Uehata Takuya, Takeuchi Osamu
1 Laboratory of Infection and Prevention, Institute for Frontier Life and Medical Sciences, Kyoto University , Kyoto, Japan .
2 CREST , AMED-CREST, Kyoto, Japan .
J Interferon Cytokine Res. 2017 May;37(5):220-229. doi: 10.1089/jir.2017.0001.
Regnase-1, also known as Zc3h12a or MCPIP1, is responsible for endonucleolytic cleavage of mRNAs encoding proteins involved in inflammatory responses. Furthermore, Regnase-1-mediated mRNA decay (RMD) is critical for the maintenance of immune homeostasis. Regnase-1 controls the magnitude of innate and adaptive immune responses, and thereby dysfunction of this protein in mice leads to the development of spontaneous systemic inflammation. During the last several years, advances have been made in understanding molecular mechanisms of RMD. In this article, unique functions of Regnase-1 in controlling inflammation are discussed.
核糖核酸酶1(Regnase-1),也被称为锌指CCCH型包含12A(Zc3h12a)或单核细胞趋化蛋白诱导蛋白1(MCPIP1),负责对编码参与炎症反应的蛋白质的信使核糖核酸(mRNA)进行核酸内切酶切割。此外,核糖核酸酶1介导的信使核糖核酸衰变(RMD)对于维持免疫稳态至关重要。核糖核酸酶1控制先天性和适应性免疫反应的强度,因此该蛋白在小鼠中的功能失调会导致自发性全身炎症的发展。在过去几年中,在理解核糖核酸酶1介导的信使核糖核酸衰变的分子机制方面取得了进展。本文将讨论核糖核酸酶1在控制炎症方面的独特功能。