Cox J S, Shamu C E, Walter P
Department of Biochemistry and Biophysics, University of California Medical School, San Francisco 94143-0448.
Cell. 1993 Jun 18;73(6):1197-206. doi: 10.1016/0092-8674(93)90648-a.
The transcription of genes encoding soluble proteins that reside in the endoplasmic reticulum (ER) is induced when unfolded proteins accumulate in the ER. Thus, an intracellular signal transduction pathway must exist that mediates communication between the ER lumen and the nucleus. We have identified a gene in S. cerevisiae, IRE1, that is required for this pathway: ire1- mutants cannot activate transcription of KAR2 and PDI1, which encode the ER resident proteins BiP and protein disulfide isomerase. Moreover, IRE1 is essential for cell viability under stress conditions that cause unfolded proteins to accumulate in the ER. IRE1 encodes a transmembrane serine/threonine kinase that we propose transmits the unfolded protein signal across the ER or inner nuclear membrane. IRE1 is also required for inositol prototrophy, suggesting that the induction of ER resident proteins is coupled to the biogenesis of new ER membrane.
当内质网(ER)中积累未折叠蛋白时,编码驻留在内质网的可溶性蛋白的基因转录被诱导。因此,必然存在一条细胞内信号转导途径,介导内质网腔与细胞核之间的通讯。我们在酿酒酵母中鉴定出一个基因IRE1,它是该途径所必需的:ire1-突变体无法激活KAR2和PDI1的转录,这两个基因分别编码内质网驻留蛋白BiP和蛋白二硫键异构酶。此外,在导致未折叠蛋白在内质网中积累的应激条件下,IRE1对细胞活力至关重要。IRE1编码一种跨膜丝氨酸/苏氨酸激酶,我们认为它能将未折叠蛋白信号传递过内质网或内核膜。IRE1对于肌醇原养型也是必需的,这表明内质网驻留蛋白的诱导与新内质网膜的生物合成相关。