McKenna Joseph K, Wu Yalan, Sonkusre Praveen, Sinclear Caleb K, Chari Raj, Lebensohn Andres M
Laboratory of Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Genome Modification Core, Laboratory Animal Sciences Program, Frederick National Lab for Cancer Research, Frederick, Maryland, United States of America.
PLoS Genet. 2025 May 27;21(5):e1011677. doi: 10.1371/journal.pgen.1011677. eCollection 2025 May.
WNT/β-catenin signaling is mediated by the transcriptional coactivator β-catenin (CTNNB1). CTNNB1 abundance is regulated by phosphorylation and proteasomal degradation, promoted by a destruction complex composed of the scaffold proteins APC and AXIN1 or AXIN2, and the kinases casein kinase 1α (CSNK1A1) and GSK3A or GSK3B. Loss of CSNK1A1 increases CTNNB1 abundance, resulting in hyperactive WNT signaling. Previously, we demonstrated that the HECT domain E3 ubiquitin ligase HUWE1 is necessary for hyperactive WNT signaling in HAP1 haploid human cells lacking CSNK1A1. Here, we investigated the mechanism underlying this requirement. In HAP1 cells lacking CSNK1A1, GSK3A/GSK3B still phosphorylated a fraction of CTNNB1, promoting its degradation. HUWE1 loss enhanced GSK3A/GSK3B-dependent CTNNB1 phosphorylation, further reducing CTNNB1 abundance. However, the reduction in CTNNB1 caused by HUWE1 loss was smaller than the reduction in WNT target gene transcription. To test whether the reduction in WNT signaling caused by HUWE1 loss resulted from reduced CTNNB1 alone, we engineered the endogenous CTNNB1 locus in HAP1 cells to encode a CTNNB1 variant insensitive to destruction complex-mediated phosphorylation and degradation. HUWE1 loss in these cells did not change CTNNB1 abundance but still reduced WNT signaling, demonstrating that another mechanism was at play. Genetic interaction and overexpression analyses revealed that the reduction in WNT signaling caused by HUWE1 loss required not only GSK3A or GSK3B, but also APC and AXIN1. Therefore, in HAP1 cells lacking CSNK1A1, a residual destruction complex containing APC, AXIN1 and GSK3A or GSK3B downregulates WNT signaling by phosphorylating and targeting CTNNB1 for degradation, and HUWE1 enhances WNT signaling by antagonizing this activity. Regulation of WNT signaling by HUWE1 also requires its ubiquitin ligase activity. We conclude that HUWE1 enhances WNT/CTNNB1 signaling through two mechanisms, one that antagonizes destruction complex-mediated CTNNB1 degradation and another that is independent of changes in CTNNB1 abundance. Coordinated regulation of CTNNB1 abundance and a second signaling step by HUWE1 would be an efficient way to control WNT signaling output, enabling sensitive and robust activation of the pathway.
WNT/β-连环蛋白信号传导由转录共激活因子β-连环蛋白(CTNNB1)介导。CTNNB1的丰度受磷酸化和蛋白酶体降解调节,由支架蛋白APC和AXIN1或AXIN2以及酪蛋白激酶1α(CSNK1A1)和GSK3A或GSK3B组成的破坏复合物促进其降解。CSNK1A1的缺失会增加CTNNB1的丰度,导致WNT信号过度激活。此前,我们证明在缺乏CSNK1A1的HAP1单倍体人类细胞中,HECT结构域E3泛素连接酶HUWE1是WNT信号过度激活所必需的。在此,我们研究了这种需求背后的机制。在缺乏CSNK1A1的HAP1细胞中,GSK3A/GSK3B仍能磷酸化一部分CTNNB1,促进其降解。HUWE1的缺失增强了GSK3A/GSK3B依赖的CTNNB1磷酸化,进一步降低了CTNNB1的丰度。然而,HUWE1缺失导致的CTNNB1减少幅度小于WNT靶基因转录的减少幅度。为了测试HUWE1缺失导致的WNT信号减少是否仅由CTNNB1减少引起,我们对HAP1细胞中的内源性CTNNB1基因座进行改造,使其编码一种对破坏复合物介导的磷酸化和降解不敏感的CTNNB1变体。这些细胞中HUWE1的缺失并没有改变CTNNB1的丰度,但仍然降低了WNT信号,表明还有另一种机制在起作用。遗传相互作用和过表达分析表明,HUWE1缺失导致的WNT信号减少不仅需要GSK3A或GSK3B,还需要APC和AXIN1。因此,在缺乏CSNK1A1的HAP1细胞中,一个包含APC、AXIN1和GSK3A或GSK3B的残余破坏复合物通过磷酸化并靶向CTNNB1进行降解来下调WNT信号,而HUWE1通过拮抗这种活性来增强WNT信号。HUWE1对WNT信号的调节也需要其泛素连接酶活性。我们得出结论,HUWE1通过两种机制增强WNT/CTNNB1信号,一种是拮抗破坏复合物介导的CTNNB1降解,另一种与CTNNB1丰度的变化无关。HUWE1对CTNNB1丰度和第二个信号步骤的协同调节将是控制WNT信号输出的有效方式,能够实现该通路的敏感而稳健的激活。