PUBLICATION
The USP46 complex deubiquitylates LRP6 to promote Wnt/β-catenin signaling
- Authors
- Ng, V.H., Spencer, Z., Neitzel, L.R., Nayak, A., Loberg, M.A., Shen, C., Kassel, S.N., Kroh, H.K., An, Z., Anthony, C.C., Bryant, J.M., Lawson, A., Goldsmith, L., Benchabane, H., Hansen, A.G., Li, J., D'Souza, S., Lebensohn, A.M., Rohatgi, R., Weiss, W.A., Weiss, V.L., Williams, C., Hong, C.C., Robbins, D.J., Ahmed, Y., Lee, E.
- ID
- ZDB-PUB-231006-59
- Date
- 2023
- Source
- Nature communications 14: 61736173 (Journal)
- Registered Authors
- Hong, Charles
- Keywords
- none
- MeSH Terms
-
- Animals
- Endopeptidases*/metabolism
- Humans
- Ligases/metabolism
- Low Density Lipoprotein Receptor-Related Protein-6/genetics
- Low Density Lipoprotein Receptor-Related Protein-6/metabolism
- Receptors, Wnt
- Ubiquitin
- Wnt Signaling Pathway*
- Zebrafish/metabolism
- beta Catenin*/genetics
- beta Catenin*/metabolism
- PubMed
- 37798301 Full text @ Nat. Commun.
Citation
Ng, V.H., Spencer, Z., Neitzel, L.R., Nayak, A., Loberg, M.A., Shen, C., Kassel, S.N., Kroh, H.K., An, Z., Anthony, C.C., Bryant, J.M., Lawson, A., Goldsmith, L., Benchabane, H., Hansen, A.G., Li, J., D'Souza, S., Lebensohn, A.M., Rohatgi, R., Weiss, W.A., Weiss, V.L., Williams, C., Hong, C.C., Robbins, D.J., Ahmed, Y., Lee, E. (2023) The USP46 complex deubiquitylates LRP6 to promote Wnt/β-catenin signaling. Nature communications. 14:61736173.
Abstract
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.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping