Chen Y J, Stevens T H
Institute of Molecular Biology, University of Oregon, Eugene 97403-1229, USA.
Eur J Cell Biol. 1996 Aug;70(4):289-97.
To better understand the process of protein sorting to the yeast vacuole, the VPS8 gene was identified and characterized. VPS8 encodes a membrane-associated hydrophilic protein of 135 kDa (Vps8p), which is required for the accurate sorting of the vacuolar hydrolase, carboxypeptidase Y (CPY). vps8 mutant cells missort and secrete CPY as well as a second soluble vacuolar hydrolase, proteinase A. In vps8 mutants, several late-Golgi membrane proteins fail to be retained in the Golgi apparatus. The Golgi-localized CPY sorting receptor, Vps10p, is mislocalized to and aberrantly proteolyzed in the vacuole. Based on our findings, we propose that Vps8p is part of a protein complex that associates with Golgi and post-Golgi membranes and functions in the retrieval of Golgi membrane proteins from the prevacuolar compartment.
为了更好地理解蛋白质分选至酵母液泡的过程,VPS8基因被鉴定并进行了表征。VPS8编码一种135 kDa的膜相关亲水性蛋白(Vps8p),它是液泡水解酶羧肽酶Y(CPY)准确分选所必需的。vps8突变细胞会错误分选并分泌CPY以及第二种可溶性液泡水解酶蛋白酶A。在vps8突变体中,几种晚期高尔基体膜蛋白无法保留在高尔基体中。高尔基体定位的CPY分选受体Vps10p会错误定位到液泡并在其中异常被蛋白酶水解。基于我们的研究结果,我们提出Vps8p是一种蛋白质复合物的一部分,该复合物与高尔基体和高尔基体后膜相关,并在从前液泡区室回收高尔基体膜蛋白中发挥作用。