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KRE5 Suppression Induces Cell Wall Stress and Alternative ER Stress Response Required for Maintaining Cell Wall Integrity in Candida glabrata

机译:KRE5抑制诱导了光滑念珠菌的细胞壁应力和维持细胞壁完整性所需的替代性ER应力反应

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摘要

The maintenance of cell wall integrity in fungi is required for normal cell growth, division, hyphae formation, and antifungal tolerance. We observed that endoplasmic reticulum stress regulated cell wall integrity in Candida glabrata, which possesses uniquely evolved mechanisms for unfolded protein response mechanisms. Tetracycline-mediated suppression of KRE5, which encodes a predicted UDP-glucose:glycoprotein glucosyltransferase localized in the endoplasmic reticulum, significantly increased cell wall chitin content and decreased cell wall β-1,6-glucan content. KRE5 repression induced endoplasmic reticulum stress-related gene expression and MAP kinase pathway activation, including Slt2p and Hog1p phosphorylation, through the cell wall integrity signaling pathway. Moreover, the calcineurin pathway negatively regulated cell wall integrity, but not the reduction of β-1,6-glucan content. These results indicate that KRE5 is required for maintaining both endoplasmic reticulum homeostasis and cell wall integrity, and that the calcineurin pathway acts as a regulator of chitin-glucan balance in the cell wall and as an alternative mediator of endoplasmic reticulum stress in C. glabrata.
机译:正常细胞生长,分裂,菌丝形成和抗真菌耐受性要求维持真菌细胞壁的完整性。我们观察到内质网应激调节了光滑念珠菌的细胞壁完整性,它具有展开的蛋白质反应机制的独特进化机制。四环素介导的KRE5抑制作用,其编码位于内质网的UDP-葡萄糖:糖蛋白葡糖基转移酶的预测序列,可显着增加细胞壁几丁质含量,并降低细胞壁β-1,6-葡聚糖含量。 KRE5抑制通过细胞壁完整性信号传导途径诱导内质网应激相关基因表达和MAP激酶途径活化,包括Slt2p和Hog1p磷酸化。此外,钙调神经磷酸酶途径负调节细胞壁完整性,但不能降低β-1,6-葡聚糖含量。这些结果表明,KRE5是维持内质网稳态和细胞壁完整性所必需的,而钙调神经磷酸酶途径可作为细胞壁中几丁质-葡聚糖平衡的调节剂,并作为光滑小球藻内质网应激的替代介质。

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