RNA polymerase III transcription repressed by Rb through its interactions with TFIIIB and TFIIIC2

被引:59
作者
Chu, WM
Wang, ZX
Roeder, RG
Schmid, CW
机构
[1] UNIV CALIF DAVIS, SECT MOL & CELLULAR BIOL, DAVIS, CA 95616 USA
[2] ROCKEFELLER UNIV, BIOCHEM & MOL BIOL LAB, NEW YORK, NY 10021 USA
[3] UNIV CALIF DAVIS, DEPT CHEM, DAVIS, CA 95616 USA
关键词
D O I
10.1074/jbc.272.23.14755
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 retinoblastoma susceptibility gene product (Rb) generally represses RNA polymerase III (Pol III)-directed transcription. This implies that Rb interacts with essential transcription factors. Mutations in either the A or B subdomains in the Rb pocket interfere with Rb-mediated repression of Pol III-directed transcription, which indicates that both subdomains are directly involved in this activity. Addition of either purified TFIIIB or purified TFIIIC2 partially relieves Rb-mediated repression and restores activity to nuclear extracts that had been depleted of essential factors by binding to Rb. Pull down and coimmunoprecipitation experiments as web as functional assays indicate that Rb interacts with both TFIIIB and TFIIIC2 and that the A subdomain is primarily required for binding TFIIIB and the B subdomain for binding TFIIIC2. While Rb interacts with both factors, the A subdomain is more important than the B subdomain in directing Rb-mediated repression, and TFIIIB is the principal target of that activity.
引用
收藏
页码:14755 / 14761
页数:7
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