Cell growth- and differentiation-dependent regulation of RNA polymerase III transcription

References

• Roeder RG, Rutter WJ. Multiple forms of DNA-dependent RNA polymerase in eukaryotic organisms. Nature 1969; 224:234 - 237
   PubMed Web of Science ®Google Scholar
• Ream TS, Haag JR, Wierzbicki AT, Nicora CD, Norbeck AD, Zhu JK, et al. Subunit compositions of the RNA-silencing enzymes Pol IV and Pol V reveal their origins as specialized forms of RNA polymerase II. Mol Cell 2009; 33:192 - 203
   PubMed Web of Science ®Google Scholar
• Wierzbicki AT, Haag JR, Pikaard CS. Noncoding transcription by RNA polymerase Pol IVb/Pol V mediates transcriptional silencing of overlapping and adjacent genes. Cell 2008; 135:635 - 648
   PubMed Web of Science ®Google Scholar
• Haurie V, Durrieu-Gaillard S, Dumay-Odelot H, Da Silva D, Rey C, Prochazkova M, et al. Two isoforms of human RNA polymerase III with specific functions in cell growth and transformation. Proc Natl Acad Sci USA 2010; 107:4176 - 4181
   PubMed Web of Science ®Google Scholar
• Dieci G, Fiorino G, Castelnuovo M, Teichmann M, Pagano A. The expanding RNA polymerase III transcriptome. Trends Genet 2007; 23:614 - 622
   PubMed Web of Science ®Google Scholar
• Huang Y, Maraia RJ. Comparison of the RNA polymerase III transcription machinery in Schizosaccharomyces pombe, Saccharomyces cerevisiae and human. Nucleic Acids Res 2001; 29:2675 - 2690
   PubMed Web of Science ®Google Scholar
• Dumay-Odelot H, Marck C, Durrieu-Gaillard S, Lefebvre O, Jourdain S, Prochazkova M, et al. Identification, molecular cloning and characterization of the sixth subunit of human transcription factor TFIIIC. J Biol Chem 2007; 282:17179 - 17189
   PubMed Web of Science ®Google Scholar
• Engelke DR, Ng SY, Shastry BS, Roeder RG. Specific interaction of a purified transcription factor with an internal control region of 5S RNA genes. Cell 1980; 19:717 - 728
   PubMed Web of Science ®Google Scholar
• Geiduschek EP, Kassavetis GA. The RNA polymerase III transcription apparatus. J Mol Biol 2001; 310:1 - 26
   PubMed Web of Science ®Google Scholar
• Waldschmidt R, Wanandi I, Seifart KH. Identification of transcription factors required for the expression of mammalian U6 genes in vitro. EMBO J 1991; 10:2595 - 2603
   PubMed Web of Science ®Google Scholar
• Murphy S, Yoon JB, Gerster T, Roeder RG. Oct-1 and Oct-2 potentiate functional interactions of a transcription factor with the proximal sequence element of small nuclear RNA genes. Mol Cell Biol 1992; 12:3247 - 3261
   PubMed Web of Science ®Google Scholar
• Sadowski CL, Henry RW, Lobo SM, Hernandez N. Targeting TBP to a non-TATA box cis-regulatory element: a TBP-containing complex activates transcription from snRNA promoters through the PSE. Genes Dev 1993; 7:1535 - 1548
   PubMed Web of Science ®Google Scholar
• Carbon P, Murgo S, Ebel JP, Krol A, Tebb G, Mattaj LW. A common octamer motif binding protein is involved in the transcription of U6 snRNA by RNA polymerase III and U2 snRNA by RNA polymerase II. Cell 1987; 51:71 - 79
   PubMed Web of Science ®Google Scholar
• Bark C, Weller P, Zabielski J, Janson L, Pettersson U. A distant enhancer element is required for polymerase III transcription of a U6 RNA gene. Nature 1987; 328:356 - 359
   PubMed Web of Science ®Google Scholar
• Murphy S, Pierani A, Scheidereit C, Melli M, Roeder RG. Purified octamer binding transcription factors stimulate RNA polymerase III—mediated transcription of the 7SK RNA gene. Cell 1989; 59:1071 - 1080
   PubMed Web of Science ®Google Scholar
• Tanaka M, Lai JS, Herr W. Promoter-selective activation domains in Oct-1 and Oct-2 direct differential activation of an snRNA and mRNA promoter. Cell 1992; 68:755 - 767
   PubMed Web of Science ®Google Scholar
• Schaub M, Myslinski E, Schuster C, Krol A, Carbon P. Staf, a promiscuous activator for enhanced transcription by RNA polymerases II and III. EMBO J 1997; 16:173 - 181
   PubMed Web of Science ®Google Scholar
• Stünkel W, Kober I, Seifart KH. A nucleosome positioned in the distal promoter region activates transcription of the human U6 gene. Mol Cell Biol 1997; 17:4397 - 4405
   PubMed Web of Science ®Google Scholar
• Zhao X, Pendergrast PS, Hernandez N. A positioned nucleosome on the human U6 promoter allows recruitment of SNAPc by the Oct-1 POU domain. Mol Cell 2001; 7:539 - 549
   PubMed Web of Science ®Google Scholar
• Kassavetis GA, Braun BR, Nguyen LH, Geiduschek EP. S. cerevisiae TFIIIB is the transcription initiation factor proper of RNA polymerase III, while TFIIIA and TFIIIC are assembly factors. Cell 1990; 60:235 - 245
