Regulation of RNA polymerase III transcription by Maf1 in mammalian cells

被引:50
作者
Goodfellow, Sarah J. [2 ]
Graham, Emma L. [2 ]
Kantidakis, Theodoros [1 ,2 ]
Marshall, Lynne [1 ,2 ]
Coppins, Beverly A. [2 ]
Oficjalska-Pham, Danuta [3 ,4 ]
Gerard, Matthieu [5 ]
Lefebvre, Olivier [3 ]
White, Robert J. [1 ,2 ]
机构
[1] Beatson Inst Canc Res, Glasgow G61 1BD, Lanark, Scotland
[2] Univ Glasgow, Inst Biomed & Life Sci, Div Biochem & Mol Biol, Glasgow G12 8QQ, Lanark, Scotland
[3] CEA, Serv Biochim & Genet Mol, Lab Transcript Genes, F-91191 Gif Sur Yvette, France
[4] Polish Acad Sci, Inst Biochem & Biophys, Dept Genet, PL-02106 Warsaw, Poland
[5] CEA Saclay, Serv Biol Mol, Lab Transgenese, F-91191 Gif Sur Yvette, France
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Maf1; RNA polymerase III; TFIIIB; transcription;
D O I
10.1016/j.jmb.2008.02.060
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
RNA polymerase (pol) III produces essential components of the biosynthetic machinery; therefore, its output is tightly coupled with the rate of cell growth and proliferation. In Saccharomyces cerevisiae, Maf1 is an essential mediator of pol III repression in response to starvation. We demonstrate that a Maf1 ortholog is also used to restrain pol III activity in mouse and human cells. Mammalian Maf1 represses pol III transcription in vitro and in transfected fibroblasts. Furthermore, genetic deletion of Maf1 elevates pol III transcript expression, thus confirming the role of endogenous Maf1 as an inhibitor of mammalian pol III output. Maf1 is detected at chromosomal pol III templates in rodent and human cells. It interacts with pol III as well as its associated initiation factor TFIIIB and is phosphorylated in a serum-sensitive manner in vivo. These aspects of Maf1 function have been conserved between yeast and mammals and are therefore likely to be of fundamental importance in controlling pol III transcriptional activity. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:481 / 491
页数:11
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