Laboratory of Molecular and Cellular Cancer Biology, Azrieli Faculty of Medicine, Bar-Ilan University, 1311502, Safed, Israel.
Department of Pathology and Laboratory Medicine, IRCCS Fondazione, Istituto Nazionale dei Tumori, Milan, Italy.
Cell Mol Life Sci. 2022 Apr 11;79(5):237. doi: 10.1007/s00018-022-04272-8.
Epitranscriptomic changes in RNA catalyzed by the RNA-editing enzyme ADAR1 play an essential role in the regulation of diverse molecular and cellular processes, both under physiological conditions and in disease states, including cancer. Yet, despite a growing body of evidence pointing to ADAR1 as a potential therapeutic target, the mechanisms regulating its cellular abundance and activity, particularly of its constitutively expressed and ubiquitous form, ADAR1p110, are poorly understood. Here, we report the HECT-type E3 ubiquitin ligase SMURF2 as a pivotal regulator of ADAR1p110. We show that SMURF2, which is primarily known to promote the ubiquitin-mediated degradation of its protein substrates, protects ADAR1p110 from proteolysis and promotes its A-to-I editase activity in human and mouse cells and tissues. ADAR1p110's interactome analysis performed in human cells also showed a positive influence of SMURF2 on the stability and function of ADAR1p110. Mechanistically, we found that SMURF2 directly binds, ubiquitinates and stabilizes ADAR1p110 in an E3 ubiquitin ligase-dependent manner, through ADAR1p110 ubiquitination at lysine-744 (K744). Mutation of this residue to arginine (K744R), which is also associated with several human disorders, including dyschromatosis symmetrica hereditaria (DSH) and some types of cancer, abolished SMURF2-mediated protection of ADAR1p110 from both proteasomal and lysosomal degradation and inactivated ADAR1p110-mediated RNA editing. Our findings reveal a novel mechanism underlying the regulation of ADAR1 in mammalian cells and suggest SMURF2 as a key cellular factor influencing the protein abundance, interactions and functions of ADAR1p110.
RNA 编辑酶 ADAR1 催化的 RNA 表转录组变化在生理条件和疾病状态(包括癌症)下调节多种分子和细胞过程中发挥着重要作用。然而,尽管越来越多的证据表明 ADAR1 是一种潜在的治疗靶点,但调节其细胞丰度和活性的机制,特别是其组成型表达和普遍存在的形式 ADAR1p110 的机制,仍知之甚少。在这里,我们报告 HECT 型 E3 泛素连接酶 SMURF2 是 ADAR1p110 的关键调节因子。我们表明,SMURF2 主要已知促进其蛋白质底物的泛素介导降解,可保护 ADAR1p110 免受蛋白水解,并促进其在人和鼠细胞和组织中的 A-to-I 编辑酶活性。在人细胞中进行的 ADAR1p110 相互作用组分析也表明 SMURF2 对 ADAR1p110 的稳定性和功能有积极影响。在机制上,我们发现 SMURF2 通过 ADAR1p110 赖氨酸-744(K744)的泛素化,以 E3 泛素连接酶依赖的方式直接结合、泛素化和稳定 ADAR1p110。该残基突变为精氨酸(K744R),这也与几种人类疾病有关,包括对称性色素失调症(DSH)和某些类型的癌症,消除了 SMURF2 介导的 ADAR1p110 免受蛋白酶体和溶酶体降解的保护,并使 ADAR1p110 介导的 RNA 编辑失活。我们的发现揭示了哺乳动物细胞中 ADAR1 调节的新机制,并表明 SMURF2 是影响 ADAR1p110 蛋白丰度、相互作用和功能的关键细胞因子。