Literature DB >> 9606193

p53 is a general repressor of RNA polymerase III transcription.

C A Cairns1, R J White.   

Abstract

p53 is a major tumour suppressor that is inactivated in a large proportion of human cancers. We show that p53 serves as a general repressor of transcription by RNA polymerase (pol) III. It can inhibit the synthesis of a range of essential small cellular RNAs including tRNA, 5S rRNA and U6 snRNA, as well as viral products such as the adenovirus VAI RNA. Fibroblasts derived from p53 knock-out mice display a substantial increase in pol III transcriptional activity. Endogenous cellular p53 is shown to interact with the TATA-binding protein (TBP)-containing general factor TFIIIB, thereby compromising its function severely. However, assembly of TFIIIB into a pre-initiation complex confers substantial protection against the inhibitory effects of p53. Since TFIIIB is an essential determinant of the biosynthetic capacity of cells, its release from repression by p53 may contribute to a loss of growth control during the development of many tumours.

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Year:  1998        PMID: 9606193      PMCID: PMC1170650          DOI: 10.1093/emboj/17.11.3112

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  62 in total

Review 1.  Transcription by RNA polymerases I and III: a potential link between cell growth, protein synthesis and the retinoblastoma protein.

Authors:  C G Larminie; H M Alzuherri; C A Cairns; A McLees; R J White
Journal:  J Mol Med (Berl)       Date:  1998-02       Impact factor: 4.599

2.  Regulation of pre-transfer RNA synthesis during transition from resting to growing state.

Authors:  J C Mauck; H Green
Journal:  Cell       Date:  1974-10       Impact factor: 41.582

3.  Two domains of p53 interact with the TATA-binding protein, and the adenovirus 13S E1A protein disrupts the association, relieving p53-mediated transcriptional repression.

Authors:  N Horikoshi; A Usheva; J Chen; A J Levine; R Weinmann; T Shenk
Journal:  Mol Cell Biol       Date:  1995-01       Impact factor: 4.272

4.  Mitotic regulation of a TATA-binding-protein-containing complex.

Authors:  R J White; T M Gottlieb; C S Downes; S P Jackson
Journal:  Mol Cell Biol       Date:  1995-04       Impact factor: 4.272

5.  Transcriptional regulation of the PCNA promoter by p53.

Authors:  P Jackson; P Ridgway; J Rayner; J Noble; A Braithwaite
Journal:  Biochem Biophys Res Commun       Date:  1994-08-30       Impact factor: 3.575

6.  p53 transcriptional activation mediated by coactivators TAFII40 and TAFII60.

Authors:  C J Thut; J L Chen; R Klemm; R Tjian
Journal:  Science       Date:  1995-01-06       Impact factor: 47.728

7.  Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei.

Authors:  J D Dignam; R M Lebovitz; R G Roeder
Journal:  Nucleic Acids Res       Date:  1983-03-11       Impact factor: 16.971

8.  Differential regulation of RNA polymerases I, II, and III by the TBP-binding repressor Dr1.

Authors:  R J White; B C Khoo; J A Inostroza; D Reinberg; S P Jackson
Journal:  Science       Date:  1994-10-21       Impact factor: 47.728

9.  p53-dependent repression of CDK4 translation in TGF-beta-induced G1 cell-cycle arrest.

Authors:  M E Ewen; C J Oliver; H K Sluss; S J Miller; D S Peeper
Journal:  Genes Dev       Date:  1995-01-15       Impact factor: 11.361

10.  Transcriptional activation by p53 correlates with suppression of growth but not transformation.

Authors:  T Crook; N J Marston; E A Sara; K H Vousden
Journal:  Cell       Date:  1994-12-02       Impact factor: 41.582

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  76 in total

1.  5S ribosomal RNA database Y2K.

Authors:  M Szymanski; M Z Barciszewska; J Barciszewski; V A Erdmann
Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

Review 2.  Survey and summary: transcription by RNA polymerases I and III.

Authors:  M R Paule; R J White
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

3.  RNA polymerase III transcription factor IIIB is a target for repression by pocket proteins p107 and p130.

Authors:  J E Sutcliffe; C A Cairns; A McLees; S J Allison; K Tosh; R J White
Journal:  Mol Cell Biol       Date:  1999-06       Impact factor: 4.272

Review 4.  RNA polymerase III transcription: its control by tumor suppressors and its deregulation by transforming agents.

Authors:  T R Brown; P H Scott; T Stein; A G Winter; R J White
Journal:  Gene Expr       Date:  2000

5.  Retinoblastoma protein disrupts interactions required for RNA polymerase III transcription.

Authors:  J E Sutcliffe; T R Brown; S J Allison; P H Scott; R J White
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

6.  The mitogen-activated protein (MAP) kinase ERK induces tRNA synthesis by phosphorylating TFIIIB.

Authors:  Zoe A Felton-Edkins; Jennifer A Fairley; Emma L Graham; Imogen M Johnston; Robert J White; Pamela H Scott
Journal:  EMBO J       Date:  2003-05-15       Impact factor: 11.598

7.  The tumor suppressor p53 inhibits Net, an effector of Ras/extracellular signal-regulated kinase signaling.

Authors:  Koji Nakade; Hong Zheng; Gitali Ganguli; Gilles Buchwalter; Christian Gross; Bohdan Wasylyk
Journal:  Mol Cell Biol       Date:  2004-02       Impact factor: 4.272

Review 8.  p53, a translational regulator: contribution to its tumour-suppressor activity.

Authors:  V Marcel; F Catez; J-J Diaz
Journal:  Oncogene       Date:  2015-03-02       Impact factor: 9.867

9.  Maf1p, a negative effector of RNA polymerase III in Saccharomyces cerevisiae.

Authors:  K Pluta; O Lefebvre; N C Martin; W J Smagowicz; D R Stanford; S R Ellis; A K Hopper; A Sentenac; M Boguta
Journal:  Mol Cell Biol       Date:  2001-08       Impact factor: 4.272

10.  TFIIIB is phosphorylated, disrupted and selectively released from tRNA promoters during mitosis in vivo.

Authors:  Jennifer A Fairley; Pamela H Scott; Robert J White
Journal:  EMBO J       Date:  2003-11-03       Impact factor: 11.598

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