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首页> 外文期刊>FEMS Yeast Research >Phosphatidylinositol 3-kinase VPS34 of Candida albicans is involved in filamentous growth, secretion of aspartic proteases, and intracellular detoxification
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Phosphatidylinositol 3-kinase VPS34 of Candida albicans is involved in filamentous growth, secretion of aspartic proteases, and intracellular detoxification

机译:白色念珠菌的磷脂酰肌醇3-激酶VPS34参与丝状生长,天冬氨酸蛋白酶的分泌和细胞内排毒

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摘要

The phosphatidylinositol (PI) 3-kinase Vps34p of Candida albicans influences vesicular intracellular transport, filamentous growth and virulence. To get a clearer understanding how these phenomena are connected, we analysed hyphal growth in a matrix under microaerophilic conditions at low temperature, the detoxification of metal ions and antifungal drugs, the secretion of aspartic proteinases (Saps), as well as expression of adhesion-associated proteins of the C. albicans vps34 null mutant strain. The hyphal growth in a matrix, which is repressed in the wild-type strain by Efg1p, was derepressed in the mutant. CZF1, which encodes an activator of hyphal growth in a matrix, was up-regulated in the mutant. In addition, CZF1 expression was pH-dependent in the wild-type. Expression of EFG1 was not changed. Examination of Saps secretion showed a reduction in the vps34 null mutant. Determination of sensitivity against metal ions and antimycotic drugs revealed defects in detoxification. Expression studies indicated that the vps34 mutant reacts to the phenotypical defects with an up-regulation of genes involved in these processes, including the aspartyl proteinases SAP2 and SAP9, adhesion proteins ALS1 and HWP1, and the ABC transporters CDR1 and HST6. We also found an increased expression of the PI 4-kinase LSB6 indicating a complex feed-back mechanism for the compensation of the multiple defects arising from the lack of the PI3-kinase VPS34.
机译:白色念珠菌的磷脂酰肌醇(PI)3-激酶Vps34p影响囊泡的细胞内转运,丝状生长和毒力。为了更清楚地了解这些现象之间的联系,我们分析了在低温微需氧条件下基质中的菌丝生长,金属离子和抗真菌药物的解毒作用,天冬氨酸蛋白酶(Saps)的分泌以及黏附的表达-白念珠菌vps34空突变株的相关蛋白。 Efg1p在野生型菌株中抑制的基质中菌丝的生长在突变体中被抑制。 CZF1,在基质中编码菌丝生长的激活剂,在突变体中被上调。另外,在野生型中CZF1表达是pH依赖性的。 EFG1的表达未改变。对Saps分泌物的检查表明vps34无效突变体的减少。对金属离子和抗真菌药物的敏感性测定表明,排毒存在缺陷。表达研究表明,vps34突变体对表型缺陷有反应,这些基因参与了这些过程的上调,包括天冬氨酰蛋白酶SAP2和SAP9,粘附蛋白ALS1和HWP1以及ABC转运蛋白CDR1和HST6。我们还发现PI 4激酶LSB6的表达增加,表明有一种复杂的反馈机制可以补偿由于缺少PI3激酶VPS34而引起的多种缺陷。

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