FBXO42 facilitates Notch signaling activation and global chromatin relaxation by promoting K63-linked polyubiquitination of RBPJ.
Hua JiangWeixiang BianYue SuiHuanle LiHan ZhaoWenqi WangXu LiPublished in: Science advances (2022)
Dysregulation of the Notch-RBPJ (recombination signal-binding protein of immunoglobulin kappa J region) signaling pathway has been found associated with various human diseases including cancers; however, precisely how this key signaling pathway is fine-tuned via its interactors and modifications is still largely unknown. In this study, using a proteomic approach, we identified F-box only protein 42 (FBXO42) as a previously unidentified RBPJ interactor. FBXO42 promotes RBPJ polyubiquitination on lysine-175 via lysine-63 linkage, which enhances the association of RBPJ with chromatin remodeling complexes and induces a global chromatin relaxation. Genetically depleting FBXO42 or pharmacologically targeting its E3 ligase activity attenuates the Notch signaling-related leukemia development in vivo. Together, our findings not only revealed FBXO42 as a critical regulator of the Notch pathway by modulating RBPJ-dependent global chromatin landscape changes but also provided insights into the therapeutic intervention of the Notch pathway for leukemia treatment.
Keyphrases
- transcription factor
- signaling pathway
- dna damage
- binding protein
- genome wide
- gene expression
- cell proliferation
- pi k akt
- acute myeloid leukemia
- endothelial cells
- bone marrow
- randomized controlled trial
- epithelial mesenchymal transition
- single cell
- dna repair
- dna methylation
- single molecule
- amino acid
- oxidative stress
- induced apoptosis
- immune response
- combination therapy
- hepatitis c virus
- young adults
- pluripotent stem cells
- label free
- endoplasmic reticulum stress