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Nat Chem Biol September 1, 2013; 9 (9): 557-64.

Oxysterol binding to the extracellular domain of Smoothened in Hedgehog signaling.

Nedelcu D , Liu J , Xu Y , Jao C , Salic A .

Oxysterols bind the seven-transmembrane protein Smo (Smo) and potently activate vertebrate Hedgehog (Hh) signaling, a pathway essential in embryonic development, adult stem cell maintenance and cancer. It is unknown, however, whether oxysterols are important for normal vertebrate Hh signaling and whether antagonizing oxysterols can inhibit the Hh pathway. We developed azasterols that block Hh signaling by binding the oxysterol-binding site of Smo. We show that the binding site for oxysterols and azasterols maps to the extracellular, cysteine-rich domain of Smo and is completely separable from the site bound by other small-molecule modulators, located within the heptahelical bundle of Smo. Smo mutants in which oxysterol binding is abolished no longer respond to oxysterols and cannot be maximally activated by the Hh ligand. Our results show that oxysterol binding to vertebrate Smo is required for normal Hh signaling and that targeting the oxysterol-binding site is an effective strategy to inhibit Smo.

PubMed ID: 23831757
PMC ID: PMC3749252
Article link: Nat Chem Biol
Grant support: [+]
Genes referenced: fzd8 gli1 pnmt sag shh smo wnt3a wnt8a

Article Images: [+] show captions
References [+] :
Aanstad, The extracellular domain of Smoothened regulates ciliary localization and is required for high-level Hh signaling. 2009, Pubmed

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