FBXO42 facilitates Notch signaling activation and global chromatin relaxation by promoting K63-linked polyubiquitination of RBPJ

Author:

Jiang Hua123ORCID,Bian Weixiang123ORCID,Sui Yue123ORCID,Li Huanle23ORCID,Zhao Han23,Wang Wenqi4ORCID,Li Xu123ORCID

Affiliation:

1. Fudan University, Shanghai 310018, China.

2. Key Laboratory of Structural Biology of Zhejiang Province, School of Life Sciences, Westlake University, Hangzhou 310024, Zhejiang, China.

3. Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou 310024, Zhejiang, China.

4. Department of Developmental and Cell Biology, University of California, Irvine, Irvine, CA 92697, USA.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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