Literature DB >> 8264601

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

M E Garber1, A Vilalta, D L Johnson.   

Abstract

We have previously found that the phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA) induces specific transcription of tRNA and 5S RNA genes in Drosophila Schneider S-2 cells (M. Garber, S. Panchanathan, R. F. Fan, and D. L. Johnson, J. Biol. Chem. 266:20598-20601, 1991). Having derived cellular extracts from TPA-treated cells, that are capable of reproducing this stimulation in vitro, we have examined the mechanism for this regulatory event. Using conditions that limit reinitiation and produce single rounds of transcription from active gene complexes, we find that the number of functional transcription complexes is increased in extracts prepared from TPA-induced cells. We have analyzed the activities of the transcription factors TFIIIB and TFIIIC derived from extracts prepared from TPA-induced and noninduced cells. Examination of the relative activities of TFIIIC showed that both its ability to reconstitute transcription with TFIIIB and RNA polymerase III and its ability to stably bind to the DNA template are unchanged. However, the activity of TFIIIB derived from the TPA-induced cells is substantially increased compared with that derived from the noninduced cells. The differences in TFIIIB activity account for the differences in the overall transcriptional activities observed in the unfractionated extracts. Western blot analysis of the TATA-binding protein subunit of TFIIIB revealed that there is an increase in the amount of this polypeptide present in the induced cell extracts and TFIIIB fraction. Together, these results indicate that the TPA response in Drosophila cells stimulates specific transcription of RNA polymerase III genes by increasing the activity of the limiting transcription component, TFIIIB, and thereby increasing the number of functional transcription complexes.

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Year:  1994        PMID: 8264601      PMCID: PMC358383          DOI: 10.1128/mcb.14.1.339-347.1994

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


  75 in total

Review 1.  TATA-binding protein is a classless factor.

Authors:  P A Sharp
Journal:  Cell       Date:  1992-03-06       Impact factor: 41.582

2.  Differential expression of oocyte-type class III genes with fraction TFIIIC from immature or mature oocytes.

Authors:  W F Reynolds; D L Johnson
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

3.  A role for the TATA-box-binding protein component of the transcription factor IID complex as a general RNA polymerase III transcription factor.

Authors:  R J White; S P Jackson; P W Rigby
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-01       Impact factor: 11.205

4.  Gene regulation. Transcriptional transgressions.

Authors:  M R Green
Journal:  Nature       Date:  1992-06-04       Impact factor: 49.962

5.  The phorbol ester, 12-O-tetradecanoylphorbol-13-acetate, induces specific transcription by RNA polymerase III in Drosophila Schneider cells.

Authors:  M Garber; S Panchanathan; R S Fan; D L Johnson
Journal:  J Biol Chem       Date:  1991-11-05       Impact factor: 5.157

Review 6.  RNA polymerase III (C) and its transcription factors.

Authors:  O S Gabrielsen; A Sentenac
Journal:  Trends Biochem Sci       Date:  1991-11       Impact factor: 13.807

7.  The TATA-binding protein is required for transcription by all three nuclear RNA polymerases in yeast cells.

Authors:  B P Cormack; K Struhl
Journal:  Cell       Date:  1992-05-15       Impact factor: 41.582

8.  The mammalian TFIID protein is present in two functionally distinct complexes.

Authors:  H T Timmers; P A Sharp
Journal:  Genes Dev       Date:  1991-11       Impact factor: 11.361

9.  Composition of transcription factor B-TFIID.

Authors:  H T Timmers; R E Meyers; P A Sharp
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-01       Impact factor: 11.205

10.  Coactivators for a proline-rich activator purified from the multisubunit human TFIID complex.

Authors:  N Tanese; B F Pugh; R Tjian
Journal:  Genes Dev       Date:  1991-12       Impact factor: 11.361

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  20 in total

1.  Casein kinase II is required for efficient transcription by RNA polymerase III.

Authors:  D J Hockman; M C Schultz
Journal:  Mol Cell Biol       Date:  1996-03       Impact factor: 4.272

2.  Silkworm TFIIIB binds both constitutive and silk gland-specific tRNA Ala promoters but protects only the constitutive promoter from DNase I cleavage.

Authors:  L S Young; N Ahnert; K U Sprague
Journal:  Mol Cell Biol       Date:  1996-03       Impact factor: 4.272

3.  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

4.  The activity of transcription factor PBP, which binds to the proximal sequence element of mammalian U6 genes, is regulated during differentiation of F9 cells.

Authors:  W Meissner; A Ahlers; K H Seifart
Journal:  Mol Cell Biol       Date:  1995-11       Impact factor: 4.272

5.  Coordinate regulation of ribosomal component synthesis in Acanthamoeba castellanii: 5S RNA transcription is down regulated during encystment by alteration of TFIIIA activity.

Authors:  J L Matthews; M G Zwick; M R Paule
Journal:  Mol Cell Biol       Date:  1995-06       Impact factor: 4.272

6.  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

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.  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

9.  The hepatitis B virus X protein increases the cellular level of TATA-binding protein, which mediates transactivation of RNA polymerase III genes.

Authors:  H D Wang; C H Yuh; C V Dang; D L Johnson
Journal:  Mol Cell Biol       Date:  1995-12       Impact factor: 4.272

10.  Increased expression of TATA-binding protein, the central transcription factor, can contribute to oncogenesis.

Authors:  Sandra A S Johnson; Louis Dubeau; Michael Kawalek; Andrew Dervan; Axel H Schönthal; Chi V Dang; Deborah L Johnson
Journal:  Mol Cell Biol       Date:  2003-05       Impact factor: 4.272

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