Notch信号通路
染色质
泛素连接酶
细胞生物学
泛素
生物
Hes3信号轴
信号转导
染色质重塑
HEK 293细胞
染色质免疫沉淀
调节器
遗传学
基因
发起人
基因表达
作者
Hua Jiang,Weixiang Bian,Yue Sui,Huanle Li,Han Zhao,Wenqi Wang,Xu Li
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-09-23
卷期号:8 (38)
被引量:6
标识
DOI:10.1126/sciadv.abq4831
摘要
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.
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