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通用转录因子TFIIB的序列及其与其他起始因子的关系。

Sequence of general transcription factor TFIIB and relationships to other initiation factors.

作者信息

Malik S, Hisatake K, Sumimoto H, Horikoshi M, Roeder R G

机构信息

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

出版信息

Proc Natl Acad Sci U S A. 1991 Nov 1;88(21):9553-7. doi: 10.1073/pnas.88.21.9553.

Abstract

Transcription factor TFIIB is a ubiquitous factor required for transcription initiation by RNA polymerase II. Previous studies have suggested that TFIIB serves as a bridge between the "TATA"-binding factor (TFIID) and RNA polymerase II during preinitiation complex assembly and, more recently, that TFIIB can be a target of acidic activators. We have purified TFIIB to homogeneity, shown that activity resides in a 33-kDa polypeptide, and obtained cDNAs encoding functional TFIIB. TFIIB contains a region with amino acid sequence similarity to a highly conserved region of prokaryotic sigma factors. This is consistent with analogous functions for these factors in promoter recognition by RNA polymerases and with similar findings for TFIID, TFIIE, and TFIIF/RAP30. Like TFIID, TFIIB contains both a large imperfect repeat that could contribute an element of symmetry to the folded protein and clusters of basic residues that could interact with acidic activator domains. These findings argue for a common origin of TFIIB, TFIID, and other general transcription factors and for the evolutionary segregation of complementary functions.

摘要

转录因子TFIIB是RNA聚合酶II启动转录所必需的一种普遍存在的因子。先前的研究表明,在起始前复合物组装过程中,TFIIB充当“TATA”结合因子(TFIID)与RNA聚合酶II之间的桥梁,并且最近发现TFIIB可能是酸性激活剂的作用靶点。我们已将TFIIB纯化至同质状态,证明其活性存在于一条33 kDa的多肽中,并获得了编码功能性TFIIB的cDNA。TFIIB含有一个区域,其氨基酸序列与原核生物σ因子的一个高度保守区域相似。这与这些因子在RNA聚合酶识别启动子过程中的类似功能以及对TFIID、TFIIE和TFIIF/RAP30的类似发现相一致。与TFIID一样,TFIIB既含有一个可能为折叠后的蛋白质贡献对称元素的大的不完全重复序列,又含有可能与酸性激活结构域相互作用的碱性残基簇。这些发现支持TFIIB、TFIID和其他通用转录因子有共同起源以及互补功能的进化分离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a8/52756/41ad1db5875d/pnas01071-0188-a.jpg

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