학술논문

Genome-wide identification of phospho-regulators of Wnt signaling in Drosophila.
Document Type
Academic Journal
Author
Swarup S; Simon Fraser University, Department of Molecular Biology and Biochemistry, Burnaby V5A1S6, British Columbia, Canada.; Pradhan-Sundd T; Simon Fraser University, Department of Molecular Biology and Biochemistry, Burnaby V5A1S6, British Columbia, Canada.; Verheyen EM; Simon Fraser University, Department of Molecular Biology and Biochemistry, Burnaby V5A1S6, British Columbia, Canada everheye@sfu.ca.
Source
Publisher: Company Of Biologists Limited Country of Publication: England NLM ID: 8701744 Publication Model: Print Cited Medium: Internet ISSN: 1477-9129 (Electronic) Linking ISSN: 09501991 NLM ISO Abbreviation: Development Subsets: MEDLINE
Subject
Language
English
Abstract
Evolutionarily conserved intercellular signaling pathways regulate embryonic development and adult tissue homeostasis in metazoans. The precise control of the state and amplitude of signaling pathways is achieved in part through the kinase- and phosphatase-mediated reversible phosphorylation of proteins. In this study, we performed a genome-wide in vivo RNAi screen for kinases and phosphatases that regulate the Wnt pathway under physiological conditions in the Drosophila wing disc. Our analyses have identified 54 high-confidence kinases and phosphatases capable of modulating the Wnt pathway, including 22 novel regulators. These candidates were also assayed for a role in the Notch pathway, and numerous phospho-regulators were identified. Additionally, each regulator of the Wnt pathway was evaluated in the wing disc for its ability to affect the mechanistically similar Hedgehog pathway. We identified 29 dual regulators that have the same effect on the Wnt and Hedgehog pathways. As proof of principle, we established that Cdc37 and Gilgamesh/CK1γ inhibit and promote signaling, respectively, by functioning at analogous levels of these pathways in both Drosophila and mammalian cells. The Wnt and Hedgehog pathways function in tandem in multiple developmental contexts, and the identification of several shared phospho-regulators serve as potential nodes of control under conditions of aberrant signaling and disease.
(© 2015. Published by The Company of Biologists Ltd.)