Literature DB >> 8943346

TATA-binding protein is limiting for both TATA-containing and TATA-lacking RNA polymerase III promoters in Drosophila cells.

A Trivedi1, A Vilalta, S Gopalan, D L Johnson.   

Abstract

We have investigated the role of the TATA-binding protein (TBP) in modulating RNA polymerase (Pol) III gene activity. Epitope-tagged TBP (e-TBP) was both transiently and stably transfected in Drosophila Schneider S-2 cells to increase the total cellular level of TBP. Analysis of the transcripts synthesized from cotransfected tRNA and U6 RNA genes revealed that both types of RNA Pol III promoters were substantially stimulated by an increase in e-TBP in a dose-dependent manner. Furthermore, a TBP-dependent increase in the levels of endogenous tRNA transcripts was produced in the stable line induced to express the e-TBP. We further determined whether the ability of increased TBP to induce RNA Pol III gene expression was due to a direct effect of increased TBP complexes on RNA Pol III gene promoters or an indirect consequence of enhanced expression of RNA Pol II genes. A TBP expression plasmid (e-TBP332), containing a mutation within the highly conserved carboxy-terminal domain, was both transiently and stably transfected into S-2 cells. e-TBP332 augmented the transcription from two RNA Pol II gene promoters indistinguishably from that observed when e-TBP was expressed. In contrast, e-TBP332 was completely defective in its ability to stimulate either the tRNA or U6 RNA gene promoters. In addition, increasing levels of a truncated TBP protein containing only the carboxy-terminal region failed to induce either the tRNA or U6 RNA gene promoter, whereas it retained its ability to stimulate an RNA Pol II promoter. Thus, the TBP-dependent increase in RNA Pol II gene activity is not sufficient for enhanced RNA Pol III gene transcription; rather, a direct effect on RNA Pol III promoters is required. Furthermore, these results provide the first direct evidence that the amino-terminal region of TBP is important for the formation or function of TBP-containing complexes utilized by TATA-less and TATA-containing RNA Pol III promoters. Together, these studies demonstrate that TBP is limiting for the expression of both classes of RNA Pol III promoters in Drosophila cells and implicate an important role for TBP in regulating RNA Pol III gene expression.

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Year:  1996        PMID: 8943346      PMCID: PMC231694          DOI: 10.1128/MCB.16.12.6909

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  44 in total

1.  A TBP complex essential for transcription from TATA-less but not TATA-containing RNA polymerase III promoters is part of the TFIIIB fraction.

Authors:  S M Lobo; M Tanaka; M L Sullivan; N Hernandez
Journal:  Cell       Date:  1992-12-11       Impact factor: 41.582

2.  The rat vault RNA gene contains a unique RNA polymerase III promoter composed of both external and internal elements that function synergistically.

Authors:  A Vilalta; V A Kickhoefer; L H Rome; D L Johnson
Journal:  J Biol Chem       Date:  1994-11-25       Impact factor: 5.157

3.  Mitotic repression of RNA polymerase III transcription in vitro mediated by phosphorylation of a TFIIIB component.

Authors:  J M Gottesfeld; V J Wolf; T Dang; D J Forbes; P Hartl
Journal:  Science       Date:  1994-01-07       Impact factor: 47.728

4.  Regional codon randomization: defining a TATA-binding protein surface required for RNA polymerase III transcription.

Authors:  B P Cormack; K Struhl
Journal:  Science       Date:  1993-10-08       Impact factor: 47.728

5.  Crystal structure of yeast TATA-binding protein and model for interaction with DNA.

Authors:  D I Chasman; K M Flaherty; P A Sharp; R D Kornberg
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-01       Impact factor: 11.205

6.  Conserved and nonconserved functions of the yeast and human TATA-binding proteins.

Authors:  B P Cormack; M Strubin; L A Stargell; K Struhl
Journal:  Genes Dev       Date:  1994-06-01       Impact factor: 11.361

7.  The TATA-binding protein and associated factors are components of pol III transcription factor TFIIIB.

Authors:  A K Taggart; T S Fisher; B F Pugh
Journal:  Cell       Date:  1992-12-11       Impact factor: 41.582

8.  A suppressor of TBP mutations encodes an RNA polymerase III transcription factor with homology to TFIIB.

Authors:  S Buratowski; H Zhou
Journal:  Cell       Date:  1992-10-16       Impact factor: 41.582

9.  Induction of Drosophila RNA polymerase III gene expression by the phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA) is mediated by transcription factor IIIB.

Authors:  M E Garber; A Vilalta; D L Johnson
Journal:  Mol Cell Biol       Date:  1994-01       Impact factor: 4.272

10.  The N-terminal domain of the human TATA-binding protein plays a role in transcription from TATA-containing RNA polymerase II and III promoters.

Authors:  A Lescure; Y Lutz; D Eberhard; X Jacq; A Krol; I Grummt; I Davidson; P Chambon; L Tora
Journal:  EMBO J       Date:  1994-03-01       Impact factor: 11.598

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  18 in total

Review 1.  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

2.  A differential response of wild type and mutant promoters to TFIIIB70 overexpression in vivo and in vitro.

Authors:  I Sethy-Coraci; R D Moir; A López-de-León; I M Willis
Journal:  Nucleic Acids Res       Date:  1998-05-15       Impact factor: 16.971

3.  The Drosophila TATA binding protein contains a strong but masked activation domain.

Authors:  M Um; J L Manley
Journal:  Gene Expr       Date:  2000

4.  Abnormal expression of TFIIIB subunits and RNA Pol III genes is associated with hepatocellular carcinoma.

Authors:  Junxia Lei; Songlin Chen; Shuping Zhong
Journal:  Liver Res       Date:  2017-09-09

5.  A review of progress towards elucidating the role of protein kinase CK2 in polymerase III transcription: regulation of the TATA binding protein.

Authors:  A Ghavidel; D J Hockman; M C Schultz
Journal:  Mol Cell Biochem       Date:  1999-01       Impact factor: 3.396

6.  Hepatitis B virus X protein induces RNA polymerase III-dependent gene transcription and increases cellular TATA-binding protein by activating the Ras signaling pathway.

Authors:  H D Wang; A Trivedi; D L Johnson
Journal:  Mol Cell Biol       Date:  1997-12       Impact factor: 4.272

7.  Heterozygous disruption of the TATA-binding protein gene in DT40 cells causes reduced cdc25B phosphatase expression and delayed mitosis.

Authors:  M Um; J Yamauchi; S Kato; J L Manley
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

8.  Biochemical and genetic characterization of the dominant positive element driving transcription ofthe yeast TBP-encoding gene, SPT15.

Authors:  S C Schroeder; P A Weil
Journal:  Nucleic Acids Res       Date:  1998-09-15       Impact factor: 16.971

9.  TBP is differentially regulated by c-Jun N-terminal kinase 1 (JNK1) and JNK2 through Elk-1, controlling c-Jun expression and cell proliferation.

Authors:  Shuping Zhong; Jody Fromm; Deborah L Johnson
Journal:  Mol Cell Biol       Date:  2006-10-30       Impact factor: 4.272

Review 10.  Dysregulation of the basal RNA polymerase transcription apparatus in cancer.

Authors:  Megan J Bywater; Richard B Pearson; Grant A McArthur; Ross D Hannan
Journal:  Nat Rev Cancer       Date:  2013-05       Impact factor: 60.716

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