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RNA聚合酶II转录的启动子特异性与调控

Promoter specificity and modulation of RNA polymerase II transcription.

作者信息

Saltzman A G, Weinmann R

机构信息

Wistar Institute, Philadelphia, Pennsylvania 19104.

出版信息

FASEB J. 1989 Apr;3(6):1723-33. doi: 10.1096/fasebj.3.6.2649403.

DOI:10.1096/fasebj.3.6.2649403
PMID:2649403
Abstract

RNA polymerase II is a multisubunit enzyme involved in the transcription of protein encoding genes. Recently acquired knowledge of the transcription process and of the RNA polymerase molecule as well as the isolation of subunit clones have led to a better understanding of the enzyme's functional regulation. Specific transcription initiation occurs at promoter regions located upstream of the gene and requires a minimum of five basic factors in addition to the enzyme. Furthermore, proteins that bind to specific DNA elements within the promoter also regulate transcriptional activity. Additional factors are required for the elongation and, possibly, termination of transcription. Two elongation factors, SII and TFIIF, interact directly with the RNA polymerase II molecule. Functional domains of RNA polymerase II have been determined by analysis of genomic clones for the two largest subunits of the enzyme. For example, the 240-kDa largest subunit contains a highly phosphorylated carboxyl-terminal heptapeptide domain repeated 26-52 times that is absolutely required for transcription in vivo. Analysis of the polymerase molecule and its interaction with basic gene-specific transcription factors will aid in our studies of the control of gene expression.

摘要

RNA聚合酶II是一种参与蛋白质编码基因转录的多亚基酶。最近获得的关于转录过程和RNA聚合酶分子的知识,以及亚基克隆的分离,使人们对该酶的功能调节有了更好的理解。特异性转录起始发生在基因上游的启动子区域,除该酶外还至少需要五种基本因子。此外,与启动子内特定DNA元件结合的蛋白质也调节转录活性。转录的延伸和可能的终止还需要其他因子。两种延伸因子SII和TFIIF直接与RNA聚合酶II分子相互作用。RNA聚合酶II的功能结构域已通过对该酶两个最大亚基的基因组克隆分析得以确定。例如,240 kDa的最大亚基包含一个高度磷酸化的羧基末端七肽结构域,重复26 - 52次,这是体内转录绝对必需的。对聚合酶分子及其与基本基因特异性转录因子相互作用的分析将有助于我们对基因表达调控的研究。

相似文献

1
Promoter specificity and modulation of RNA polymerase II transcription.RNA聚合酶II转录的启动子特异性与调控
FASEB J. 1989 Apr;3(6):1723-33. doi: 10.1096/fasebj.3.6.2649403.
2
Transcription elongation factor SII interacts with a domain of the large subunit of human RNA polymerase II.转录延伸因子SII与人RNA聚合酶II大亚基的一个结构域相互作用。
Mol Cell Biol. 1988 Aug;8(8):3136-42. doi: 10.1128/mcb.8.8.3136-3142.1988.
3
Dissection of transcription factor TFIIF functional domains required for initiation and elongation.转录起始和延伸所需转录因子TFIIF功能结构域的剖析。
Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):6042-6. doi: 10.1073/pnas.92.13.6042.
4
Basal components of the transcription apparatus (RNA polymerase II, TATA-binding protein) contain activation domains: is the repetitive C-terminal domain (CTD) of RNA polymerase II a "portable enhancer domain"?转录装置的基础成分(RNA聚合酶II、TATA结合蛋白)包含激活结构域:RNA聚合酶II的重复C末端结构域(CTD)是一个“可移植增强子结构域”吗?
Mol Reprod Dev. 1994 Oct;39(2):215-25. doi: 10.1002/mrd.1080390215.
5
Glutamic acid-371 of the barnase homology domain in RNA polymerase II is not required for SII-activated RNA cleavage.RNA聚合酶II中核糖核酸酶Barnase同源结构域的谷氨酸-371对于SII激活的RNA切割并非必需。
Mol Gen Genet. 1997 Jan 27;253(4):507-11. doi: 10.1007/s004380050350.
6
Gdown1 Associates Efficiently with RNA Polymerase II after Promoter Clearance and Displaces TFIIF during Transcript Elongation.启动子清除后,Gdown1与RNA聚合酶II高效结合,并在转录延伸过程中取代TFIIF。
PLoS One. 2016 Oct 7;11(10):e0163649. doi: 10.1371/journal.pone.0163649. eCollection 2016.
7
Trypanosome spliced leader RNA genes contain the first identified RNA polymerase II gene promoter in these organisms.锥虫剪接前导RNA基因包含这些生物体中首个被鉴定出的RNA聚合酶II基因启动子。
Nucleic Acids Res. 2001 Apr 1;29(7):1556-64. doi: 10.1093/nar/29.7.1556.
8
Homologous domains of the largest subunit of eucaryotic RNA polymerase II are conserved in plants.真核生物RNA聚合酶II最大亚基的同源结构域在植物中是保守的。
Mol Gen Genet. 1990 Aug;223(1):65-75. doi: 10.1007/BF00315798.
9
TFIIF-TAF-RNA polymerase II connection.TFIIF-TAF-核糖核酸聚合酶II连接
Genes Dev. 1994 Dec 1;8(23):2868-78. doi: 10.1101/gad.8.23.2868.
10
The carboxyl-terminal repeat domain of RNA polymerase II is not required for transcription factor Sp1 to function in vitro.转录因子Sp1在体外发挥功能时,RNA聚合酶II的羧基末端重复结构域并非必需。
J Biol Chem. 1990 May 25;265(15):8351-3.

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