Mechanisms of regulation of RNA polymerase III-dependent transcription by TORC1

被引:128
作者
Wei, Yuehua [1 ,2 ]
Tsang, Chi Kwan [1 ]
Zheng, X. F. Steven [1 ]
机构
[1] UMDNJ, Dept Pharmacol, Canc Inst New Jersey, Robert Wood Johnson Med Sch, Piscataway, NJ 08854 USA
[2] UMDNJ, Grad Program Cellular & Mol Pharmacol, Robert Wood Johnson Med Sch, Piscataway, NJ USA
关键词
Maf1; nucleolus; rDNA; RNA polymerase III; target of rapamycin (TOR); NUCLEAR-LOCALIZATION; MAMMALIAN TARGET; NEGATIVE REGULATOR; SIGNALING PATHWAYS; RAPAMYCIN; PROTEIN; MAF1; RIBOSOME; REPRESSION; GROWTH;
D O I
10.1038/emboj.2009.179
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
We have found earlier that Tor1 binds to 5S rDNA chromatin but the functional significance has not been established. Here, we show that association with 5S rDNA chromatin is necessary for TOR complex 1 (TORC1) to regulate the synthesis of 5S ribosomal RNA and transfer RNAs (tRNAs) by RNA polymerase (Pol) III, as well as the phosphorylation and binding to Pol III-transcribed genes of the Pol III repressor Maf1. Interestingly, TORC1 does not bind to tRNA genes, suggesting that TORC1 modulates tRNA synthesis indirectly through Maf1 phosphorylation at the rDNA loci. We also find that Maf1 cytoplasmic localization is dependent on the SSD1-v allele. In W303 cells that carry the SSD1-d allele, Maf1 is constitutively nuclear but its nucleolar localization is inhibited by TORC1, indicating that TORC1 regulates nucleoplasm-tonucleolus transport of Maf1. Finally, we show that TORC1 interacts with Maf1 in vivo and phosphorylates Maf1 in vitro, and regulates Maf1 nucleoplasm-to-nucleolus translocation. Together, these observations provide new insights into the chromatin-dependent mechanism by which TORC1 controls transcription by Pol III. The EMBO Journal (2009) 28, 2220-2230. doi:10.1038/emboj.2009.179; Published online 2 July 2009
引用
收藏
页码:2220 / 2230
页数:11
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