Protein kinase A regulates RNA polymerase III transcription through the nuclear localization of Maf1

被引:112
作者
Moir, Robyn D.
Lee, JaeHoon
Haeusler, Rebecca A.
Desai, Neelam
Engelke, David R.
Willis, Ian M.
机构
[1] Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10461 USA
[2] Univ Michigan, Sch Med, Dept Biol Chem, Ann Arbor, MI 48109 USA
关键词
nuclear import; phosphorylation; tRNA biosynthesis;
D O I
10.1073/pnas.0607129103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Maf1 is an essential and specific mediator of transcriptional repression in the RNA polymerase (pol) III system. Maf1-dependent repression occurs in response to a wide range of conditions, suggesting that the protein itself is targeted by the major nutritional and stress-signaling pathways. We show that Maf1 is a substrate for cAMP-dependent PKA in vitro and is differentially phosphorylated on PKA sites in vivo under normal versus repressing conditions. PKA activity negatively regulates Maf1 function because strains with unregulated high PKA activity block repression of pol III transcription in vivo, and strains lacking all PKA activity are hyperrepressible. Nuclear accumulation of Maf1 is required for transcriptional repression and is regulated by two nuclear localization sequences in the protein. An analysis of PKA phosphosite mutants shows that the localization of Maf1 is affected via the N-terminal nuclear localization sequence. In particular, mutations that prevent phosphorylation at PKA consensus sites promote nuclear accumulation of Maf1 without inducing repression. These results indicate that negative regulation of Maf1 by PKA is achieved by inhibiting its nuclear import and suggest that a PKA-independent activation step is required for nuclear Maf1 to function in the repression of pol III transcription. Finally, we report a previously undescribed phenotype for Maf1 in tRNA gene-mediated silencing of nearby RNA pol II transcription.
引用
收藏
页码:15044 / 15049
页数:6
相关论文
共 32 条
[1]   Nucleolar localization of early tRNA processing [J].
Bertrand, E ;
Houser-Scott, F ;
Kendall, A ;
Singer, RH ;
Engelke, DR .
GENES & DEVELOPMENT, 1998, 12 (16) :2463-2468
[2]   Mutation in a new gene MAF1 affects tRNA suppressor efficiency in Saccharomyces cerevisiae [J].
Boguta, M ;
Czerska, K ;
Zoladek, T .
GENE, 1997, 185 (02) :291-296
[3]   An evolutionary proteomics approach identifies substrates of the cAMP-dependent protein kinase [J].
Budovskaya, YV ;
Stephan, JS ;
Deminoff, SJ ;
Herman, PK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) :13933-13938
[4]   CAMP-INDEPENDENT CONTROL OF SPORULATION, GLYCOGEN-METABOLISM, AND HEAT-SHOCK RESISTANCE IN S-CEREVISIAE [J].
CAMERON, S ;
LEVIN, L ;
ZOLLER, M ;
WIGLER, M .
CELL, 1988, 53 (04) :555-566
[5]   Two steps in Maf1-dependent repression of transcription by RNA polymerase III [J].
Desai, N ;
Lee, JH ;
Upadhya, R ;
Chu, Y ;
Moir, RD ;
Willis, IM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (08) :6455-6462
[6]   THE SACCHAROMYCES-CEREVISIAE YAK1-GENE ENCODES A PROTEIN-KINASE THAT IS INDUCED BY ARREST EARLY IN THE CELL-CYCLE [J].
GARRETT, S ;
MENOLD, MM ;
BROACH, JR .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (08) :4045-4052
[7]   Genome-wide location of yeast RNA polymerase III transcription machinery [J].
Harismendy, O ;
Gendrel, CG ;
Soularue, P ;
Gidrol, X ;
Sentenac, A ;
Werner, M ;
Lefebvre, O .
EMBO JOURNAL, 2003, 22 (18) :4738-4747
[8]   Regulation of nuclear import by phosphorylation adjacent to nuclear localization signals [J].
Harreman, MT ;
Kline, TM ;
Milford, HG ;
Harben, MB ;
Hodel, AE ;
Corbett, AH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (20) :20613-20621
[9]   The oncogenic RAS2val19 mutation locks respiration, independently of PKA, in a mode prone to generate ROS [J].
Hlavatá, L ;
Aguilaniu, H ;
Pichová, A ;
Nyström, T .
EMBO JOURNAL, 2003, 22 (13) :3337-3345
[10]   TRANSFER-RNA GENES AS TRANSCRIPTIONAL REPRESSOR ELEMENTS [J].
HULL, MW ;
ERICKSON, J ;
JOHNSTON, M ;
ENGELKE, DR .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (02) :1266-1277