Regulation of transcription elongation by phosphorylation

被引:165
作者
Kobor, MS
Greenblatt, J
机构
[1] Univ Toronto, Banting & Best Dept Med Res, Dept Mol & Med Genet, Toronto, ON M5G 1L6, Canada
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2002年 / 1577卷 / 02期
关键词
RNA polymerase II; transcription initiation; transcription elongation; protein kinase; protein phosphatase; HIV Tat;
D O I
10.1016/S0167-4781(02)00457-8
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
The synthesis of mRNA by RNA polymerase II (RNAPII) is a multistep process that is regulated by different mechanisms. One important aspect of transcriptional regulation is phosphorylation of components of the transcription apparatus. The phosphorylation state of RNAPII carboxy-terminal domain (CTD) is controlled by a variety of protein kinases and at least one protein phosphatase. We discuss emerging a and biochemical evidence that points to a role of these factors not only in transcription initiation but also in elongation and possibly genetic, termination. In addition, we review phosporylation events involving some of the general transcription factors (GTFs) and other regulatory proteins. As an interesting example, we describe the modulation of transcription associated kinases and phosphatase by the HIV Tat protein. We focus on bringing together recent Findings and propose a revised model for the RNAPII phosphorylation cycle. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:261 / 275
页数:15
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