Journal Article

The USP46 complex deubiquitylates LRP6 to promote Wnt/β-catenin signaling

Loberg, Matthew A., Hansen, Amanda G., Weiss, William A., Kassel, Sara N., Williams, Charles, An, Zhenyi, Rohatgi, Rajat, D’Souza, Starina, Lee, Ethan, Benchabane, Hassina, Neitzel, Leif R., Shen, Chen, Bryant, Jamal M., Lawson, Amanda, Anthony, Christin C., Hong, Charles C., Spencer, Zachary, Lebensohn, Andres M., Ng, Victoria H., Nayak, Anmada, Ahmed, Yashi, Goldsmith, Lily, Li, Jingjing, Kroh, Heather K., Weiss, Vivian L., Robbins, David J.

2023

Overview

The relative abundance of Wnt receptors plays a crucial role in controlling Wnt signaling in tissue homeostasis and human disease. While the ubiquitin ligases that ubiquitylate Wnt receptors are well-characterized, the deubiquitylase that reverses these reactions remains unclear. Herein, we identify USP46, UAF1, and WDR20 (USP46 complex) as positive regulators of Wnt signaling in cultured human cells. We find that the USP46 complex is similarly required for Wnt signaling in Xenopus and zebrafish embryos. We demonstrate that Wnt signaling promotes the association between the USP46 complex and cell surface Wnt coreceptor, LRP6. Knockdown of USP46 decreases steady-state levels of LRP6 and increases the level of ubiquitylated LRP6. In contrast, overexpression of the USP46 complex blocks ubiquitylation of LRP6 by the ubiquitin ligases RNF43 and ZNFR3. Size exclusion chromatography studies suggest that the size of the USP46 cytoplasmic complex increases upon Wnt stimulation. Finally, we show that USP46 is essential for Wnt-dependent intestinal organoid viability, likely via its role in LRP6 receptor homeostasis. We propose a model in which the USP46 complex increases the steady-state level of cell surface LRP6 and facilitates the assembly of LRP6 into signalosomes via a pruning mechanism that removes sterically hindering ubiquitin chains. Wnt receptors are controlled by their ubiquitin-mediated proteolysis. The authors show that the USP46 deubiquitylase complex potentiates Wnt signaling in human cells, Xenopus , and zebrafish by inhibiting cell surface LRP6 degradation.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 631/80/458/582 / 631/80/86/2368 / 631/80/86/2370 / 64 / 64/114 / 64/116 / 82/29 / 82/80 / 96 / 96/1 / 96/106 / 96/63 / Animals / beta Catenin - genetics / beta Catenin - metabolism / Cell surface / Danio rerio / Embryos / Endopeptidases - metabolism / Homeostasis / Humanities and Social Sciences / Humans / Ligases - metabolism / Low Density Lipoprotein Receptor-Related Protein-6 - genetics / Low Density Lipoprotein Receptor-Related Protein-6 - metabolism / multidisciplinary / Organoids / Proteolysis / Receptors / Receptors, Wnt / Relative abundance / Science / Science (multidisciplinary) / Signalosomes / Size exclusion chromatography / Steady state / Ubiquitin / Wnt protein / Wnt Signaling Pathway / Xenopus / Zebrafish / Zebrafish - metabolism / β-Catenin