   PubMed Web of Science ®Google Scholar
• Teichmann M, Seifart KH. Physical separation of two different forms of human TFIIIB active in the transcription of the U6 or the VAI gene in vitro. EMBO J 1995; 14:5974 - 5983
   PubMed Web of Science ®Google Scholar
• Schramm L, Pendergrast PS, Sun Y, Hernandez N. Different human TFIIIB activities direct RNA polymerase III transcription from TATA-containing and TATA-less promoters. Genes Dev 2000; 14:2650 - 2663
   PubMed Web of Science ®Google Scholar
• Teichmann M, Wang Z, Roeder RG. A stable complex of a novel transcription factor IIB- related factor, human TFIIIB50 and associated proteins mediate selective transcription by RNA polymerase III of genes with upstream promoter elements. Proc Natl Acad Sci USA 2000; 97:14200 - 14205
   PubMed Web of Science ®Google Scholar
• Teichmann M, Dieci G, Huet J, Rüth J, Sentenac A, Seifart KH. Functional interchangeability of TFIIIB components from yeast and human cells in vitro. EMBO J 1997; 16:4708 - 4716
   PubMed Web of Science ®Google Scholar
• Wang Z, Luo T, Roeder RG. Identification of an autonomously initiating RNA polymerase III holoenzyme containing a novel factor that is selectively inactivated during protein synthesis inhibition. Genes Dev 1997; 11:2371 - 2382
   PubMed Web of Science ®Google Scholar
• Dieci G, Sentenac A. Facilitated recycling pathway for RNA polymerase III. Cell 1996; 84:245 - 252
   PubMed Web of Science ®Google Scholar
• Cabart P, Lee J, Willis IM. Facilitated recycling protects human RNA polymerase III from repression by Maf1 in vitro. J Biol Chem 2008; 283:36108 - 36117
   PubMed Web of Science ®Google Scholar
• Wang Z, Roeder RG. DNA topoisomerase I and PC4 can interact with human TFIIIC to promote both accurate termination and transcription reinitiation by RNA polymerase III. Mol Cell 1998; 1:749 - 757
   PubMed Web of Science ®Google Scholar
• Wang Z, Bai L, Hsieh YJ, Roeder RG. Nuclear factor 1 (NF1) affects accurate termination and multiple-round transcription by human RNA polymerase III. EMBO J 2000; 19:6823 - 6832
   PubMed Web of Science ®Google Scholar
• Tavenet A, Suleau A, Dubreuil G, Ferrari R, Ducrot C, Michaut M, et al. Genome-wide location analysis reveals a role for Sub1 in RNA polymerase III transcription. Proc Natl Acad Sci USA 2009; 106:14265 - 14270
   PubMed Web of Science ®Google Scholar
• Rosonina E, Willis IM, Manley JL. Sub1 functions in osmoregulation and in transcription by both RNA polymerases II and III. Mol Cell Biol 2009; 29:2308 - 2321
   PubMed Web of Science ®Google Scholar
• Maraia RJ. Transcription termination factor La is also an initiation factor for RNA polymerase III. Proc Natl Acad Sci USA 1996; 93:3383 - 3387
   PubMed Web of Science ®Google Scholar
• Weser S, Bachmann M, Seifart KH, Meissner W. Transcription efficiency of human polymerase III genes in vitro does not depend on the RNP-forming autoantigen La. Nucleic Acids Res 2000; 28:3935 - 3942
   PubMed Web of Science ®Google Scholar
• French SL, Osheim YN, Schneider DA, Sikes ML, Fernandez CF, Copela LA, et al. Visual analysis of the yeast 5S rRNA gene transcriptome: regulation and role of La protein. Mol Cell Biol 2008; 28:4576 - 4587
   PubMed Web of Science ®Google Scholar
• Fairley JA, Kantidakis T, Kenneth NS, Intine RV, Maraia RJ, White RJ. Human La is found at RNA polymerase III-transcribed genes in vivo. Proc Natl Acad Sci USA 2005; 102:18350 - 18355
   PubMed Web of Science ®Google Scholar
• Kruppa M, Moir RD, Kolodrubetz D, Willis IM. Nhp6, an HMG1 protein, functions in SNR6 transcription by RNA polymerase III in S. cerevisiae. Mol Cell 2001; 7:309 - 318
   PubMed Web of Science ®Google Scholar
• Stillman DJ. Nhp6: a small but powerful effector of chromatin structure in Saccharomyces cerevisiae. Biochim Biophys Acta 2010; 1799:175 - 180
   PubMed Web of Science ®Google Scholar
• Chédin S, Ferri ML, Peyroche G, Andrau JC, Jourdain S, Lefebvre O, et al. The yeast RNA polymerase III transcription machinery: a paradigm for eukaryotic gene activation. Cold Spring Harb Symp Quant Biol 1998; 63:381 - 389
   PubMedGoogle Scholar
• Hu P, Wu S, Sun Y, Yuan CC, Kobayashi R, Myers MP, et al. Characterization of human RNA polymerase III identifies orthologues for Saccharomyces cerevisiae RNA polymerase III subunits. Mol Cell Biol 2002; 22:8044 - 8055
   PubMed Web of Science ®Google Scholar
