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RNA聚合酶II通用转录机制的分子遗传学

Molecular genetics of the RNA polymerase II general transcriptional machinery.

作者信息

Hampsey M

机构信息

Department of Biochemistry, Division of Nucleic Acids Enzymology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey 08854-5635, USA.

出版信息

Microbiol Mol Biol Rev. 1998 Jun;62(2):465-503. doi: 10.1128/MMBR.62.2.465-503.1998.

Abstract

Transcription initiation by RNA polymerase II (RNA pol II) requires interaction between cis-acting promoter elements and trans-acting factors. The eukaryotic promoter consists of core elements, which include the TATA box and other DNA sequences that define transcription start sites, and regulatory elements, which either enhance or repress transcription in a gene-specific manner. The core promoter is the site for assembly of the transcription preinitiation complex, which includes RNA pol II and the general transcription fctors TBP, TFIIB, TFIIE, TFIIF, and TFIIH. Regulatory elements bind gene-specific factors, which affect the rate of transcription by interacting, either directly or indirectly, with components of the general transcriptional machinery. A third class of transcription factors, termed coactivators, is not required for basal transcription in vitro but often mediates activation by a broad spectrum of activators. Accordingly, coactivators are neither gene-specific nor general transcription factors, although gene-specific coactivators have been described in metazoan systems. Transcriptional repressors include both gene-specific and general factors. Similar to coactivators, general transcriptional repressors affect the expression of a broad spectrum of genes yet do not repress all genes. General repressors either act through the core transcriptional machinery or are histone related and presumably affect chromatin function. This review focuses on the global effectors of RNA polymerase II transcription in yeast, including the general transcription factors, the coactivators, and the general repressors. Emphasis is placed on the role that yeast genetics has played in identifying these factors and their associated functions.

摘要

RNA聚合酶II(RNA pol II)引发转录需要顺式作用启动子元件与反式作用因子之间相互作用。真核生物启动子由核心元件和调控元件组成,核心元件包括TATA框和其他确定转录起始位点的DNA序列,调控元件则以基因特异性方式增强或抑制转录。核心启动子是转录前起始复合物组装的位点,该复合物包括RNA pol II以及通用转录因子TBP、TFIIB、TFIIE、TFIIF和TFIIH。调控元件结合基因特异性因子,这些因子通过直接或间接与通用转录机制的组分相互作用来影响转录速率。第三类转录因子称为共激活因子,体外基础转录不需要它们,但它们常常介导多种激活因子的激活作用。因此,共激活因子既不是基因特异性的也不是通用转录因子,尽管后生动物系统中已描述了基因特异性共激活因子。转录抑制因子包括基因特异性因子和通用因子。与共激活因子类似,通用转录抑制因子影响多种基因的表达,但并不抑制所有基因。通用抑制因子要么通过核心转录机制起作用,要么与组蛋白相关,大概影响染色质功能。本综述着重于酵母中RNA聚合酶II转录的全局效应物,包括通用转录因子、共激活因子和通用抑制因子。重点在于酵母遗传学在鉴定这些因子及其相关功能中所起的作用。

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