Dependence of lymphopoiesis on efficient β-catenin degradation

Abstract

Abstract Wnt/β-catenin pathway is tightly controlled by β-catenin destruction complex to regulate lineage specification and differentiation. Compared to epithelial lineage, lymphoid cells display higher rates of β-catenin degradation to achieve constitutively low levels of β-catenin. Emphasizing the reliance of lymphoid cells on β-catenin degradation, expression of degradation resistant form of β-catenin or deletion of APC or CK1 suppressed lymphoid development. Similarly, small molecules inhibiting GSK3β mediated phosphorylation or proteasomal degradation of β-catenin induced higher toxicity selectively in lymphoid cells compared to other lineages. Our interactome and CHIP-seq analysis highlighted that the unique dependency of lymphoid cells on efficient degradation of β-catenin is mediated by Ikaros zinc finger (IKZF) proteins and nucleosome remodeling and deacetylase (NuRD) complexes. Unlike activating TCF/β-catenin complexes in epithelial cells, recruitment of repressive β-catenin/IKZF/NuRD complexes to MYC superenhancer (SE) regions lead to suppression of Myc expression and induced cell death. Deletion of both IKZF1 and IKZF3 or mutation of Ikaros binding motifs within the Myc-SE subverted the β-catenin mediated toxicity. Upon loss of Ikaros factors, β-catenin interaction with TCF-factors resulted in de novo activation of epithelial specific genes. Our findings suggest that β-catenin degradation is an evolutionary requirement for Ikaros mediated protection of lymphoid identity.