• Kassavetis GA, Prakash P, Shim E. The C53/C37 subcomplex of RNA polymerase III lies near the active site and participates in promoter opening. J Biol Chem 2010; 285:2695 - 2706
   PubMed Web of Science ®Google Scholar
• Carter R, Drouin G. The increase in the number of subunits in eukaryotic RNA polymerase III relative to RNA polymerase II is due to the permanent recruitment of general transcription factors. Mol Biol Evol 2010; 27:1035 - 1043
   PubMed Web of Science ®Google Scholar
• Valenzuela P, Hager GL, Weinberg F, Rutter WJ. Molecular structure of yeast RNA polymerase III: demonstration of the tripartite transcriptive system in lower eukaryotes. Proc Natl Acad Sci USA 1976; 73:1024 - 1028
   PubMed Web of Science ®Google Scholar
• Werner M, Hermann-Le Denmat S, Treich I, Sentenac A, Thuriaux P. Effect of mutations in a zinc-binding domain of yeast RNA polymerase C (III) on enzyme function and subunit association. Mol Cell Biol 1992; 12:1087 - 1095
   PubMed Web of Science ®Google Scholar
• Thuillier V, Stettler S, Sentenac A, Thuriaux P, Werner M. A mutation in the C31 subunit of Saccharomyces cerevisiae RNA polymerase III affects transcription initiation. EMBO J 1995; 14:351 - 359
   PubMed Web of Science ®Google Scholar
• Werner M, Chaussivert N, Willis IM, Sentenac A. Interaction between a complex of RNA polymerase III subunits and the 70 kDa component of transcription factor IIIB. J Biol Chem 1993; 268:20721 - 20724
   PubMed Web of Science ®Google Scholar
• Brun I, Sentenac A, Werner M. Dual role of the C34 subunit of RNA polymerase III in transcription initiation. EMBO J 1997; 16:5730 - 5741
   PubMed Web of Science ®Google Scholar
• Bartholomew B, Braun BR, Kassavetis GA, Geiduschek EP. Probing close DNA contacts of RNA polymerase III transcription complexes with the photoactive nucleoside 4-thiodeoxythymidine. J Biol Chem 1994; 269:18090 - 18095
   PubMed Web of Science ®Google Scholar
• Wang Z, Roeder RG. Three human RNA polymerase III-specific subunits form a subcomplex with a selective function in specific transcription initiation. Genes Dev 1997; 11:1315 - 1326
   PubMed Web of Science ®Google Scholar
• Hsieh YJ, Kundu TK, Wang Z, Kovelman R, Roeder RG. The TFIIIC90 subunit of TFIIIC interacts with multiple components of the RNA polymerase III machinery and contains a histone-specific acetyltransferase activity. Mol Cell Biol 1999; 19:7697 - 7704
   PubMed Web of Science ®Google Scholar
• Hsieh YJ, Wang Z, Kovelman R, Roeder RG. Cloning and characterization of two evolutionarily conserved subunits (TFIIIC102 and TFIIIC63) of human TFIIIC and their involvement in functional interactions with TFIIIB and RNA polymerase III. Mol Cell Biol 1999; 19:4944 - 4952
   PubMed Web of Science ®Google Scholar
• Schwartz LB, Sklar VE, Jaehning JA, Weinmann R, Roeder RG. Isolation and partial characterization of the multiple forms of deoxyribonucleic acid-dependent ribonucleic acid polymerase in the mouse myeloma, MOPC 315. J Biol Chem 1974; 249:5889 - 5897
   PubMed Web of Science ®Google Scholar
• Sklar VE, Roeder RG. Purification and subunit structure of deoxyribonucleic acid-dependent ribonucleic acid polymerase III from the mouse plasmacytoma, MOPC 315. J Biol Chem 1976; 251:1064 - 1073
   PubMed Web of Science ®Google Scholar
• Paule MR, White RJ. Survey and summary: transcription by RNA polymerases I and III. Nucleic Acids Res 2000; 28:1283 - 1298
   PubMed Web of Science ®Google Scholar
• Li Y, Moir RD, Sethy-Coraci IK, Warner JR, Willis IM. Repression of ribosome and tRNA synthesis in secretion-defective cells is signaled by a novel branch of the cell integrity pathway. Mol Cell Biol 2000; 20:3843 - 3851
   PubMed Web of Science ®Google Scholar
• Willis IM, Desai N, Upadhya R. Signaling repression of transcription by RNA polymerase III in yeast. Prog Nucleic Acid Res Mol Biol 2004; 77:323 - 353
   PubMed Web of Science ®Google Scholar
• Zaragoza D, Ghavidel A, Heitman J, Schultz MC. Rapamycin induces the G0 program of transcriptional repression in yeast by interfering with the TOR signaling pathway. Mol Cell Biol 1998; 18:4463 - 4470
   PubMed Web of Science ®Google Scholar
• Wei Y, Zheng XF. Sch9 partially mediates TORC1 signaling to control ribosomal RNA synthesis. Cell Cycle 2009; 8:4085 - 4090
   PubMed Web of Science ®Google Scholar
• Tsang CK, Liu H, Zheng XF. mTOR binds to the promoters of RNA polymerase I- and III-transcribed genes. Cell Cycle 2010; 9:953 - 957
   PubMed Web of Science ®Google Scholar
