A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Malpel, S., Claret, S., Sanial, M., Brigui, A., Piolot, T., Daviet, L., Martin-Lanneree, S., Plessis, A. (2007). The last 59 amino acids of Smoothened cytoplasmic tail directly bind the protein kinase Fused and negatively regulate the Hedgehog pathway.  Dev. Biol. 303(1): 121--133. (Export to RIS)
FlyBase ID FBrf0194316
Publication Type Research paper
PubMed ID 17182028
PubMed Abstract The Hedgehog (HH) signaling pathway is crucial for the development of many organisms and its inappropriate activation is involved in numerous cancers. HH signal controls the traffic and activity of the seven-pass transmembrane protein Smoothened (SMO), leading to the transcriptional regulation of HH-responsive genes. In Drosophila, the intracellular transduction events following SMO activation depend on cytoplasmic multimeric complexes that include the Fused (FU) protein kinase. Here we show that the regulatory domain of FU physically interacts with the last 52 amino acids of SMO and that the two proteins colocalize in vivo to vesicles. The deletion of this region of SMO leads to a constitutive activation of SMO, promoting the ectopic transcription of HH target genes. This activation is partially dependent of FU activity. Thus, we identify a novel link between SMO and the cytoplasmic complex(es) and reveal a negative role of the SMO C-terminal region that interacts with FU. We propose that FU could act as a switch, activator in presence of HH signal or inhibitor in absence of HH.
DOI 10.1016/j.ydbio.2006.10.042
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Language of Publication English
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Publication Type Journal
Abbreviation Dev. Biol.
Title Developmental Biology
Publication Year 1959-
ISBN/ISSN 0012-1606
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