The seven-transmembrane-spanning receptors of the FZD1-10 class are bound and activated by the WNT family of lipoglycoproteins, thereby inducing a complex network of signaling pathways. However, the specificity of the interaction between mammalian WNT and FZD proteins and the subsequent signaling cascade downstream of the different WNT-FZD pairs have not been systematically addressed to date. In this study, we determined the binding affinities of various WNTs for different members of the FZD family by using bio-layer interferometry and characterized their functional selectivity in a cell system. Using purified WNTs, we show that different FZD cysteine-rich domains prefer to bind to distinct WNTs with fast on-rates and slow off-rates. In a 32D cell-based system engineered to overexpress FZD2, FZD4, or FZD5, we found that WNT-3A (but not WNT-4, -5A, or -9B) activated the WNT-β-catenin pathway through FZD2/4/5 as measured by phosphorylation of LRP6 and β-catenin stabilization. Surprisingly, different WNT-FZD pairs showed differential effects on phosphorylation of DVL2 and DVL3, revealing a previously unappreciated DVL isoform selectivity by different WNT-FZD pairs in 32D cells. In summary, we present extensive mapping of WNT-FZD cysteine-rich domain interactions complemented by analysis of WNT-FZD pair functionality in a unique cell system expressing individual FZD isoforms. Differential WNT-FZD binding and selective functional readouts suggest that endogenous WNT ligands evolved with an intrinsic natural bias toward different downstream signaling pathways, a phenomenon that could be of great importance in the design of FZD-targeting drugs.

From the Section of Receptor Biology and Signaling Department of Physiology and Pharmacology Karolinska Institutet S 171 77 Stockholm Sweden the Faculty of Science Institute of Experimental Biology Masaryk University 611 37 Brno Czech Republic

From the Section of Receptor Biology and Signaling Department of Physiology and Pharmacology Karolinska Institutet S 171 77 Stockholm Sweden the Laboratory of Cellular and Molecular Biology Center for Cancer Research NCI National Institutes of Health Bethesda Maryland 20892

the Department of Early Discovery Biochemistry Genentech South San Francisco California 94080 and

the Laboratory of Cellular and Molecular Biology Center for Cancer Research NCI National Institutes of Health Bethesda Maryland 20892

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Targeting Casein Kinase 1 (CK1) in Hematological Cancers

WNT5A: a motility-promoting factor in Hodgkin lymphoma

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