State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200240, P.R. China.
J Cell Sci. 2021 Jun 1;134(11). doi: 10.1242/jcs.257337. Epub 2021 Jun 4.
The classical neurotransmitter serotonin or 5-hydroxytryptamine (5-HT), synthesized from tryptophan, can be produced both centrally and peripherally. Through binding to functionally distinct receptors, serotonin is profoundly implicated in a number of fundamental physiological processes and pathogenic conditions. Recently, serotonin has been found covalently incorporated into proteins, a newly identified post-translational modification termed serotonylation. Transglutaminases (TGMs), especially TGM2, are responsible for catalyzing the transamidation reaction by transferring serotonin to the glutamine residues of target proteins. Small GTPases, extracellular matrix protein fibronectin, cytoskeletal proteins and histones are the most reported substrates for serotonylation, and their functions are triggered by this post-translational modification. This Review highlights the roles of serotonylation in physiology and diseases and provides perspectives for pharmacological interventions to ameliorate serotonylation for disease treatment.
经典神经递质血清素或 5-羟色胺(5-HT)由色氨酸合成,可以在中枢和外周产生。通过与功能不同的受体结合,血清素深刻地参与了许多基本的生理过程和致病条件。最近,人们发现血清素被共价整合到蛋白质中,这是一种新发现的翻译后修饰,称为血清素化。转谷氨酰胺酶(TGMs),特别是 TGM2,负责通过将血清素转移到靶蛋白的谷氨酰胺残基上来催化转酰胺反应。小 GTP 酶、细胞外基质蛋白纤维连接蛋白、细胞骨架蛋白和组蛋白是报道最多的血清素化底物,其功能由这种翻译后修饰触发。本综述强调了血清素化在生理和疾病中的作用,并为通过改善血清素化来治疗疾病的药理学干预提供了新视角。