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Roles of individual human Dishevelled paralogs in the Wnt signalling pathways
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SYSNO ASEP 0546703 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Roles of individual human Dishevelled paralogs in the Wnt signalling pathways Author(s) Paclíková, P. (CZ)
Radaszkiewicz, T.W. (CZ)
Potěšil, D. (CZ)
Harnoš, J. (CZ)
Zdráhal, Z. (CZ)
Bryja, Vítězslav (BFU-R) RID, ORCIDNumber of authors 6 Article number 110058 Source Title Cellular Signalling. - : Elsevier - ISSN 0898-6568
Roč. 85, SEP 2021 (2021)Number of pages 11 s. Publication form Online - E Language eng - English Country NL - Netherlands Keywords gene family ; mechanisms ; axin ; phosphorylation ; activate ; driven Subject RIV EA - Cell Biology OECD category Cell biology Method of publishing Limited access Institutional support BFU-R - RVO:68081707 UT WOS 000685349100004 EID SCOPUS 85108143823 DOI 10.1016/j.cellsig.2021.110058 Annotation Dishevelled (DVL) proteins are key mediators of most Wnt pathways. In all vertebrates, three DVL paralogs are present (DVL1, DVL2 and DVL3) but it is poorly defined to what extent they are functionally redundant. Here, we generated T-REx HEK 293 cells with only one DVL paralog (i.e., DVL1-only, DVL2-only, and DVL3-only) and compared their response to Wnt-3a and Wnt-5a ligands with wild type and DVL triple knockout cells. We show that DVL is essential, in addition to the previously shown Wnt-3a-induced phosphorylation of LRP6 and transcriptional activation of TCF/LEF-dependent reporter, also for Wnt-3a-induced degradation of AXIN1 and Wnt5a-induced phosphorylation of ROR1. We have quantified the molar ratios of DVL1:DVL2:DVL3 in our model to be approximately 4:80:16. Interestingly, DVL-only cells do not compensate for the lack of other paralogs and are still fully functional in all analyzed readouts with the exception of Wnt-3a-induced transcription assessed by TopFlash assay. In this assay, the DVL1-only cell line was the most potent, on the contrary, the DVL3-only cell line exhibited only the negligible capacity to mediate Wnt signals. Using a novel model system complementation assays in T-REx HEK 293 with amplified Wnt signal response (RNF43/ZNRF3/DVL1/DVL2/DVL3 penta KO cells) we demonstrate that it is not the total amount of DVL but ratio of individual paralogs what decides the signal strength. In sum, this study contributes to our better understanding of the role of individual human DVL paralogs in the Wnt pathway. Workplace Institute of Biophysics Contact Jana Poláková, polakova@ibp.cz, Tel.: 541 517 244 Year of Publishing 2022 Electronic address https://www.sciencedirect.com/science/article/pii/S0898656821001479?via%3Dihub
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