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• W2063315744 abstract "The proteasomal degradation of beta-catenin mediated by the glycogen synthase kinase 3beta (GSK3beta) and destruction complex is the central step in the canonical Wnt signaling pathway. However, that there are branches of Wnt signaling pathways that do not depend on beta-catenin/Tcf-mediated transcription activation has long been understood. In this study, we hypothesized that there are many more GSK3 and destruction complex-dependent proteolytic target proteins that mediate Wnt signaling in the cell. To test this hypothesis, we have developed and carried out a screen for such candidate proteins using an in vitro expression cloning technique and biochemical reconstitution of Wnt signaling in Xenopus egg cytoplasmic extracts. Forty-two proteins have been identified as potential candidates for GSK3-regulated phosphorylation, proteasomal degradation, or both, of which 12 are strong candidates for Wnt-pathway-regulated degradation. Some of them have been reported to interact with beta-catenin and implicated in the canonical Wnt signaling pathway, and other targets identified include proteins with various cellular functions such as RNA processing, cytoskeletal dynamics, and cell metabolism. Thus, we propose that Wnt/GSK3/destruction complex signaling regulates multiple target proteins to control a broad range of cellular activities in addition to beta-catenin-mediated transcription activation." @default.
• W2063315744 created "2016-06-24" @default.
• W2063315744 creator A5014081492 @default.
• W2063315744 creator A5036925508 @default.
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• W2063315744 date "2009-03-31" @default.
• W2063315744 modified "2023-09-30" @default.
• W2063315744 title "Identification of targets of the Wnt pathway destruction complex in addition to β-catenin" @default.
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• W2063315744 doi "https://doi.org/10.1073/pnas.0810185106" @default.
• W2063315744 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2663984" @default.
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• W2063315744 hasPublicationYear "2009" @default.
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