The role of a Williams-Beuren syndrome-associated helix–loop–helix domain-containing transcription factor in activin/nodal signaling

  1. Colleen Ring1,3,
  2. Souichi Ogata1,3,
  3. Lauren Meek1,
  4. Jihwan Song1,
  5. Tatsuru Ohta2,
  6. Kohei Miyazono2, and
  7. Ken W.Y. Cho1,4
  1. 1Department of Developmental and Cell Biology, and Developmental Biology Center, University of California, Irvine, California 92697-2300, USA; 2Department of Biochemistry, The Cancer Institute of the Japanese Foundation for Cancer Research (JFCR) Toshima-ku, Tokyo 170–8455, Japan

Abstract

We investigated the regulation of the activin/nodal-inducible distal element (DE) of the Xenopus goosecoid (gsc) promoter. On the basis of its interaction with the DE, we isolated aXenopus homolog of the human Williams-Beuren syndrome critical region 11 (XWBSCR11), and further, show that it interacts with pathway-specific Smad2 and Smad3 in a ligand-dependent manner. Interestingly, we also find that XWBSCR11 functions cooperatively with FoxH1 (Fast-1) to stimulate DE-dependent transcription. We propose a mechanism in which FoxH1 functions together with Smads as a cofactor for the recruitment of transcription factors like XWBSCR11 in the process of activin/nodal-mediated gsc-specific induction. This mechanism provides considerable opportunities for modulation of transcription across a variety of activin/nodal-inducible genes, increasing diversity in promoter selection, thus leading to the differential induction of activin/nodal target genes.

Keywords

Footnotes

  • 3 These authors contributed equally to this work.

  • 4 Corresponding author.

  • E-MAIL kwcho{at}uci.edu; FAX (949) 824-4709.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.963802.

    • Received November 19, 2001.
    • Accepted February 15, 2002.
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