The human eps15 gene, encoding a tyrosine kinase substrate, is conserved in evolution and maps to Ip31-p32

William T. Wong, Matthias H. Kraus, Francesca Carlomagno, Alexandra Zelano, Teresa Druck, Carlo M. Croce, Kay Huebner, Pier Paolo Di Fiore

Research output: Contribution to journalArticlepeer-review


Employing an expression cloning approach for tyrosine kinase substrates, we have previously isolated the coding sequence for a novel putative EGFR substrate, eps15, from NIH3T3 fibroblasts. Eps15 displayed a receptor-specific pattern of tyrosine phosphorylation in vivo and was able to transform NIH3T3 cells upon overexpression. To gain understanding of eps15 function as well as its role in normal and neoplastic proliferation, we cloned the human eps15 coding sequence and studied expression of the human RNA and protein, evolutionary conservation, and chromosomal location. The close structural similarity of human eps15 with the murine homologue is indicated by 89% and 90% identity of nucleotide and predicted amino acid sequences, respectively. Using the human eps15 coding sequence as probe, we demonstrate that eps15 is member of a gene family that is highly conserved during evolution. An essential function of eps15 in cell growth regulation is underscored by our observation of ubiquitous expression at the transcript and the protein level in normal and malignant human cells. The human EPS15 locus maps to chromosome Ip31-p32, a region involved in deletion in neuroblastoma, translocations in acute lymphoblastic leukemia, and exhibiting a fragile site.

Original languageEnglish
Pages (from-to)1591-1597
Number of pages7
Issue number6
Publication statusPublished - Jun 1994

ASJC Scopus subject areas

  • Cancer Research
  • Genetics
  • Molecular Biology


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