E3泛素连接酶TRIM2被鉴定为CYP11B2和醛固酮产生的新抑制因子。

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Cellular and Molecular Life Sciences Pub Date : 2024-12-27 DOI:10.1007/s00018-024-05545-0
Liang Chen, Xuan Hu, Gang Wang, Fang Yu, Zhe Dai, Xiaobin Jian, Yong Li, Wan Xiang, Zhe Meng
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引用次数: 0

摘要

醛固酮生成腺瘤(APA)是原发性醛固酮增多症(PA)的主要原因,这是一种以醛固酮分泌过多为特征的疾病。CYP11B2是醛固酮合成酶,在醛固酮生物合成和APA的发展中起关键作用。尽管其意义重大,但CYP11B2的编码调控机制,特别是其降解机制,仍然知之甚少。在这项研究中,我们试图通过对E3泛素连接酶进行siRNA筛选来发现CYP11B2稳定性的新调节因子。我们的研究结果发现TRIM2是CYP11B2的关键负调节因子,其过表达导致肾上腺肿瘤细胞中CYP11B2蛋白水平显著降低,同时醛固酮产生减少。在机制上,我们证明TRIM2通过其RBCC结构域与CYP11B2相互作用,促进k29 /48连接的多泛素化和CYP11B2的不稳定。进一步的研究结果显示,TRIM2在APA组织中表达下调,在正常肾上腺组织的肾小球带(ZG)和束状带(ZF)中表达差异。这些发现强调了TRIM2作为一种通过CYP11B2降解醛固酮合成的新型调节剂,为APA提供了潜在的治疗靶点。
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E3 ubiquitin ligase TRIM2 identified as a novel suppressor of CYP11B2 and aldosterone production.

Aldosterone-producing adenoma (APA) is a leading cause of primary aldosteronism (PA), a condition marked by excessive aldosterone secretion. CYP11B2, the aldosterone synthase, plays a critical role in aldosterone biosynthesis and the development of APA. Despite its significance, encoding regulatory mechanisms governing CYP11B2, particularly its degradation, remain poorly understood. In this study, we sought to uncover novel regulators of CYP11B2 stability by conducting a siRNA screen targeting E3 ubiquitin ligases. Our results identified TRIM2 as a key negative regulator of CYP11B2, where its overexpression led to a significant reduction in CYP11B2 protein levels and a concomitant decrease in aldosterone production in adrenal tumor cells. Mechanistically, we demonstrated that TRIM2 interacts with CYP11B2 via its RBCC domain, promoting K29/48-linked polyubiquitination and destabilization of CYP11B2. Further results revealed that TRIM2 is downregulated in APA tissues, showing differential expression between the zona glomerulosa (ZG) and zona fasciculata (ZF) of normal adrenal tissue. These findings highlight TRIM2 as a novel modulator of aldosterone synthesis through CYP11B2 degradation, offering a potential therapeutic target for APA.

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来源期刊
Cellular and Molecular Life Sciences
Cellular and Molecular Life Sciences 生物-生化与分子生物学
CiteScore
13.20
自引率
1.20%
发文量
546
审稿时长
1.0 months
期刊介绍: Journal Name: Cellular and Molecular Life Sciences (CMLS) Location: Basel, Switzerland Focus: Multidisciplinary journal Publishes research articles, reviews, multi-author reviews, and visions & reflections articles Coverage: Latest aspects of biological and biomedical research Areas include: Biochemistry and molecular biology Cell biology Molecular and cellular aspects of biomedicine Neuroscience Pharmacology Immunology Additional Features: Welcomes comments on any article published in CMLS Accepts suggestions for topics to be covered
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