Rossi G, Kolstad K, Stone S, Palluault F, Ferro-Novick S
Department of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Mol Biol Cell. 1995 Dec;6(12):1769-80. doi: 10.1091/mbc.6.12.1769.
Here we report the identification of BET3, a new member of a group of interacting genes whose products have been implicated in the targeting and fusion of endoplasmic reticulum (ER) to Golgi transport vesicles with their acceptor compartment. A temperature-sensitive mutant in bet3-1 was isolated in a synthetic lethal screen designed to identify new genes whose products may interact with BET1, a type II integral membrane protein that is required for ER to Golgi transport. At 37 degrees C, bet3-1 fails to transport invertase, alpha-factor, and carboxypeptidase Y from the ER to the Golgi complex. As a consequence, this mutant accumulates dilated ER and small vesicles. The SNARE complex, a docking/fusion complex, fails to form in this mutant. Furthermore, BET3 encodes an essential 22-kDa hydrophilic protein that is conserved in evolution, which is not a component of this complex. These findings support the hypothesis that Bet3p may act before the assembly of the SNARE complex.
在此,我们报告了BET3的鉴定,它是一组相互作用基因的新成员,其产物与内质网(ER)到高尔基体运输囊泡与其受体区室的靶向和融合有关。在一个合成致死筛选中分离出bet3 - 1温度敏感突变体,该筛选旨在鉴定其产物可能与BET1相互作用的新基因,BET1是一种ER到高尔基体运输所需的II型整合膜蛋白。在37摄氏度时,bet3 - 1无法将转化酶、α - 因子和羧肽酶Y从ER运输到高尔基体复合体。因此,该突变体积累了扩张的ER和小囊泡。对接/融合复合体SNARE复合体在该突变体中无法形成。此外,BET3编码一种在进化中保守的必需的22 kDa亲水性蛋白,它不是该复合体的组成部分。这些发现支持了Bet3p可能在SNARE复合体组装之前起作用的假说。