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TBP 结合与人类β-珠蛋白基因转录起始速率

TBP binding and the rate of transcription initiation from the human beta-globin gene.

作者信息

Antoniou M, de Boer E, Spanopoulou E, Imam A, Grosveld F

机构信息

Laboratory of Gene Structure and Expression, National Institute for Medical Research, London, UK.

出版信息

Nucleic Acids Res. 1995 Sep 11;23(17):3473-80. doi: 10.1093/nar/23.17.3473.

Abstract

DNA-protein interaction studies in vitro revealed several factors binding over the TATA box and the region of transcription initiation (cap) site of the human beta-globin promoter; TATA binding protein TBP at -30, Sp1 at -19, GATA-1 at -12 and +5, YY1 at -9 and a novel factor C1 over the site of initiation (-4 to +7). Point mutants which specifically abolish the binding of each of these proteins were tested in a beta-globin locus control region (LCR) construct which allows quantitative comparisons at physiological levels of transcription. Only mutants which drastically affect the binding of TBP resulted in decreased levels of transcription. A threshold value of TBP binding of 15-30% of wild type was sufficient to give normal levels of transcription. This indicates that the association of TF IID with the TATA box is not limiting in the rate of initiation of transcription.

摘要

体外DNA-蛋白质相互作用研究揭示了几种结合于人β-珠蛋白启动子TATA盒及转录起始(帽)位点区域的因子;-30位的TATA结合蛋白TBP、-19位的Sp1、-12位和+5位的GATA-1、-9位的YY1以及起始位点(-4至+7)上的一种新因子C1。在一个β-珠蛋白基因座控制区(LCR)构建体中测试了特异性消除这些蛋白质各自结合的点突变体,该构建体允许在生理转录水平进行定量比较。只有那些严重影响TBP结合的突变体导致转录水平降低。TBP结合达到野生型的15%-30%的阈值就足以产生正常水平的转录。这表明TF IID与TATA盒的结合在转录起始速率方面并非限制因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a38c/307226/e9b8effefb02/nar00017-0123-a.jpg

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