Scube/You activity mediates release of dually lipid-modified Hedgehog signal in soluble form

  1. Philip A. Beachy1,2,3,4,5
  1. 1Institute for Stem Cell Biology and Regenerative Medicine,
  2. 2Department of Developmental Biology, Stanford University, Stanford, California 94305, USA;
  3. 3Department of Molecular Biology and Genetics, The Johns Hopkins Medical Institutions, Baltimore, Maryland 21205, USA;
  4. 4Department of Biochemistry, Stanford University, Stanford, California 94305, USA

    Abstract

    Owing to their covalent modification by cholesterol and palmitate, Hedgehog (Hh) signaling proteins are localized predominantly to the plasma membrane of expressing cells. Yet Hh proteins are also capable of mobilizing to and eliciting direct responses from distant cells. The zebrafish you gene, identified genetically >15 years ago, was more recently shown to encode a secreted glycoprotein that acts cell-nonautonomously in the Hh signaling pathway by an unknown mechanism. We investigated the function of the protein encoded by murine Scube2, an ortholog of you, and found that it mediates release in soluble form of the mature, cholesterol- and palmitate-modified Sonic hedgehog protein signal (ShhNp) when added to cultured cells or purified detergent-resistant membrane microdomains containing ShhNp. The efficiency of Scube2-mediated release of ShhNp is enhanced by the palmitate adduct of ShhNp and by coexpression in ShhNp-producing cells of mDispatchedA (mDispA), a transporter-like protein with a previously defined role in the release of lipid-modified Hh signals. The structural determinants of Scube2 required for its activity in cultured cell assays match those required for rescue of you mutant zebrafish embryos, and we thus conclude that the role of Scube/You proteins in Hh signaling in vivo is to facilitate the release and mobilization of Hh proteins for distant action.

    Keywords

    Footnotes

    • Received March 12, 2012.
    • Accepted May 9, 2012.

    Freely available online through the Genes & Development Open Access option.

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