The Epithelium-specific ETS Protein EHF/ESE-3 is a Context-dependent Transcriptional Repressor Downstream of MAPK Signaling Cascades

Antonio Tugores, Jennifer Le, Irina Sorokina, A. J. Snijders, Mabel Duyao, P. Sanjeeva Reddy, Leone Carlée, Mathew Ronshaugen, Arcady Mushegian, Tim Watanaskul, Sunny Chu, Alan Buckler, Spencer Emtage, Mary Kay McCormick

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Exon trapping and cDNA selection procedures were used to search for novel genes at human chromosome 11p13, a region previously associated with loss of heterozygosity in epithelial carcinomas. Using these approaches, we found the ESE-2 and ESE-3 genes, coding for ETS domain-containing transcription factors. These genes lie in close proximity to the catalase gene within a ∼200-kilobase genomic interval. ESE-3 mRNA is widely expressed in human tissues with high epithelial content, and immunohistochemical analysis with a newly generated monoclonal antibody revealed that ESE-3 is a nuclear protein expressed exclusively in differentiated epithelial cells and that it is absent in the epithelial carcinomas tested. In transient transfections, ESE-3 behaves as a repressor of the Ras- or phorbol ester-induced transcriptional activation of a subset of promoters that contain ETS and AP-1 binding sites. ESE-3-mediated repression is sequence- and context-dependent and depends both on the presence of high affinity ESE-3 binding sites in combination with AP-1 cis-elements and the arrangement of these sites within a given promoter. We propose that ESE-3 might be an important determinant in the control of epithelial differentiation, as a modulator of the nuclear response to mitogen-activated protein kinase signaling cascades.
    Original languageEnglish
    Pages (from-to)20397-20406
    Number of pages9
    JournalJournal of Biological Chemistry
    Volume276
    Issue number23
    DOIs
    Publication statusPublished - 8 Jun 2001

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