• Upadhya R, Lee J, Willis IM. Maf1 is an essential mediator of diverse signals that repress RNA polymerase III transcription. Mol Cell 2002; 10:1489 - 1494
   PubMed Web of Science ®Google Scholar
• Moir RD, Lee J, Haeusler RA, Desai N, Engelke DR, Willis IM. Protein kinase A regulates RNA polymerase III transcription through the nuclear localization of Maf1. Proc Natl Acad Sci USA 2006; 103:15044 - 15049
   PubMed Web of Science ®Google Scholar
• Ciesla M, Boguta M. Regulation of RNA polymerase III transcription by Maf1 protein. Acta Biochim Pol 2008; 55:215 - 225
   PubMed Web of Science ®Google Scholar
• Murawski M, Szczesniak B, Zoładek T, Hopper AK, Martin NC, Boguta M. maf1 mutation alters the subcellular localization of the Mod5 protein in yeast. Acta Biochim Pol 1994; 41:441 - 448
   PubMedGoogle Scholar
• Boguta M, Czerska K, Zoładek T. Mutation in a new gene MAF1 affects tRNA suppressor efficiency in Saccharomyces cerevisiae. Gene 1997; 185:291 - 296
   PubMed Web of Science ®Google Scholar
• Pluta K, Lefebvre O, Martin NC, Smagowicz WJ, Stanford DR, Ellis SR, et al. Maf1p, a negative effector of RNA polymerase III in Saccharomyces cerevisiae. Mol Cell Biol 2001; 21:5031 - 5040
   PubMed Web of Science ®Google Scholar
• Oficjalska-Pham D, Harismendy O, Smagowicz WJ, Gonzalez de Peredo A, Boguta M, Sentenac A, Lefebvre O. General repression of RNA polymerase III transcription is triggered by protein phosphatase type 2A-mediated dephosphorylation of Maf1. Mol Cell 2006; 22:623 - 632
   PubMed Web of Science ®Google Scholar
• Roberts DN, Wilson B, Huff JT, Stewart AJ, Cairns BR. Dephosphorylation and genome-wide association of Maf1 with Pol III-transcribed genes during repression. Mol Cell 2006; 22:633 - 644
   PubMed Web of Science ®Google Scholar
• Willis IM, Moir RD. Integration of nutritional and stress signaling pathways by Maf1. Trends Biochem Sci 2007; 32:51 - 53
   PubMed Web of Science ®Google Scholar
• Lee J, Moir RD, Willis IM. Regulation of RNA polymerase III transcription involves SCH9-dependent and SCH9-independent branches of the target of rapamycin (TOR) pathway. J Biol Chem 2009; 284:12604 - 12608
   PubMed Web of Science ®Google Scholar
• Wei Y, Tsang CK, Zheng XF. Mechanisms of regulation of RNA polymerase III-dependent transcription by TORC1. EMBO J 2009; 28:2220 - 2230
   PubMed Web of Science ®Google Scholar
• Reina JH, Azzouz TN, Hernandez N. Maf1, a new player in the regulation of human NA polymerase III transcription. PLoS ONE 2006; 1:134
   PubMed Web of Science ®Google Scholar
• Rollins J, Veras I, Cabarcas S, Willis I, Schramm L. Human Maf1 negatively regulates NA polymerase III transcription via the TFIIB family members Brf1 and Brf2. Int J Biol Sci 2007; 3:292 - 302
   PubMed Web of Science ®Google Scholar
• Goodfellow SJ, Graham EL, Kantidakis T, Marshall L, Coppins BA, Oficjalska-Pham D, et al. Regulation of RNA polymerase III transcription by Maf1 in mammalian cells. J Mol Biol 2008; 378:481 - 491
   PubMed Web of Science ®Google Scholar
• Johnson SS, Zhang C, Fromm J, Willis IM, Johnson DL. Mammalian Maf1 is a negative regulator of transcription by all three nuclear RNA polymerases. Mol Cell 2007; 26:367 - 379
   PubMed Web of Science ®Google Scholar
• Ginsberg AM, King BO, Roeder RG. Xenopus 5S gene transcription factor, TFIIIA: characterization of a cDNA clone and measurement of RNA levels throughout development. Cell 1984; 39:479 - 489
   PubMed Web of Science ®Google Scholar
• Miller J, McLachlan AD, Klug A. Repetitive zinc-binding domains in the protein transcription factor IIIA from Xenopus oocytes. EMBO J 1985; 4:1609 - 1614
   PubMed Web of Science ®Google Scholar
• Honda BM, Roeder RG. Association of a 5S gene transcription factor with 5S RNA and altered levels of the factor during cell differentiation. Cell 1980; 22:119 - 126
   PubMed Web of Science ®Google Scholar
• Shastry BS, Honda BM, Roeder RG. Altered levels of a 5 S gene-specific transcription factor (TFIIIA) during oogenesis and embryonic development of Xenopus laevis. J Biol Chem 1984; 259:11373 - 11382
   PubMed Web of Science ®Google Scholar
• Wolffe AP, Brown DD. Developmental regulation of two 5S ribosomal RNA genes. Science 1988; 241:1626 - 1632
   PubMed Web of Science ®Google Scholar
• Wolffe AP. Dominant and specific repression of Xenopus oocyte 5S RNA genes and satellite I DNA by histone H1. EMBO J 1989; 8:527 - 537
   PubMed Web of Science ®Google Scholar
