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Genes (Basel). 2021 Jul 1;12(7):1026. doi: 10.3390/genes12071026.
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The role of RNA editing enzyme ADAR1 in human disease.ADAR1 酶在人类疾病中的作用。
Wiley Interdiscip Rev RNA. 2022 Jan;13(1):e1665. doi: 10.1002/wrna.1665. Epub 2021 Jun 8.
3
SMURF2-mediated ubiquitin signaling plays an essential role in the regulation of PARP1 PARylating activity, molecular interactions, and functions in mammalian cells.SMURF2 介导的泛素信号在调节 PARP1 的 PAR 酰化活性、分子相互作用以及在哺乳动物细胞中的功能方面发挥着重要作用。
FASEB J. 2021 Apr;35(4):e21436. doi: 10.1096/fj.202001759R.
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Decoupling expression and editing preferences of ADAR1 p150 and p110 isoforms.解耦 ADAR1 p150 和 p110 异构体的表达和编辑偏好。
Proc Natl Acad Sci U S A. 2021 Mar 23;118(12). doi: 10.1073/pnas.2021757118.
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ADAR1 RNA editing enzyme regulates R-loop formation and genome stability at telomeres in cancer cells.ADAR1 RNA 编辑酶调节癌细胞中端粒处 R 环的形成和基因组稳定性。
Nat Commun. 2021 Mar 12;12(1):1654. doi: 10.1038/s41467-021-21921-x.
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ADAR1 is a new target of METTL3 and plays a pro-oncogenic role in glioblastoma by an editing-independent mechanism.ADAR1 是 METTL3 的一个新靶点,通过一种非编辑依赖性机制在胶质母细胞瘤中发挥致癌作用。
Genome Biol. 2021 Jan 28;22(1):51. doi: 10.1186/s13059-021-02271-9.
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Evaluating the therapeutic potential of ADAR1 inhibition for triple-negative breast cancer.评估 ADAR1 抑制在三阴性乳腺癌中的治疗潜力。
Oncogene. 2021 Jan;40(1):189-202. doi: 10.1038/s41388-020-01515-5. Epub 2020 Oct 27.
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Processing of small RNAs by DICER/ADAR1 complexes and their RNAi targets.DICER/ADAR1 复合物对小 RNA 的加工及其 RNAi 靶标。
RNA. 2020 Dec;26(12):1801-1814. doi: 10.1261/rna.076745.120. Epub 2020 Aug 17.
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Unbiased Identification of trans Regulators of ADAR and A-to-I RNA Editing.无偏鉴定 ADAR 和 A-to-I RNA 编辑的反式调控因子。
Cell Rep. 2020 May 19;31(7):107656. doi: 10.1016/j.celrep.2020.107656.
10
Ubiquitination-mediated degradation of SIRT1 by SMURF2 suppresses CRC cell proliferation and tumorigenesis.SMURF2 通过泛素化介导的 SIRT1 降解抑制 CRC 细胞增殖和肿瘤发生。
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E3 泛素连接酶 SMURF2 稳定 RNA 编辑酶 ADAR1p110,并促进其腺嘌呤到次黄嘌呤(A-to-I)编辑功能。

The E3 ubiquitin ligase SMURF2 stabilizes RNA editase ADAR1p110 and promotes its adenosine-to-inosine (A-to-I) editing function.

机构信息

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.

出版信息

Cell Mol Life Sci. 2022 Apr 11;79(5):237. doi: 10.1007/s00018-022-04272-8.

DOI:10.1007/s00018-022-04272-8
PMID:35403872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11072456/
Abstract

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.

摘要

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。