Department of Biochemistry and Molecular Biology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205, USA.
Cells. 2023 Dec 20;13(1):8. doi: 10.3390/cells13010008.
Small ubiquitin-related modifiers (SUMOs) function as post-translational protein modifications and regulate nearly every aspect of cellular function. While a single ubiquitin protein is expressed across eukaryotic organisms, multiple SUMO paralogues with distinct biomolecular properties have been identified in plants and vertebrates. Five SUMO paralogues have been characterized in humans, with SUMO1, SUMO2 and SUMO3 being the best studied. SUMO2 and SUMO3 share 97% protein sequence homology (and are thus referred to as SUMO2/3) but only 47% homology with SUMO1. To date, thousands of putative sumoylation substrates have been identified thanks to advanced proteomic techniques, but the identification of SUMO1- and SUMO2/3-specific modifications and their unique functions in physiology and pathology are not well understood. The SUMO2/3 paralogues play an important role in proteostasis, converging with ubiquitylation to mediate protein degradation. This function is achieved primarily through SUMO-targeted ubiquitin ligases (STUbLs), which preferentially bind and ubiquitylate poly-SUMO2/3 modified proteins. Effects of the SUMO1 paralogue on protein solubility and aggregation independent of STUbLs and proteasomal degradation have also been reported. Consistent with these functions, sumoylation is implicated in multiple human diseases associated with disturbed proteostasis, and a broad range of pathogenic proteins have been identified as SUMO1 and SUMO2/3 substrates. A better understanding of paralogue-specific functions of SUMO1 and SUMO2/3 in cellular protein quality control may therefore provide novel insights into disease pathogenesis and therapeutic innovation. This review summarizes current understandings of the roles of sumoylation in protein quality control and associated diseases, with a focus on the specific effects of SUMO1 and SUMO2/3 paralogues.
小泛素相关修饰物(SUMOs)作为翻译后蛋白质修饰物发挥作用,调节细胞功能的几乎各个方面。虽然在真核生物中表达了单个泛素蛋白,但在植物和脊椎动物中已鉴定出具有不同生物分子特性的多个 SUMO 同源物。在人类中已鉴定出 5 种 SUMO 同源物,其中 SUMO1、SUMO2 和 SUMO3 研究得最为透彻。SUMO2 和 SUMO3 的蛋白质序列同源性高达 97%(因此称为 SUMO2/3),但与 SUMO1 的同源性仅为 47%。迄今为止,由于先进的蛋白质组学技术,已经鉴定出数千种假定的 SUMO 化底物,但 SUMO1 和 SUMO2/3 特异性修饰的鉴定及其在生理学和病理学中的独特功能尚未得到很好的理解。SUMO2/3 同源物在蛋白质稳态中发挥着重要作用,与泛素化协同作用来介导蛋白质降解。这一功能主要是通过 SUMO 靶向泛素连接酶(STUbLs)实现的,后者优先结合并泛素化多 SUMO2/3 修饰的蛋白质。SUMO1 同源物对 STUbLs 和蛋白酶体降解以外的蛋白质可溶性和聚集的影响也有报道。与这些功能一致,SUMO 化与多种与蛋白质稳态失调相关的人类疾病有关,并且已鉴定出广泛的致病性蛋白质作为 SUMO1 和 SUMO2/3 的底物。因此,对 SUMO1 和 SUMO2/3 同源物在细胞蛋白质质量控制中的特定功能的更好理解可能为疾病发病机制和治疗创新提供新的见解。本综述总结了 SUMO 化在蛋白质质量控制和相关疾病中的作用的现有认识,重点介绍了 SUMO1 和 SUMO2/3 同源物的特定作用。