• Taylor W, Jackson IJ, Siegel N, Kumar A, Brown DD. The developmental expression of the gene for TFIIIA in Xenopus laevis. Nucleic Acids Res 1986; 14:6185 - 6195
   PubMed Web of Science ®Google Scholar
• Martinez E, Lagna G, Roeder RG. Overlapping transcription by RNA polymerases II and III of the Xenopus TFIIIA gene in somatic cells. J Biol Chem 1994; 269:25692 - 25698
   PubMed Web of Science ®Google Scholar
• Segall J, Matsui T, Roeder RG. Multiple factors are required for the accurate transcription of purified genes by RNA polymerase III. J Biol Chem 1980; 255:11986 - 11991
   PubMed Web of Science ®Google Scholar
• Matsui T, Segall J, Weil PA, Roeder RG. Multiple factors required for accurate initiation of transcription by purified RNA polymerase II. J Biol Chem 1980; 255:11992 - 11996
   PubMed Web of Science ®Google Scholar
• Grummt I, Roth E, Paule MR. Ribosomal RNA transcription in vitro is species specific. Nature 1982; 296:173 - 174
   PubMed Web of Science ®Google Scholar
• Roeder RG. Lasker Basic Medical Research Award. The eukaryotic transcriptional machinery: complexities and mechanisms unforeseen. Nat Med 2003; 9:1239 - 1244
   PubMed Web of Science ®Google Scholar
• Juven-Gershon T, Kadonaga JT. Regulation of gene expression via the core promoter and the basal transcriptional machinery. Dev Biol 2010; 339:225 - 229
   PubMed Web of Science ®Google Scholar
• Drygin D, Rice WG, Grummt I. The RNA polymerase I transcription machinery: an emerging target for the treatment of cancer. Annu Rev Pharmacol Toxicol 2010; 50:131 - 156
   PubMed Web of Science ®Google Scholar
• Berger SL, Folk WR. Differential activation of RNA polymerase III-transcribed genes by the polyomavirus enhancer and the adenovirus E1A gene products. Nucleic Acids Res 1985; 13:1413 - 1428
   PubMed Web of Science ®Google Scholar
• Hoeffler WK, Roeder RG. Enhancement of RNA polymerase III transcription by the E1A gene product of adenovirus. Cell 1985; 41:955 - 963
   PubMed Web of Science ®Google Scholar
• Gaynor RB, Feldman LT, Berk AJ. Transcription of class III genes activated by viral immediate early proteins. Science 1985; 230:447 - 450
   PubMed Web of Science ®Google Scholar
• Yoshinaga S, Dean N, Han M, Berk AJ. Adenovirus stimulation of transcription by RNA polymerase III: evidence for an E1A-dependent increase in transcription factor IIIC concentration. EMBO J 1986; 5:343 - 354
   PubMed Web of Science ®Google Scholar
• Sinn E, Wang Z, Kovelman R, Roeder RG. Cloning and characterization of a TFIIIC2 subunit (TFIIICbeta) whose presence correlates with activation of RNA polymerase III-mediated transcription by adenovirus E1A expression and serum factors. Genes Dev 1995; 9:675 - 685
   PubMed Web of Science ®Google Scholar
• Patel G, Jones NC. Activation in vitro of RNA polymerase II and III directed transcription by baculovirus produced E1A protein. Nucleic Acids Res 1990; 18:2909 - 2915
   PubMed Web of Science ®Google Scholar
• Loeken M, Bikel I, Livingston DM, Brady J. Transactivation of RNA polymerase II and III promoters by SV40 small t antigen. Cell 1988; 55:1171 - 1177
   PubMed Web of Science ®Google Scholar
• Aufiero B, Schneider RJ. The hepatitis B virus X-gene product trans-activates both RNA polymerase II and III promoters. EMBO J 1990; 9:497 - 504
   PubMed Web of Science ®Google Scholar
• Wang HD, Yuh CH, Dang CV, Johnson DL. The hepatitis B virus X protein increases the cellular level of TATA-binding protein, which mediates transactivation of RNA polymerase III genes. Mol Cell Biol 1995; 15:6720 - 6728
   PubMed Web of Science ®Google Scholar
• Levine AJ. The common mechanisms of transformation by the small DNA tumor viruses: The inactivation of tumor suppressor gene products: p53. Virology 2009; 384:285 - 293
   PubMed Web of Science ®Google Scholar
• DeCaprio JA. How the Rb tumor suppressor structure and function was revealed by the study of Adenovirus and SV40. Virology 2009; 384:274 - 284
   PubMed Web of Science ®Google Scholar
• White RJ, Trouche D, Martin K, Jackson SP, Kouzarides T. Repression of RNA polymerase III transcription by the retinoblastoma protein. Nature 1996; 382:88 - 90
   PubMed Web of Science ®Google Scholar
• Chu WM, Wang Z, Roeder RG, Schmid CW. RNA polymerase III transcription repressed by Rb through its interactions with TFIIIB and TFIIIC2. J Biol Chem 1997; 272:14755 - 14761
   PubMed Web of Science ®Google Scholar
• Chesnokov I, Chu WM, Botchan MR, Schmid CW. p53 inhibits RNA polymerase III-directed transcription in a promoter-dependent manner. Mol Cell Biol 1996; 16:7084 - 7088
