Thakur S, Dhiman M, Tell G, Mantha A K
Center for Biosciences, School of Basic and Applied Sciences, Central University of Punjab, Bathinda, Punjab, India.
Cell Biochem Funct. 2015 Apr;33(3):101-12. doi: 10.1002/cbf.3100. Epub 2015 Mar 19.
Apurinic/apyrimidinic endonuclease 1 (APE1) is a classic example of functionally variable protein. Besides its well-known role in (i) DNA repair of oxidative base damage, APE1 also plays a critical role in (ii) redox regulation of transcription factors controlling gene expression for cell survival pathways, for which it is also known as redox effector factor 1 (Ref-1), and recent evidences advocates for (iii) coordinated control of other non-canonical protein-protein interaction(s) responsible for significant biological functions in mammalian cells. The diverse functions of APE1 can be ascribed to its ability to interact with different protein partners, owing to the attainment of unfolded domains during evolution. Association of dysregulation of APE1 with various human pathologies, such as cancer, cardiovascular diseases and neurodegeneration, is attributable to its multifunctional nature, and this makes APE1 a potential therapeutic target. This review covers the important aspects of APE1 in terms of its significant protein-protein interaction(s), and this knowledge is required to understand the onset and development of human pathologies and to design or improve the strategies to target such interactions for treatment and management of various human diseases.
脱嘌呤/脱嘧啶内切酶1(APE1)是功能可变蛋白的一个经典例子。除了其在(i)氧化碱基损伤的DNA修复中众所周知的作用外,APE1在(ii)控制细胞存活途径基因表达的转录因子的氧化还原调节中也起着关键作用,为此它也被称为氧化还原效应因子1(Ref-1),并且最近的证据支持(iii)对负责哺乳动物细胞中重要生物学功能的其他非经典蛋白质-蛋白质相互作用的协调控制。APE1的多种功能可归因于其与不同蛋白质伙伴相互作用的能力,这是由于在进化过程中获得了未折叠结构域。APE1失调与各种人类疾病如癌症、心血管疾病和神经退行性疾病的关联归因于其多功能性质,这使得APE1成为一个潜在的治疗靶点。本综述涵盖了APE1在其重要蛋白质-蛋白质相互作用方面的重要内容,而这些知识对于理解人类疾病的发生和发展以及设计或改进针对此类相互作用的策略以治疗和管理各种人类疾病是必需的。