Department of Microbiology, College of Medicine, Gachon University, Incheon, Korea.
Department of Health Science and Technology, GAIHST, Gachon University, Incheon, Korea.
Exp Mol Med. 2019 Jan 7;51(1):1-10. doi: 10.1038/s12276-018-0196-9.
Tryptophanyl tRNA synthetase (WRS) is an essential enzyme as it catalyzes the ligation of tryptophan to its cognate tRNA during translation. Interestingly, mammalian WRS has evolved to acquire domains or motifs for novel functions beyond protein synthesis; WRS can also further expand its functions via alternative splicing and proteolytic cleavage. WRS is localized not only to the nucleus but also to the extracellular space, playing a key role in innate immunity, angiogenesis, and IFN-γ signaling. In addition, the expression of WRS varies significantly in different tissues and pathological states, implying that it plays unique roles in physiological homeostasis and immune defense. This review addresses the current knowledge regarding the evolution, structural features, and context-dependent functions of WRS, particularly focusing on its roles in immune regulation.
色氨酰 tRNA 合成酶 (WRS) 是一种必需的酶,因为它在翻译过程中催化色氨酸与其对应的 tRNA 的连接。有趣的是,哺乳动物 WRS 已经进化出具有新功能的结构域或基序,超越了蛋白质合成;WRS 还可以通过选择性剪接和蛋白水解切割进一步扩展其功能。WRS 不仅定位于细胞核,还定位于细胞外空间,在先天免疫、血管生成和 IFN-γ 信号转导中发挥关键作用。此外,WRS 在不同组织和病理状态下的表达差异很大,这表明它在生理稳态和免疫防御中发挥着独特的作用。本文综述了 WRS 的进化、结构特征和上下文相关功能的最新知识,特别关注其在免疫调节中的作用。