Department of Biology, McGill University, H3A 1B1, Quebec, Montreal, Canada.
Curr Genet. 1983 Nov;7(6):449-56. doi: 10.1007/BF00377610.
Two chromosomal mutations in yeast that result in oversecretion of the K1 killer toxin protein were examined. A recessive mutation in gene ski5 appears to lead to toxin oversecretion through a defect in a cell surface, PMSF-inhibited protease. A wild type killer strain degraded toxin following synthesis, and degradation could be partially prevented by addition of PMSF to the growth medium. The ski5 mutation caused an approximate ten fold oversecretion of toxin, similar to that seen in a PMSF-treated wild type culture, and no increased oversecretion in the presence of PMSF. The ski5 mutation caused oversecretion of other low molecular weight secreted proteins and appeared to oversecrete the α-factor pheromone, as judged by activity tests. The ski5 mutation was complemented by mutations in ski genes 1-4, and the mutant was not supersensitive to mating pheromones or K2 killer toxin.We also examined killer strains with a mutation in the nuclear gene krel which results in a defective (1→6)-β-D-glucan cell wall receptor for killer toxin. Such strains oversecrete toxin into the growth medium, but also, unexpectedly, oversecrete most other secreted proteins. The defect in (1→6)-β-D-glucan in these mutants appears to perturb the partitioning of secreted proteins between the cell wall and the medium.
研究了导致酵母中 K1 杀伤毒素蛋白过度分泌的两种染色体突变。基因 ski5 的隐性突变似乎通过细胞表面 PMSF 抑制的蛋白酶缺陷导致毒素过度分泌。野生型杀伤菌株在合成后降解毒素,并且在生长培养基中添加 PMSF 可以部分阻止降解。ski5 突变导致毒素过度分泌约 10 倍,类似于 PMSF 处理的野生型培养物中观察到的情况,并且在 PMSF 存在下没有增加过度分泌。ski5 突变导致其他低分子量分泌蛋白的过度分泌,并且似乎分泌了 α 因子信息素,这可以通过活性测试来判断。ski5 突变可以被 ski 基因 1-4 的突变所补偿,并且突变体对交配信息素或 K2 杀伤毒素不敏感。我们还研究了核基因 krel 突变的杀伤菌株,该突变导致杀伤毒素的缺陷(1→6)-β-D-葡聚糖细胞壁受体。这种菌株将毒素过度分泌到生长培养基中,但出乎意料的是,也过度分泌了大多数其他分泌蛋白。这些突变体中(1→6)-β-D-葡聚糖的缺陷似乎扰乱了分泌蛋白在细胞壁和培养基之间的分配。