Literature DB >> 9556576

The p53 tumor suppressor inhibits transcription of the TATA-less mouse DP1 promoter.

R V Gopalkrishnan1, E W Lam, C Kedinger.   

Abstract

Cell cycle progression is subject to several regulatory controls, of which the p53 protein plays a major role in growth arrest, subsequent to the detection of cellular aberrations. It is well documented that p53 has the ability to inhibit transcription driven by several promoters, possibly via distinct mechanisms. In this report, we show that expression of the cell cycle regulatory transcription factor DP1 is strongly inhibited by p53, at the level of transcription and probably through the basal TATA-less promoter. This inhibitory activity has a relative specificity for the DP1 promoter compared with the functionally related E2F1 promoter or unrelated promoters such as those of the transcription factor ATFa or the thymidine kinase gene. Inhibition of DP1 transcription has implications in one of the several possible mechanisms through which p53 induces cell cycle arrest.

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Year:  1998        PMID: 9556576     DOI: 10.1074/jbc.273.18.10972

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  5 in total

1.  Redefining the p53 response element.

Authors:  Bei Wang; Ziwei Xiao; Ee Chee Ren
Journal:  Proc Natl Acad Sci U S A       Date:  2009-07-13       Impact factor: 11.205

2.  p53 regulates a G2 checkpoint through cyclin B1.

Authors:  S A Innocente; J L Abrahamson; J P Cogswell; J M Lee
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

3.  Transcriptional repression by wild-type p53 utilizes histone deacetylases, mediated by interaction with mSin3a.

Authors:  M Murphy; J Ahn; K K Walker; W H Hoffman; R M Evans; A J Levine; D L George
Journal:  Genes Dev       Date:  1999-10-01       Impact factor: 11.361

4.  Tumor suppressor p53 is required to modulate BRCA1 expression.

Authors:  P Arizti; L Fang; I Park; Y Yin; E Solomon; T Ouchi; S A Aaronson; S W Lee
Journal:  Mol Cell Biol       Date:  2000-10       Impact factor: 4.272

5.  Induction of PPM1D following DNA-damaging treatments through a conserved p53 response element coincides with a shift in the use of transcription initiation sites.

Authors:  Matteo Rossi; Oleg N Demidov; Carl W Anderson; Ettore Appella; Sharlyn J Mazur
Journal:  Nucleic Acids Res       Date:  2008-11-10       Impact factor: 16.971

  5 in total

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