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不同的SEC基因集在分泌途径的早期控制运输小泡的形成和融合。

Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway.

作者信息

Kaiser C A, Schekman R

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley 94720.

出版信息

Cell. 1990 May 18;61(4):723-33. doi: 10.1016/0092-8674(90)90483-u.

Abstract

A vesicular intermediate in protein transport from the endoplasmic reticulum is detected in a subset of temperature-sensitive mutants blocked early in the yeast secretory pathway. By electron microscopy three of the mutants, sec18, sec17, and sec22, accumulate 50 nm vesicles at the nonpermissive temperature. Vesicle accumulation is blocked by the mutations sec12, sec13, sec16, and sec23 as shown by analysis of double-mutant strains. Thus the early SEC genes can be divided into vesicle forming and vesicle fusion functions. Synthetic lethal interactions between sec mutations define two groups of SEC genes, corresponding to the groups involved in vesicle formation or fusion. Mutations in two of the genes involved in vesicle fusion, SEC17 and SEC18, are lethal in combination, and five of six possible pairwise combinations of mutations in genes required for vesicle formation, SEC12, SEC13, SEC16, and SEC23, are lethal. These interactions suggest cooperation between different SEC gene products in vesicle budding and vesicle fusion processes.

摘要

在酵母分泌途径早期受阻的一组温度敏感突变体中,检测到一种在内质网蛋白质运输过程中的囊泡中间体。通过电子显微镜观察,其中三个突变体sec18、sec17和sec22在非允许温度下积累50纳米的囊泡。如对双突变菌株的分析所示,sec12、sec13、sec16和sec23突变会阻止囊泡的积累。因此,早期的SEC基因可分为囊泡形成和囊泡融合功能两类。sec突变之间的合成致死相互作用定义了两组SEC基因,分别对应参与囊泡形成或融合的组。参与囊泡融合的两个基因SEC17和SEC18中的突变组合是致死的,而参与囊泡形成所需的基因SEC12、SEC13、SEC16和SEC23中六种可能的两两突变组合中有五种是致死的。这些相互作用表明不同的SEC基因产物在囊泡出芽和囊泡融合过程中存在合作。

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