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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6900
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pubmed:dateCreated |
2002-8-22
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pubmed:abstractText |
Mutations affecting the transmembrane proteins Patched (Ptc) or Smoothened (Smo) that trigger ligand-independent activity of the Hedgehog (Hh) signalling pathway are associated with human tumours such as basal cell carcinoma (BCC) and medulloblastoma. Despite extensive genetic studies demonstrating the importance of these receptor components in embryonic patterning and cancer, the mechanism by which Ptc regulates Smo is not understood. Here we report that Ptc and Smo are not significantly associated within Hh-responsive cells. Furthermore, we show that free Ptc (unbound by Hh) acts sub-stoichiometrically to suppress Smo activity and thus is critical in specifying the level of pathway activity. Patched is a twelve-transmembrane protein with homology to bacterial proton-driven transmembrane molecular transporters; we demonstrate that the function of Ptc is impaired by alterations of residues that are conserved in and required for function of these bacterial transporters. These results suggest that the Ptc tumour suppressor functions normally as a transmembrane molecular transporter, which acts indirectly to inhibit Smo activity, possibly through changes in distribution or concentration of a small molecule.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Hedgehog Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides...,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, G-Protein-Coupled,
http://linkedlifedata.com/resource/pubmed/chemical/SMO protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Smo protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators,
http://linkedlifedata.com/resource/pubmed/chemical/patched receptors
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0028-0836
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
22
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pubmed:volume |
418
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
892-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12192414-3T3 Cells,
pubmed-meshheading:12192414-Amino Acid Sequence,
pubmed-meshheading:12192414-Animals,
pubmed-meshheading:12192414-Catalysis,
pubmed-meshheading:12192414-Gene Deletion,
pubmed-meshheading:12192414-Hedgehog Proteins,
pubmed-meshheading:12192414-Humans,
pubmed-meshheading:12192414-Intracellular Signaling Peptides and Proteins,
pubmed-meshheading:12192414-Membrane Proteins,
pubmed-meshheading:12192414-Mice,
pubmed-meshheading:12192414-Models, Biological,
pubmed-meshheading:12192414-Mutation, Missense,
pubmed-meshheading:12192414-Receptors, Cell Surface,
pubmed-meshheading:12192414-Receptors, G-Protein-Coupled,
pubmed-meshheading:12192414-Signal Transduction,
pubmed-meshheading:12192414-Syndrome,
pubmed-meshheading:12192414-Trans-Activators,
pubmed-meshheading:12192414-Transfection,
pubmed-meshheading:12192414-Tumor Cells, Cultured
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pubmed:year |
2002
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pubmed:articleTitle |
Patched acts catalytically to suppress the activity of Smoothened.
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pubmed:affiliation |
Howard Hughes Medical Institute, Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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