The regulation of elongation by eukaryotic RNA polymerase II: A recent view

被引:0
|
作者
Kim, D
Yamaguchi, Y
Wada, T
Handa, H [1 ]
机构
[1] Frontier Collaborat Res Ctr, Yokohama, Kanagawa 2268501, Japan
[2] Tokyo Inst Technol, Grad Sch Biosci & Biotechnol, Yokohama, Kanagawa 2268501, Japan
关键词
DRB; DSIF (hSpt4/hSpt5); elongation; NELF;
D O I
暂无
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 elongation of mRNA by RNA polymerase II (RNAPII) is controlled by the diverse actions of cis- and trans-acting elements that respond to a variety of biological signals. Elongation regulation, which determines the processivity of RNAPII, occurs during the steps of transcription initiation and elongation through both negative and positive influences. It has been generally accepted that negative elongation factors repress the elongation reaction. It is also generally accepted that positive elongation factors act by allowing the stalled RNAPII to escape from an inactive state, thus facilitating the production of full-length transcripts. However, recent data suggests that these opposing regulatory mechanisms can be achieved through a coupling pattern, rather than through independent activity. In addition, biochemical experiments using 5,6-<(d)underbar>ichloro-1-beta -D-(r) under bar ibofuranosyl (b) under bar enzimidazole (DRB) have identified several factors involved in DRB-sensitive transcription, and elucidated the me chanism of interplay between the positive and negative elongation factors. Here, we will review the major findings from studies on RNAPII elongation control. We will further discuss the properties of newly identified factors that have resulted from studies on the action of DRB on elongation.
引用
收藏
页码:267 / 274
页数:8
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