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综述:IRE1 的两面性及其在植物抵御胁迫中的作用。

Review: The two faces of IRE1 and their role in protecting plants from stress.

机构信息

Plant Sciences Institute, Iowa State University, Ames, Iowa, USA.

Plant Sciences Institute, Iowa State University, Ames, Iowa, USA.

出版信息

Plant Sci. 2021 Feb;303:110758. doi: 10.1016/j.plantsci.2020.110758. Epub 2020 Nov 18.

Abstract

IRE1 is a key factor in the Unfolded Protein Response (UPR) in plants. IRE1 is a single-pass transmembrane protein that has a lumenal domain (LD) and cytoplasmic domain (CD), which perform quite different tasks on different sides of the ER membrane. The LD recognizes the presence of misfolded proteins in the ER lumen. The LDs of IRE1 in different plant species are predicted to fold into β-propeller structures with surfaces for protein-protein interactions. Likewise, the CDs of plant IRE1s have predicted structural interfaces that promote the face-to-face arrangements of IRE1 for transphosphorylation and back-to-back arrangements for RNA splicing. Hence, the structures on the different faces of plant IRE1s have unique features for recognizing problems of protein folding in the ER and transducing that signal to activate the UPR.

摘要

IRE1 是植物未折叠蛋白反应 (UPR) 的关键因素。IRE1 是一种单次跨膜蛋白,具有内质网腔域 (LD) 和细胞质域 (CD),它们在 ER 膜的两侧执行非常不同的任务。LD 识别 ER 腔中错误折叠的蛋白质的存在。不同植物物种的 IRE1 的 LD 预计会折叠成具有用于蛋白质-蛋白质相互作用的表面的 β-桨叶结构。同样,植物 IRE1 的 CDs 具有预测的结构界面,促进 IRE1 的面对面排列以进行磷酸转移,以及背对背排列以进行 RNA 剪接。因此,植物 IRE1 不同面的结构具有独特的特征,可用于识别 ER 中蛋白质折叠的问题,并将该信号转导以激活 UPR。

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