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高等真核生物RNA聚合酶B启动子的转录元件和因子

Transcription elements and factors of RNA polymerase B promoters of higher eukaryotes.

作者信息

Wasylyk B

机构信息

Laboratoire de Genetique Moleculaire des Eucaryotes du CNRS, Strasbourg, France.

出版信息

CRC Crit Rev Biochem. 1988;23(2):77-120. doi: 10.3109/10409238809088317.

Abstract

The promoter for eukaryotic genes transcribed by RNA polymerase B can be divided into the TATA box (located at -30) and startsite (+1), the upstream element (situated between -40 and about -110), and the enhancer (no fixed position relative to the startsite). Trans-acting factors, which bind to these elements, have been identified and at least partially purified. The role of the TATA box is to bind factors which focus the transcription machinery to initiate at the startsite. The upstream element and the enhancer somehow modulate this interaction, possibly through direct protein-protein interactions. Another class of transcription factors, typified by viral proteins such as the adenovirus EIA products, do not appear to require binding to a particular DNA sequence to regulate transcription. The latest findings in these various subjects are discussed.

摘要

由RNA聚合酶B转录的真核基因启动子可分为位于-30处的TATA框和起始位点(+1)、上游元件(位于-40至约-110之间)以及增强子(相对于起始位点无固定位置)。已鉴定出并至少部分纯化了与这些元件结合的反式作用因子。TATA框的作用是结合一些因子,这些因子将转录机制集中在起始位点启动转录。上游元件和增强子可能通过直接的蛋白质-蛋白质相互作用,以某种方式调节这种相互作用。另一类转录因子,以腺病毒EIA产物等病毒蛋白为代表,似乎不需要与特定的DNA序列结合来调节转录。本文讨论了这些不同主题的最新研究结果。

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