   PubMed Web of Science ®Google Scholar
• Cairns CA, White RJ. p53 is a general repressor of RNA polymerase III transcription. EMBO J 1998; 17:3112 - 3123
   PubMed Web of Science ®Google Scholar
• Morton JP, Kantidakis T, White RJ. RNA polymerase III transcription is repressed in response to the tumour suppressor ARF. Nucleic Acids Res 2007; 35:3046 - 3052
   PubMed Web of Science ®Google Scholar
• Woiwode A, Johnson SA, Zhong S, Zhang C, Roeder RG, Teichmann M, et al. PTEN represses RNA polymerase III-dependent transcription by targeting the TFIIIB complex. Mol Cell Biol 2008; 28:4204 - 4214
   PubMed Web of Science ®Google Scholar
• Veras I, Rosen EM, Schramm L. Inhibition of RNA polymerase III transcription by BRCA1. J Mol Biol 2009; 387:523 - 531
   PubMed Web of Science ®Google Scholar
• Larminie CG, Cairns CA, Mital R, Martin K, Kouzarides T, Jackson SP, White RJ. Mechanistic analysis of RNA polymerase III regulation by the retinoblastoma protein. EMBO J 1997; 16:2061 - 2071
   PubMed Web of Science ®Google Scholar
• Hirsch HA, Jawdekar GW, Lee KA, Gu L, Henry RW. Distinct mechanisms for repression of RNA polymerase III transcription by the retinoblastoma tumor suppressor protein. Mol Cell Biol 2004; 24:5989 - 5999
   PubMed Web of Science ®Google Scholar
• Eichhorn K, Jackson SP. A role for TAF3B2 in the repression of human RNA polymerase III transcription in nonproliferating cells. J Biol Chem 2001; 276:21158 - 21165
   PubMed Web of Science ®Google Scholar
• Sutcliffe JE, Cairns CA, McLees A, Allison SJ, Tosh K, White RJ. RNA polymerase III transcription factor IIIB is a target for repression by pocket proteins p107 and p130. Mol Cell Biol 1999; 19:4255 - 4261
   PubMed Web of Science ®Google Scholar
• White RJ. RNA polymerases I and III, growth control and cancer. Nat Rev Mol Cell Biol 2005; 6:69 - 78
   PubMed Web of Science ®Google Scholar
• Gottesfeld JM, Wolf VJ, Dang T, Forbes DJ, Hartl P. Mitotic repression of RNA polymerase III transcription in vitro mediated by phosphorylation of a TFIIIB component. Science 1994; 263:81 - 84
   PubMed Web of Science ®Google Scholar
• Leresche A, Wolf VJ, Gottesfeld JM. Repression of RNA polymerase II and III transcription during M phase of the cell cycle. Exp Cell Res 1996; 229:282 - 288
   PubMed Web of Science ®Google Scholar
• White RJ, Gottlieb TM, Downes CS, Jackson SP. Mitotic regulation of a TATA-binding-protein-containing complex. Mol Cell Biol 1995; 15:1983 - 1992
   PubMed Web of Science ®Google Scholar
• Fairley JA, Scott PH, White RJ. TFIIIB is phosphorylated, disrupted and selectively released from tRNA promoters during mitosis in vivo. EMBO J 2003; 22:5841 - 5850
   PubMed Web of Science ®Google Scholar
• Hu P, Samudre K, Wu S, Sun Y, Hernandez N. CK2 phosphorylation of Bdp1 executes cell cycle-specific RNA polymerase III transcription repression. Mol Cell 2004; 16:81 - 92
   PubMed Web of Science ®Google Scholar
• Hu P, Wu S, Hernandez N. A minimal RNA polymerase III transcription system from human cells reveals positive and negative regulatory roles for CK2. Mol Cell 2003; 12:699 - 709
   PubMed Web of Science ®Google Scholar
• Ghavidel A, Hockman DJ, Schultz MC. A review of progress towards elucidating the role of protein kinase CK2 in polymerase III transcription: regulation of the TATA binding protein. Mol Cell Biochem 1999; 191:143 - 148
   PubMed Web of Science ®Google Scholar
• Ghavidel A, Schultz MC. TATA binding protein-associated CK2 transduces DNA damage signals to the RNA polymerase III transcriptional machinery. Cell 2001; 106:575 - 584
   PubMed Web of Science ®Google Scholar
• Dephoure N, Zhou C, Villén J, Beausoleil SA, Bakalarski CE, Elledge SJ, et al. A quantitative atlas of mitotic phosphorylation. Proc Natl Acad Sci USA 2008; 105:10762 - 10767
   PubMed Web of Science ®Google Scholar
• Gu L, Husain-Ponnampalam R, Hoffmann-Benning S, Henry RW. The protein kinase CK2 phosphorylates SNAP190 to negatively regulate SNAPC DNA binding and human U6 transcription by RNA polymerase III. J Biol Chem 2007; 282:27887 - 27896
   PubMed Web of Science ®Google Scholar
• Gomez-Roman N, Grandori C, Eisenman RN, White RJ. Direct activation of RNA polymerase III transcription by c-Myc. Nature 2003; 421:290 - 294
   PubMed Web of Science ®Google Scholar
• Felton-Edkins ZA, Fairley JA, Graham EL, Johnston IM, White RJ, Scott PH. The mitogen-activated protein (MAP) kinase ERK induces tRNA synthesis by phosphorylating TFIIIB. EMBO J 2003; 22:2422 - 2432
