Munn A L, Riezman H
Department of Biochemistry, Biozentrum of the University of Basel, Switzerland.
J Cell Biol. 1994 Oct;127(2):373-86. doi: 10.1083/jcb.127.2.373.
Yeast mutants that are defective in acidification of the lysosome-like vacuole are able to grow at pH 5.5, but not at pH 7. Here, we present evidence that endocytosis is required for this low pH-dependent growth and use this observation to develop a screen for mutants defective in endocytosis. By isolating mutants that cannot grow when they lack the 60-kD vacuolar ATPase subunit (encoded by the VAT2 gene), we isolated a number of vat2-synthetic lethal (Vsl-) mutant strains. Seven of the Vsl- mutants are defective in endocytosis. Four of these mutant strains (end8-1, end9-1, end10-1, and end11-1) show altered uptake of the endocytosed ligand, alpha-factor, and three (end12-1, end12-2, and end13-1) are probably defective in transfer of internalized material to the vacuole. Most of the mutations also confer a strong Ts- growth defect. The mutants defective in uptake of alpha-factor sort newly synthesized vacuolar proteins correctly, while those which may be defective in subsequent transport steps secrete at least a fraction of the newly synthesized soluble vacuolar proteins. The mutations that result in a defect in alpha-factor uptake are not allelic to any of the genes previously shown to encode endocytic functions.
在溶酶体样液泡酸化方面存在缺陷的酵母突变体能够在pH 5.5下生长,但不能在pH 7下生长。在此,我们提供证据表明内吞作用是这种低pH依赖性生长所必需的,并利用这一观察结果开发了一种筛选内吞作用缺陷突变体的方法。通过分离那些在缺乏60-kD液泡ATP酶亚基(由VAT2基因编码)时无法生长的突变体,我们分离出了许多vat2合成致死(Vsl-)突变株。其中七个Vsl-突变体在内吞作用方面存在缺陷。这些突变株中的四个(end8-1、end9-1、end10-1和end11-1)显示出内吞配体α-因子的摄取发生改变,另外三个(end12-1、end12-2和end13-1)可能在将内化物质转运至液泡方面存在缺陷。大多数突变还导致强烈的温度敏感(Ts-)生长缺陷。在摄取α-因子方面存在缺陷的突变体能够正确分选新合成的液泡蛋白,而那些可能在后续转运步骤中存在缺陷的突变体则至少分泌一部分新合成的可溶性液泡蛋白。导致α-因子摄取缺陷的突变与先前显示编码内吞功能的任何基因均无等位关系。