PROTEIN SORTING TO THE LYSOSOME-LIKE VACUOLE IN YEAST

黄曲霉毒素的选择性识别、分选和囊泡介导的转运 通过分泌途径的蛋白质代表了 所有真核细胞。精确的机械装置和机械装置 这些过程尚不清楚。我们已经分离出一大批 在蛋白质输送过程中表现出严重和特定缺陷的酵母突变株 酵母菌中的溶酶体样液泡。其中有缺陷的基因 突变体很可能编码细胞蛋白质分类的组成部分 仪器。走向对分子和生化基础的理解 对于这些突变体(VP)中的空泡蛋白分选缺陷，我们提出了 确定某些VPS基因及其产物所起的作用 在将液泡酶从高尔基复合体分选和运送到 液泡。酵母与其他酵母的基本相似之处 真核细胞在其蛋白质传递途径中，连同 酵母中强大的遗传和分子方法，使酵母成为 是解决这些问题的理想有机体。它在医学上的重要性 这种分选途径以严重的溶酶体存储为例 疾病(如i-细胞病、假性赫勒氏多发性营养不良以及其他 疾病(例如骨质疏松症和某些类型癌症的进展) 这是由溶酶体的错误定位引起的或与之相关的 水解酶。 实验室已经克隆了8个VPS基因并进行了测序。要确定 这些基因的产物在哪里以及如何作用于指导分类和 液泡水解酶的传递，我们建议：1)使用间接 免疫荧光和细胞分级技术测定 VPS基因产物的亚细胞定位，2)分离温度- 条件VPs等位基因分析空泡起始动力学 蛋白质分选缺陷并确定潜在的中间体 分选过程，3)采用基因抑制和化学交联法 用于鉴定和表征VPS基因产物之间相互作用的试剂， 4)使用重组空泡蛋白递送的体外试验来 描述VPS蛋白的阶段特异性需求和功能， 和5)克隆和测序某些VPS基因的功能同源物 裂殖酵母和哺乳动物(人)的cDNA文库 细胞类型开始分析VPS基因产物的功能作用 在其他真核生物中发挥作用。预计这些研究将导致 在蛋白质分选和控制的组织和控制的详细视图中 高尔基体与液泡/溶酶体之间的囊泡运输 酵母和其他真核生物。

The selective recognition, sorting and vesicle-mediated transport of proteins through the secretory pathway represents an essential feature of all eukaryotic cells. The precise mechanisms and machinery that direct these processes are not yet known. We have isolated a large collection of yeast mutants that exhibit severe and specific defects in protein delivery to the lysosome-like vacuole in yeast. The defective genes in these mutants are likely to encode components of the cells' protein sorting apparatus. Toward an understanding of the molecular and biochemical basis of the vacuolar protein sorting defects in these mutants (vps), we propose to characterize the roles certain of the VPS genes and their products play in the sorting and delivery of vacuolar enzymes from the Golgi complex to the vacuole. The fundamental similarities between yeast and other eukaryotic cells in their pathways for protein delivery, together with the powerful genetic and molecular approaches available in yeast, make yeast an ideal organism for addressing these problems. The medical importance of this sorting pathway is exemplified by the serious lysosomal storage diseases (e.g. I-cell disease, pseudo-Hurler polydystrophy as well as other diseases (e.g. osteoporosis and the progression of certain types of cancer) that result from, or are correlated with, mislocalization of lysosomal hydrolases. Eight VPS genes have been cloned and sequenced in the lab. To determine where and how the products of these genes act to direct the sorting and delivery of vacuolar hydrolases, we propose to: 1) use indirect immunofluorescence and cell fractionation techniques to determine the subcellular location of the VPS gene products, 2) isolate temperature- conditional vps alleles to analyze the onset kinetics of the vacuolar protein sorting defects and to identify potential intermediates in the sorting process, 3) use genetic suppression and chemical cross-linking agents to identify and characterize interactions among VPS gene products, 4) employ an in vitro assay that reconstitutes vacuolar protein delivery to characterize the stage specific requirements and functions of Vps proteins, and 5) clone and sequence functional homologs for certain VPS genes from cDNA libraries of Schizosaccharomyces pombe as well as mammalian (human) cell types to begin an analysis of the functional role VPS gene products play in other eukaryotes. It is anticipated that these studies will result in a detailed view of the organization and control of protein sorting and vesicular traffic between the Golgi complex and the vacuole/lysosome in yeast and other eukaryotes.