USP35 dimer prevents its degradation by E3 ligase CHIP through auto-deubiquitinating activity
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00018-023-04740-9.pdf
Reference32 articles.
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2. Leznicki P, Natarajan J, Bader G, Spevak W, Schlattl A et al (2018) Expansion of DUB functionality generated by alternative isoforms—USP35, a case study. J Cell Sci. https://doi.org/10.1242/jcs.212753
3. Park J, Kwon MS, Kim EE, Lee H, Song EJ (2018) USP35 regulates mitotic progression by modulating the stability of Aurora B. Nat Commun 9:688. https://doi.org/10.1038/s41467-018-03107-0
4. Tsai IC, Adams KA, Tzeng JA, Shennib O, Tan PL et al (2019) Genome-wide suppressor screen identifies USP35/USP38 as therapeutic candidates for ciliopathies. JCI Insight 4:e130516. https://doi.org/10.1172/jci.insight.130516
5. Cao J, Wu D, Wu G, Wang Y, Ren T et al (2021) USP35, regulated by estrogen and AKT, promotes breast tumorigenesis by stabilizing and enhancing transcriptional activity of estrogen receptor alpha. Cell Death Dis 12:619. https://doi.org/10.1038/s41419-021-03904-4
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2. Friend or foe? Reciprocal regulation between E3 ubiquitin ligases and deubiquitinases;Biochemical Society Transactions;2024-02-28
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