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首页> 外文期刊>Applied and Environmental Microbiology >Characterization of Secretory Genes ypt1/yptA and nsf1sfA from Two Filamentous Fungi: Induction of Secretory Pathway Genes of Trichoderma reesei under Secretion Stress Conditions
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Characterization of Secretory Genes ypt1/yptA and nsf1sfA from Two Filamentous Fungi: Induction of Secretory Pathway Genes of Trichoderma reesei under Secretion Stress Conditions

机译:两种丝状真菌分泌基因ypt1 / yptA和nsf1 / nsfA的表征:分泌应激条件下里氏木霉分泌途径基因的诱导

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Two genes involved in protein secretion, encoding the Rab protein YPT1/YPTA and the general fusion factor NSFI/NSFA, were characterized from two filamentous fungi, Trichoderma reesei and Aspergillus niger var. awamori. The isolated genes showed a high level of conservation with their Saccharomyces cerevisiae and mammalian counterparts, and T. reesei ypt1 was shown to complement yeast Ypt1p depletion. The transcriptional regulation of the T. reesei ypt1, nsf1, and sar1 genes, involved in protein trafficking, was studied with mycelia treated with the folding inhibitor dithiothreitol (DTT) and with brefeldin A, which inhibits membrane traffic between the endoplasmic reticulum and Golgi complex. The well-known inducer of the yeast and T. reesei unfolded protein response (UPR), DTT, induced the nsf1 gene and the protein disulfide isomerase gene, pdi1, in both of the experiments, and sar1 mRNA increased in only one experiment under strong UPR induction. The ypt1 mRNA did not show a clear increase during DTT treatment. Brefeldin A strongly induced pdi1 and all of the intracellular trafficking genes studied. These results suggest the possibility that the whole secretory pathway of T. reesei could be induced at the transcriptional level by stress responses caused by protein accumulation in the secretory pathway.
机译:从两个丝状真菌里氏木霉和黑曲霉中鉴定了两个涉及蛋白质分泌的基因,分别编码Rab蛋白YPT1 / YPTA和一般融合因子NSFI / NSFA。泡盛分离出的基因与酿酒酵母和哺乳动物对应基因表现出高度的保守性,里氏木霉ypt1可以补充酵母Ypt1p的消耗。用折叠抑制剂二硫苏糖醇(DTT)和布雷菲德菌素A处理的菌丝体研究了参与蛋白质运输的里氏木霉ypt1,nsf1和sar1基因的转录调控,其抑制了内质网和高尔基体之间的膜运输。 。酵母和里氏木霉的众所周知的诱导物未折叠蛋白反应(UPR)DTT在两个实验中均诱导了nsf1基因和蛋白二硫键异构酶基因pdi1,而在一个实验中,在强烈的条件下sar1 mRNA却增加了普遍定期审议。 ypt1 mRNA在DTT治疗期间未显示明显增加。布雷菲德菌素A强烈诱导pdi1和所有研究的细胞内运输基因。这些结果表明,通过分泌途径中蛋白质积累引起的应激反应,可以在转录水平上诱导里氏木霉的整个分泌途径。

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