Buschhorn Bettina A, Kostova Zlatka, Medicherla Balasubrahmanyam, Wolf Dieter H
Institut für Biochemie, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany.
FEBS Lett. 2004 Nov 19;577(3):422-6. doi: 10.1016/j.febslet.2004.10.039.
We undertook a growth-based screen exploiting the degradation of CTL*, a chimeric membrane-bound ERAD substrate derived from soluble lumenal CPY*. We screened the Saccharomyces cerevisiae genomic deletion library containing approximately 5000 viable strains for mutants defective in endoplasmic reticulum (ER) protein quality control and degradation (ERAD). Among the new gene products we identified Yos9p, an ER-localized protein previously involved in the processing of GPI anchored proteins. We show that deficiency in Yos9p affects the degradation only of glycosylated ERAD substrates. Degradation of non-glycosylated substrates is not affected in cells lacking Yos9p. We propose that Yos9p is a lectin or lectin-like protein involved in the quality control of N-glycosylated proteins. It may act sequentially or in concert with the ERAD lectin Htm1p/Mnl1p (EDEM) to prevent secretion of malfolded glycosylated proteins and deliver them to the cytosolic ubiquitin-proteasome machinery for elimination.
我们利用源自可溶性腔CPY的嵌合膜结合ERAD底物CTL的降解进行了基于生长的筛选。我们在包含约5000个存活菌株的酿酒酵母基因组缺失文库中筛选内质网(ER)蛋白质质量控制和降解(ERAD)缺陷的突变体。在我们鉴定出的新基因产物中,有Yos9p,一种先前参与GPI锚定蛋白加工的内质网定位蛋白。我们表明,Yos9p缺陷仅影响糖基化ERAD底物的降解。在缺乏Yos9p的细胞中,非糖基化底物的降解不受影响。我们提出Yos9p是一种凝集素或凝集素样蛋白,参与N-糖基化蛋白的质量控制。它可能与ERAD凝集素Htm1p/Mnl1p(EDEM)顺序作用或协同作用,以防止错误折叠的糖基化蛋白分泌,并将它们递送至胞质泛素-蛋白酶体机制进行清除。