Dilcher Meik, Veith Beate, Chidambaram Subbulakshmi, Hartmann Enno, Schmitt Hans Dieter, Fischer von Mollard Gabriele
Abteilung Biochemie II, Universität Göttingen, Heinrich-Düker Weg 12, D-37073 Göttingen, Germany.
EMBO J. 2003 Jul 15;22(14):3664-74. doi: 10.1093/emboj/cdg339.
SNAREs on transport vesicles and target membranes are required for vesicle targeting and fusion. Here we describe a novel yeast protein with a typical SNARE motif but with low overall amino acid homologies to other SNAREs. The protein localized to the endoplasmic reticulum (ER) and was therefore named Use1p (unconventional SNARE in the ER). A temperature-sensitive use1 mutant was generated. use1 mutant cells accumulated the ER forms of carboxypeptidase Y and invertase. More specific assays revealed that use1 mutant cells were defective in retrograde traffic to the ER. This was supported by strong genetic interactions between USE1 and the genes encoding SNAREs in retrograde traffic to the ER. Antibodies directed against Use1p co-immunoprecipitated the SNAREs Ufe1p, myc-Sec20p and Sec22p, which form a SNARE complex required for retrograde traffic from the Golgi to the ER, but neither Bos1p nor Bet1p (members of the SNARE complex in anterograde traffic to the Golgi). Therefore, we conclude that Use1p is a novel SNARE protein that functions in retrograde traffic from the Golgi to the ER.
转运囊泡和靶膜上的SNARE蛋白对于囊泡的靶向和融合是必需的。在此,我们描述了一种新型酵母蛋白,它具有典型的SNARE基序,但与其他SNARE蛋白的整体氨基酸同源性较低。该蛋白定位于内质网(ER),因此被命名为Use1p(内质网中的非常规SNARE蛋白)。构建了一个温度敏感型use1突变体。use1突变体细胞积累了羧肽酶Y和转化酶的内质网形式。更具体的分析表明,use1突变体细胞在内质网逆行运输中存在缺陷。这得到了USE1与内质网逆行运输中编码SNARE蛋白的基因之间强烈遗传相互作用的支持。针对Use1p的抗体共免疫沉淀了SNARE蛋白Ufe1p、myc-Sec20p和Sec22p,它们形成了从高尔基体到内质网逆行运输所需的SNARE复合体,但没有沉淀Bos1p和Bet1p(顺行运输到高尔基体的SNARE复合体成员)。因此,我们得出结论,Use1p是一种新型SNARE蛋白,在从高尔基体到内质网的逆行运输中发挥作用。