Synergistic cooperation of TFE3 and Smad proteins in TGF-β-induced transcription of the plasminogen activator inhibitor-1 gene

  1. Xianxin Hua1,
  2. Xuedong Liu1,
  3. Dominic O. Ansari1, and
  4. Harvey F. Lodish1,2,3
  1. 1The Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142 USA; 2Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 USA

Abstract

Members of the TGF-β superfamily influence a broad range of biological activities including stimulation of wound healing and inhibition of cell growth. TGF-β signals through type I and II receptor serine/ threonine kinases and induces transcription of many genes including plasminogen activator inhibitor-1 (PAI-1). To identify proteins that participate in TGF-β-induced gene expression, we developed a novel retrovirus-mediated expression cloning strategy; and using this approach, we established that transcription factor μE3 (TFE3) is involved in TGF-β-induced activation of the PAI-1 promoter. We showed that TFE3 binds to an E-box sequence in PE2, a 56-bp promoter fragment of the PAI-1 promoter, and that mutation of this sequence abolishes both TFE3 binding as well as TGF-β-dependent activation. TFE3 and Smad3 synergistically activate the PE2 promoter and phosphorylated Smad3 and Smad4 bind to a sequence adjacent to the TFE3-binding site in this promoter. Binding of both TFE3 and the Smad proteins to their cognate sequences is indispensable for TGF-β-inducible activation of the PE2 promoter. Hence, TFE3 is an important transcription factor in at least one TGF-β-activated signal transduction pathway.

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Footnotes

  • 3 Corresponding author.

  • E-MAIL lodish{at}wi.mit.edu; FAX (617) 258-6768.

    • Received June 25, 1998.
    • Accepted August 5, 1998.
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