Functional analysis in Drosophila indicates that the NBCCS/PTCH1 mutation G509V results in activation of smoothened through a dominant‐negative mechanism

• Published in: Developmental dynamics Vol. 229; no. 4; pp. 780 - 790
• Main Authors: Hime, Gary R., Lada, Hania, Fietz, Michael J., Gillies, Susan, Passmore, Abraham, Wicking, Carol, Wainwright, Brandon J.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-04-2004
• Subjects: Amino Acid Sequence; Animals; Basal Cell Nevus Syndrome - genetics; Body Patterning; Drosophila; Drosophila - genetics; Drosophila - growth & development; Drosophila - metabolism; Drosophila Proteins; Fluorescent Antibody Technique; Humans; Membrane Proteins - genetics; Membrane Proteins - metabolism; Molecular Sequence Data; Mutation, Missense; NBCCS; patched; Patched Receptors; Patched-1 Receptor; Protein Structure, Tertiary - genetics; Receptors, Cell Surface; Receptors, G-Protein-Coupled - genetics; Receptors, G-Protein-Coupled - metabolism; Salivary Glands - anatomy & histology; Salivary Glands - cytology; Smoothened Receptor; Wings, Animal - anatomy & histology; Wings, Animal - cytology
• ISSN: 1058-8388; 1097-0177
• DOI: 10.1002/dvdy.10499

Mutations in the human homolog of the patched gene are associated with the developmental (and cancer predisposition) condition Nevoid Basal Cell Carcinoma Syndrome (NBCCS), as well as with sporadic basal cell carcinomas. Most mutations that have been identified in the germline of NBCCS patients are truncating or frameshift mutations, with amino acid substitutions rarely found. We show that a missense mutation in the sterol‐sensing domain G509V acts as a dominant negative when assayed in vivo in Drosophila. Ectopic expression of a Drosophila patched transgene, carrying the analogous mutation to G509V, causes ectopic activation of Hedgehog target genes and ectopic membrane stabilisation of Smoothened. The G509V transgene behaves in a manner similar, except in its subcellular distribution, to a C‐terminal truncation that has been characterised previously as a dominant‐negative protein. G509V exhibits vesicular localisation identical to the wild‐type protein, but the C‐terminal truncated Patched molecule is localised predominantly to the plasma membrane. This finding suggests that dominant‐negative function can be conferred by interruption of different aspects of Patched protein behaviour. Another mutation at the same residue, G509R, did not exhibit dominant‐negative activity, suggesting that simple removal of the glycine at 509 is not sufficient to impart dominant‐negative function. Developmental Dynamics 229:780–790, 2004. © 2004 Wiley‐Liss, Inc.