RNA-POLYMERASE - REGULATION OF TRANSCRIPT ELONGATION AND TERMINATION

被引:130
作者
KERPPOLA, TK [1 ]
KANE, CM [1 ]
机构
[1] UNIV CALIF BERKELEY,DIV BIOCHEM & MOLEC BIOL,401 BARKER HALL,BERKELEY,CA 94720
关键词
GENE REGULATION; ATTENUATION; ANTITERMINATION;
D O I
10.1096/fasebj.5.13.1916107
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
Expanded interest in studying the mechanisms of elongation and termination during transcription has come as a result of several recent findings that highlight the importance of the regulation of these processes in human health. Several cellular proto-oncogenes contain regulated blocks to elongation (1), and the human immunodeficiency viruses also control gene expression in part by regulating the efficiency of elongation in response to the trans-activating protein, TAT (2). This review considers these recent findings and compares potential mechanisms of regulation used by prokaryotic and eukaryotic RNA polymerases during elongation and termination. In all these systems, many of the detailed mechanisms of transcription elongation and termination are still to be defined; however, we have tried to group examples that may share some common regulatory elements into simplified categories.
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页码:2833 / 2842
页数:10
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