Pol II waiting in the starting gates: Regulating the transition from transcription initiation into productive elongation

被引:199
作者
Nechaev, Sergei [1 ]
Adelman, Karen [1 ]
机构
[1] NIEHS, Mol Carcinogenesis Lab, NIH, Res Triangle Pk, NC 27709 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2011年 / 1809卷 / 01期
关键词
RNA polymerase II; Gene regulation; Transcription elongation; Polymerase pausing; RNA-POLYMERASE-II; HEAT-SHOCK GENES; BROMODOMAIN PROTEIN BRD4; CARBOXYL-TERMINAL DOMAIN; MAJOR LATE PROMOTER; P-TEFB; DROSOPHILA-MELANOGASTER; IN-VIVO; C-MYC; CAPPING ENZYME;
D O I
10.1016/j.bbagrm.2010.11.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proper regulation of gene expression is essential for the differentiation, development and survival of all cells and organisms. Recent work demonstrates that transcription of many genes, including key developmental and stimulus-responsive genes, is regulated after the initiation step, by pausing of RNA polymerase II during elongation through the promoter-proximal region. Thus, there is great interest in better understanding the events that follow transcription initiation and the ways in which the efficiency of early elongation can be modulated to impact expression of these highly regulated genes. Here we describe our current understanding of the steps involved in the transition from an unstable initially transcribing complex into a highly stable and processive elongation complex. We also discuss the interplay between factors that affect early transcript elongation and the potential physiological consequences for genes that are regulated through transcriptional pausing. Published by Elsevier B.V.
引用
收藏
页码:34 / 45
页数:12
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