Structural mechanism for noncanonical GPCR signaling in the Hedgehog pathway

The Hedgehog (Hh) pathway is fundamental to embryogenesis, tissue homeostasis and cancer. Hh signals are transduced through an unusual mechanism; upon agonist-induced phosphorylation, the noncanonical G-protein-coupled receptor (GPCR) Smoothened (SMO) binds the protein kinase A (PKA) catalytic subunit (PKA-C) and physically blocks its enzymatic activity. Here, by combining computational structural approaches with biochemical and functional studies, we show that SMO mimics strategies prevalent in canonical GPCR and PKA signaling complexes, despite little sequence or secondary-structure homology. The intrinsically disordered SMO cytoplasmic domain binds the PKA-C active site, resembling the regulatory subunit within PKA holoenzymes, while the SMO transmembrane domain binds a conserved PKA-C interaction hub. Unlike prevailing GPCR signal transduction models, phosphorylation of SMO promotes intramolecular electrostatic interactions that stabilize structural elements within its cytoplasmic domain, thereby remodeling it into a PKA-inhibiting conformation. Our work provides a structural mechanism for a central step in Hh signaling and defines a principle for disordered GPCR domains to transmit signals intracellularly.

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Publication Details

Journal
Nature Structural & Molecular Biology
Published
2026-04-30
DOI
https://doi.org/10.1038/s41594-026-01800-z
Primary Topic
Hedgehog Signaling Pathway Studies
Type
article
Field-Weighted Citation Impact
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article

Structural mechanism for noncanonical GPCR signaling in the Hedgehog pathway

Friedrich W. Herberg, Jan W. Bröckel, Zachary Michaelson, G Liu et al.
Nature Structural & Molecular Biology
Hedgehog Signaling Pathway Studies
article

Structural mechanism for noncanonical GPCR signaling in the Hedgehog pathway

Friedrich W. Herberg, Jan W. Bröckel, Zachary Michaelson, G Liu, Michael S. Kay, Paul Spaltenstein, Varun Venkatakrishnan, Susan Serota Taylor, Roland L. Dunbrack, Tomasz Maciej Stępniewski, Corvin D. Arveseth, Jana Selent, Jiewei Xu, Nathan Iverson, Benjamin R. Myers, William Steiner, Ganesh S. Anand, Daniela Bertinetti, Ruth Hüttenhain, Erhu Cao, Isaac Nelson, Ju-Fen Zhu, Annabel Lee, Jian Wu, Jessica G H Bruystens, Gerald Tan
article en

Abstract

The Hedgehog (Hh) pathway is fundamental to embryogenesis, tissue homeostasis and cancer. Hh signals are transduced through an unusual mechanism; upon agonist-induced phosphorylation, the noncanonical G-protein-coupled receptor (GPCR) Smoothened (SMO) binds the protein kinase A (PKA) catalytic subunit (PKA-C) and physically blocks its enzymatic activity. Here, by combining computational structural approaches with biochemical and functional studies, we show that SMO mimics strategies prevalent in canonical GPCR and PKA signaling complexes, despite little sequence or secondary-structure homology. The intrinsically disordered SMO cytoplasmic domain binds the PKA-C active site, resembling the regulatory subunit within PKA holoenzymes, while the SMO transmembrane domain binds a conserved PKA-C interaction hub. Unlike prevailing GPCR signal transduction models, phosphorylation of SMO promotes intramolecular electrostatic interactions that stabilize structural elements within its cytoplasmic domain, thereby remodeling it into a PKA-inhibiting conformation. Our work provides a structural mechanism for a central step in Hh signaling and defines a principle for disordered GPCR domains to transmit signals intracellularly.

Nature Structural & Molecular Biology
University of Kassel (DE), Fox Chase Cancer Center (US), Pennsylvania State University (US), Universitat Pompeu Fabra (ES), Duke University (US), University of California, San Francisco (US), Washington University in St. Louis (US), University of Utah (US), Huntsman Cancer Institute (US), University of California San Diego (US), Stanford University (US)
Openalex Percentile: Top 12%
Hedgehog Signaling Pathway Studies
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