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Smoothened Goes Molecular: New Pieces in the Hedgehog Signaling Puzzle

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 290, Issue 6, Pages 3500-3507

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.R114.617936

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Funding

  1. National Institutes of Health [R01 HD055545]
  2. National Science Foundation [NSF DGE-1232825]

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A general aim of studies of signal transduction is to identify mediators of specific signals, order them into pathways, and understand the nature of interactions between individual components and how these interactions alter pathway behavior. Despite years of intensive study and its central importance to animal development and human health, our understanding of the Hedgehog (Hh) signaling pathway remains riddled with gaps, question marks, assumptions, and poorly understood connections. In particular, understanding how interactions between Hh and Patched (Ptc), a 12-pass integral membrane protein, lead to modulation of the function of Smoothened (Smo), a 7-pass integral membrane protein, has defied standard biochemical characterization. Recent structural and biochemical characterizations of Smoothened domains have begun to unlock this riddle, however, and lay the groundwork for improved cancer therapies.

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