abstract

The minimal promoter elements required for initiation by RNA polymerase II include the TATA box and/or an initiator element (Inr) at or near the transcription start site. Studies of the adenovirus major late core promoter (containing both elements) have demonstrated an initiation pathway that involves binding of the transcription factor TFIID (or the derived subunit, the TATA-binding protein TBP (TFIID tau)) to the TATA element, which is facilitated by transcription factor TFIIA, followed by sequential interactions of other general factors. Here we describe a novel pathway that requires an intact Inr and the Inr-binding factor TFII-I (ref. 3). Sequential addition of the general factors generated TFII-I-dependent preinitiation complexes different from those formed with TFIIA. Furthermore, TBP bound cooperatively (with only TFII-I) to an Inr-containing TATA-less promoter, suggesting a means for activation of TATA-less promoters, which nonetheless require TFIID (refs 9-11). These observations provide support for functionally distinct pathways which could be subject to differential regulation by specific activators or repressors.

摘要

RNA聚合酶II起始转录所需的最小启动子元件包括位于转录起始位点或其附近的TATA盒和/或起始子元件(Inr)。对腺病毒主要晚期核心启动子(包含这两个元件)的研究表明,其起始途径涉及转录因子TFIID(或其衍生亚基,即TATA结合蛋白TBP(TFIID tau))与TATA元件的结合,转录因子TFIIA可促进这种结合,随后其他通用因子依次相互作用。在此,我们描述了一种新的途径,该途径需要完整的Inr和Inr结合因子TFII-I(参考文献3)。通用因子的依次添加产生了与由TFIIA形成的不同的TFII-I依赖性起始前复合物。此外,TBP(仅与TFII-I一起)协同结合到一个不含TATA但含Inr的启动子上,这表明了一种激活不含TATA的启动子的方式,尽管这些启动子仍然需要TFIID(参考文献9 - 11)。这些观察结果为功能上不同的途径提供了支持,这些途径可能受到特定激活剂或抑制剂的差异调节。

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