RNA聚合酶II控制转录伸长:回顾。

Q3 Biochemistry, Genetics and Molecular Biology Genetics Research International Pub Date : 2012-01-01 Epub Date: 2012-01-29 DOI:10.1155/2012/170173
Kris Brannan, David L Bentley
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引用次数: 14

摘要

我们目前对转录延伸控制的理解起源于在病毒和细胞基因上绘制RNA聚合酶II的开创性实验。这些研究首次揭示了聚合酶分子的惊人过剩,我们现在知道这些聚合酶分子位于多细胞生物中大多数基因的5'端。在转录起始位点附近堆积的pol II反映了一个普遍存在的瓶颈,它在转录延伸开始时限制了延伸。随后的开创性工作确定了保守的蛋白因子,这些蛋白因子通过这一瓶颈积极或消极地控制聚合酶的通量,并对基因表达的控制做出了重大贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Control of Transcriptional Elongation by RNA Polymerase II: A Retrospective.

The origins of our current understanding of control of transcription elongation lie in pioneering experiments that mapped RNA polymerase II on viral and cellular genes. These studies first uncovered the surprising excess of polymerase molecules that we now know to be situated at the at the 5' ends of most genes in multicellular organisms. The pileup of pol II near transcription start sites reflects a ubiquitous bottle-neck that limits elongation right at the start of the transcription elongation. Subsequent seminal work identified conserved protein factors that positively and negatively control the flux of polymerase through this bottle-neck, and make a major contribution to control of gene expression.

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来源期刊
Genetics Research International
Genetics Research International Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.90
自引率
0.00%
发文量
0
期刊介绍: Genetics Research International is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of genetics and genomics. The journal focuses on articles bearing on heredity, biochemistry, and molecular biology, as well as clinical findings.
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