Further characterisation of the p53 responsive element - identification of new candidate genes for trans-activation by p53

Jean-Christophe Bourdon, Valérie Deguin-Chambon, Jean-Claude Lelong, Philippe Dessen, Pierre May, Brigitte Debuire, Evelyne May

    Research output: Contribution to journalArticlepeer-review

    142 Citations (Scopus)

    Abstract

    The p53 protein is known to trans-activate a number of genes by specific binding to a consensus sequence containing two decamers of the type: PuPuPuCA/TT/AGPyPyPy. In order to identify new p53 trans-activated genes, we defined a set of criteria for computer search of p53-responsive elements, Based on experimental data, we proposed an extended consensus sequence composed of the two decamers of the El-Deiry consensus sequence flanked by two additional ones, A maximum of 3 bp substitutions was accepted for the two decamers of the El-Deiry consensus sequence, as well as for each additional decamer, except when the two decamers of the El-Deiry consensus sequence are contiguous, In this case, each additional decamer is allowed to bear one base insertion or deletion between the median C and G, This set of criteria was validated by identifying within the promoter region of the IGF-BP3 gene the existence of a novel p53-responsive element whose functional significance was verified, By limiting our computer search to Vertebrate genes involved in cell cycle regulation, cellular adhesion or metastatic processes and to gene families most often found in HOVERGEN database, 7785 gene sequences were first analysed, Among the oncogenes, kinases, proteases and structural proteins, 55 new genes were selected; six of them were retrieved in more than one species

    Original languageEnglish
    Pages (from-to)85-94
    Number of pages10
    JournalOncogene
    Volume14
    Issue number1
    Publication statusPublished - 1997

    Fingerprint

    Dive into the research topics of 'Further characterisation of the p53 responsive element - identification of new candidate genes for trans-activation by p53'. Together they form a unique fingerprint.

    Cite this