   PubMed Web of Science ®Google Scholar
• Zhong S, Johnson DL. The JNKs differentially regulate RNA polymerase III transcription by coordinately modulating the expression of all TFIIIB subunits. Proc Natl Acad Sci USA 2009; 106:12682 - 12687
   PubMed Web of Science ®Google Scholar
• Kenneth NS, Ramsbottom BA, Gomez-Roman N, Marshall L, Cole PA, White RJ. TRRAP and GCN5 are used by c-Myc to activate RNA polymerase III transcription. Proc Natl Acad Sci USA 2007; 104:14917 - 14922
   PubMed Web of Science ®Google Scholar
• Dai MS, Sun XX, Lu H. Ribosomal protein L11 associates with c-Myc at 5 S rRNA and tRNA genes and regulates their expression. J Biol Chem 2010; 285:12587 - 12594
   PubMed Web of Science ®Google Scholar
• Steiger D, Furrer M, Schwinkendorf D, Gallant P. Max-independent functions of Myc in Drosophila melanogaster. Nat Genet 2008; 40:1084 - 1091
   PubMed Web of Science ®Google Scholar
• Greasley PJ, Bonnard C, Amati B. Myc induces the nucleolin and BN51 genes: possible implications in ribosome biogenesis. Nucleic Acids Res 2000; 28:446 - 453
   PubMed Web of Science ®Google Scholar
• Ittmann M, Greco A, Basilico C. Isolation of the human gene that complements a temperature-sensitive cell cycle mutation in BHK cells. Mol Cell Biol 1987; 7:3386 - 3393
   PubMed Web of Science ®Google Scholar
• Ittmann M, Ali J, Greco A, Basilico C. The gene complementing a temperature-sensitive cell cycle mutant of BHK cells is the human homologue of the yeast RPC53 gene, which encodes a subunit of RNA polymerase C (III). Cell Growth Differ 1993; 4:503 - 511
   PubMedGoogle Scholar
• Mann C, Micouin JY, Chiannilkulchai N, Treich I, Buhler JM, Sentenac A. RPC53 encodes a subunit of Saccharomyces cerevisiae RNA polymerase C (III) whose inactivation leads to a predominantly G1 arrest. Mol Cell Biol 1992; 12:4314 - 4326
   PubMed Web of Science ®Google Scholar
• Winter AG, Sourvinos G, Allison SJ, Tosh K, Scott PH, Spandidos DA, White RJ. RNA polymerase III transcription factor TFIIIC2 is overexpressed in ovarian tumors. Proc Natl Acad Sci USA 2000; 97:12619 - 12624
   PubMed Web of Science ®Google Scholar
• Marshall L, Kenneth NS, White RJ. Elevated tRNA(iMet) synthesis can drive cell proliferation and oncogenic transformation. Cell 2008; 133:78 - 89
   PubMed Web of Science ®Google Scholar
• Johnson SA, Dubeau L, Johnson DL. Enhanced RNA polymerase III-dependent transcription is required for oncogenic transformation. J Biol Chem 2008; 283:19184 - 19191
   PubMed Web of Science ®Google Scholar
• Hinault C, Hu J, Maier BF, Mirmira RG, Kulkarni RN. Differential expression of cell cycle proteins during ageing of pancreatic islet cells. Diabetes Obes Metab 2008; 10:136 - 146
   PubMed Web of Science ®Google Scholar
• Bouwens L, Rooman I. Regulation of pancreatic betacell mass. Physiol Rev 2005; 85:1255 - 1270
   PubMed Web of Science ®Google Scholar
• Atanasoski S, Notterpek L, Lee HY, Castagner F, Young P, Ehrengruber MU, et al. The protooncogene Ski controls Schwann cell proliferation and myelination. Neuron 2004; 43:499 - 511
   PubMed Web of Science ®Google Scholar
• Goodfellow SJ, Innes F, Derblay LE, MacLellan WR, Scott PH, White RJ. Regulation of RNA polymerase III transcription during hypertrophic growth. EMBO J 2006; 25:1522 - 1533
   PubMed Web of Science ®Google Scholar
• Blum B, Benvenisty N. The tumorigenicity of diploid and aneuploid human pluripotent stem cells. Cell Cycle 2009; 8:3822 - 3830
   PubMed Web of Science ®Google Scholar
• White RJ, Stott D, Rigby PW. Regulation of RNA polymerase III transcription in response to F9 embryonal carcinoma stem cell differentiation. Cell 1989; 59:1081 - 1092
   PubMed Web of Science ®Google Scholar
• Meissner W, Thomae R, Seifart KH. The activity of transcription factor IIIC1 is impaired during differentiation of F9 cells. J Biol Chem 2002; 277:7148 - 7156
   PubMed Web of Science ®Google Scholar
• Alzuherri HM, White RJ. Regulation of a TATA-binding protein-associated factor during cellular differentiation. J Biol Chem 1998; 273:17166 - 17171
   PubMed Web of Science ®Google Scholar
• Athineos D, Marshall L, White RJ. Regulation of TFIIIB during F9 cell differentiation. BMC Mol Biol 2010; 11:21
   PubMed Web of Science ®Google Scholar
• Meissner W, Ahlers A, Seifart KH. The activity of transcription factor PBP, which binds to the proximal sequence element of mammalian U6 genes, is regulated during differentiation of F9 cells. Mol Cell Biol 1995; 15:5888 - 5897
