Direct Regulation of RNA Polymerase III Transcription by RB, p53 and c-Myc

被引:101
作者
Felton-Edkins, Zoe A. [1 ]
Kenneth, Niall S. [1 ]
Brown, Timothy R. P. [1 ]
Daly, Nicole L. [1 ]
Gomez-Roman, Natividad [1 ]
Grandori, Carla [2 ]
Eisenman, Robert N. [2 ]
White, Robert J. [1 ]
机构
[1] Univ Glasgow, Div Biochem & Mol Biol, Inst Biomed & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
[2] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
关键词
c-Myc; Growth; p53; RB; RNA polymerase III; TFIIIB; transcription; tRNA;
D O I
10.4161/cc.2.3.375
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The synthesis of tRNA and 5S rRNA by RNA polymerase (pol) III is cell cycle regulated in higher organisms. Overexpression of pol III products is a general feature of transformed cells. These observations may be explained by the fact that a pol III-specific transcription factor, TFIIIB, is strongly regulated by the tumor suppressors RB and p53, as well as the proto-oncogene product c-Myc. RB and p53 repress TFIIIB, but this restraint can be lost in tumors through a variety of mechanisms. In contrast, c-Myc binds and activates TFIIIB, causing potent induction of pol III transcription. Using chromatin immunoprecipitation and RNA interference, we show that c-Myc interacts with tRNA and 5S rRNA genes in transformed cervical cells, stimulating their expression. Availability of pol III products may be an important determinant of a cell's capacity to grow. The ability to regulate pol III output may therefore be integral to the growth control functions of RB, p53 and c-Myc.
引用
收藏
页码:181 / 184
页数:4
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