Literature DB >> 1662987

Differential regulation of jun family gene expression by the tumor promoter okadaic acid.

A Schönthal1, A S Alberts, J A Frost, J R Feramisco.   

Abstract

Phosphorylation events are major regulatory mechanisms of signal transduction pathways that control cell growth and differentiation. The potential involvement of serine/threonine-specific phosphoprotein phosphatases in pathways that regulate gene expression was analyzed. By use of okadaic acid, an inhibitor of protein phosphatases 1 (PP-1) and 2A (PP-2A), we present evidence that expression of distinct members of the jun family of genes, c-jun, junB, and junD, are regulated differentially by serine/threonine-specific phosphoprotein phosphatases. Treatment of cells with okadaic acid induces the expression of junB, and to a lesser extent c-jun, but has only a marginal effect on junD expression. This induction involves transcriptional as well as post-transcriptional mechanisms. An analysis of defined elements in different promoters suggests that serine/threonine phosphoprotein phosphatases are involved in the regulation of the c-jun and the collagenase 12-O-tetradecanoyl phorbol-13-acetate (TPA) response element (TRE) as well as the c-fos serum response element (SRE). Since inhibition of PP-1 and PP-2A leads to increased proto-oncogene expression, our results further support the view that certain protein phosphatases might act as negative regulators of growth.

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Year:  1991        PMID: 1662987

Source DB:  PubMed          Journal:  New Biol        ISSN: 1043-4674


  7 in total

1.  Induction of c-jun protooncogene expression and transcription factor AP-1 activity by the polyoma virus middle-sized tumor antigen.

Authors:  A Schönthal; S Srinivas; W Eckhart
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-01       Impact factor: 11.205

2.  Expression of the tumor necrosis factor alpha gene and early response genes by nodularin, a liver tumor promoter, in primary cultured rat hepatocytes.

Authors:  E Sueoka; N Sueoka; S Okabe; T Kozu; A Komori; T Ohta; M Suganuma; S J Kim; I K Lim; H Fujiki
Journal:  J Cancer Res Clin Oncol       Date:  1997       Impact factor: 4.553

3.  The protein phosphatase inhibitor okadaic acid suppresses type I collagen gene expression in cultured fibroblasts at the transcriptional level.

Authors:  J Westermarck; E Ilvonen; V M Kähäri
Journal:  Biochem J       Date:  1995-06-15       Impact factor: 3.857

4.  Protein phosphatase 2A potentiates activity of promoters containing AP-1-binding elements.

Authors:  A S Alberts; T Deng; A Lin; J L Meinkoth; A Schönthal; M C Mumby; M Karin; J R Feramisco
Journal:  Mol Cell Biol       Date:  1993-04       Impact factor: 4.272

5.  Increase of labeling indices in gastrointestinal mucosae of mice and rats by compounds of the okadaic acid type.

Authors:  H Yuasa; K Yoshida; H Iwata; H Nakanishi; M Suganuma; M Tatematsu
Journal:  J Cancer Res Clin Oncol       Date:  1994       Impact factor: 4.553

6.  c-fos transcriptional activation and repression correlate temporally with the phosphorylation status of TCF.

Authors:  R Zinck; R A Hipskind; V Pingoud; A Nordheim
Journal:  EMBO J       Date:  1993-06       Impact factor: 11.598

7.  Protein phosphatase activity is required for light-inducible gene expression in maize.

Authors:  J Sheen
Journal:  EMBO J       Date:  1993-09       Impact factor: 11.598

  7 in total

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