   PubMed Web of Science ®Google Scholar
• Weser S, Gruber C, Hafner HM, Teichmann M, Roeder RG, Seifart KH, et al. Transcription factor (TF)-like nuclear regulator, the 250 kDa form of Homo sapiens TFIIIB”, is an essential component of human TFIIIC1 activity. J Biol Chem 2004; 279:27022 - 27029
   PubMed Web of Science ®Google Scholar
• Dean N, Berk AJ. Separation of TFIIIC into two functional components by sequence specific DNA affinity chromatography. Nucleic Acids Res 1987; 15:9895 - 9907
   PubMed Web of Science ®Google Scholar
• Yoshinaga SK, Boulanger PA, Berk AJ. Resolution of human transcription factor TFIIIC into two functional components. Proc Natl Acad Sci USA 1987; 84:3585 - 3589
   PubMed Web of Science ®Google Scholar
• Oettel S, Härtel F, Kober I, Iben S, Seifart KH. Human transcription factors IIIC2, IIIC1 and a novel component IIIC0 fulfil different aspects of DNA binding to various pol III genes. Nucleic Acids Res 1997; 25:2440 - 2447
   PubMed Web of Science ®Google Scholar
• Yee NS, Gong W, Huang Y, Lorent K, Dolan AC, Maraia RJ, Pack M. Mutation of RNA Pol III subunit rpc2/polr3b Leads to Deficiency of Subunit Rpc11 and disrupts zebrafish digestive development. PLoS Biol 2007; 5:312
   PubMed Web of Science ®Google Scholar
• Dittmar KA, Goodenbour JM, Pan T. Tissue-specific differences in human transfer RNA expression. PLoS Genet 2006; 2:221
   PubMed Web of Science ®Google Scholar
• Barski A, Chepelev I, Liko D, Cuddapah S, Fleming AB, Birch J, et al. Pol II and its associated epigenetic marks are present at Pol III-transcribed noncoding RNA genes. Nat Struct Mol Biol 2010; 17:629 - 634
   PubMed Web of Science ®Google Scholar
• Canella D, Praz V, Reina JH, Cousin P, Hernandez N. Defining the RNA polymerase III transcriptome: Genome-wide localization of the RNA polymerase III transcription machinery in human cells. Genome Res 2010; 20:710 - 721
   PubMed Web of Science ®Google Scholar
• Moqtaderi Z, Wang J, Raha D, White RJ, Snyder M, Weng Z, Struhl K. Genomic binding profiles of functionally distinct RNA polymerase III transcription complexes in human cells. Nat Struct Mol Biol 2010; 17:635 - 640
   PubMed Web of Science ®Google Scholar
• Oler AJ, Alla RK, Roberts DN, Wong A, Hollenhorst PC, Chandler KJ, et al. Human RNA polymerase III transcriptomes and relationships to Pol II promoter chromatin and enhancer-binding factors. Nat Struct Mol Biol 2010; 17:620 - 628
   PubMed Web of Science ®Google Scholar
• Raha D, Wang Z, Moqtaderi Z, Wu L, Zhong G, Gerstein M, et al. Close association of RNA polymerase II and many transcription factors with Pol III genes. Proc Natl Acad Sci USA 2010; 107:3639 - 3644
   PubMed Web of Science ®Google Scholar
• Tiedge H, Chen W, Brosius J. Primary structure, neural-specific expression and dendritic location of human BC200 RNA. J Neurosci 1993; 13:2382 - 2390
   PubMed Web of Science ®Google Scholar
• Ozsolak F, Poling LL, Wang Z, Liu H, Liu XS, Roeder RG, et al. Chromatin structure analyses identify miRNA promoters. Genes Dev 2008; 22:3172 - 3183
   PubMed Web of Science ®Google Scholar
• Borchert GM, Lanier W, Davidson BL. RNA polymerase III transcribes human microRNAs. Nat Struct Mol Biol 2006; 13:1097 - 1101
   PubMed Web of Science ®Google Scholar
• Noma K, Cam HP, Maraia RJ, Grewal SI. A role for TFIIIC transcription factor complex in genome organization. Cell 2006; 125:859 - 872
   PubMed Web of Science ®Google Scholar
• Mertens C, Roeder RG. Different functional modes of p300 in activation of RNA polymerase III transcription from chromatin templates. Mol Cell Biol 2008; 28:5764 - 5776
   PubMed Web of Science ®Google Scholar
• Dubey RN, Gartenberg MR. A tDNA establishes cohesion of a neighboring silent chromatin domain. Genes Dev 2007; 21:2150 - 2160
   PubMed Web of Science ®Google Scholar
• Kalkhoven E. CBP and p300: HATs for different occasions. Biochem Pharmacol 2004; 68:1145 - 1155
   PubMed Web of Science ®Google Scholar
• Haeusler RA, Engelke DR. Genome organization in three dimensions: thinking outside the line. Cell Cycle 2004; 3:273 - 275
   PubMed Web of Science ®Google Scholar
• Haeusler RA, Pratt-Hyatt M, Good PD, Gipson TA, Engelke DR. Clustering of yeast tRNA genes is mediated by specific association of condensin with tRNA gene transcription complexes. Genes Dev 2008; 22:2204 - 2214
   PubMed Web of Science ®Google Scholar
• Pollock C, Huang S. The perinucleolar compartment. Cold Spring Harb Perspect Biol 2010; 2:000679
   Web of Science ®Google Scholar