首页> 美国卫生研究院文献>The Journal of Biological Chemistry >First Step of Glycosylphosphatidylinositol (GPI) Biosynthesis Cross-talks with Ergosterol Biosynthesis and Ras Signaling in Candida albicans
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First Step of Glycosylphosphatidylinositol (GPI) Biosynthesis Cross-talks with Ergosterol Biosynthesis and Ras Signaling in Candida albicans

机译:糖基磷脂酰肌醇(GPI)生物合成的第一步与白色念珠菌中麦角固醇生物合成和Ras信号的相互作用

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摘要

Candida albicans is a leading cause of fungal infections worldwide. It has several glycosylphosphatidylinositol (GPI)-anchored virulence factors. Inhibiting GPI biosynthesis attenuates its virulence. Building on our previous work, we explore the interaction of GPI biosynthesis in C. albicans with ergosterol biosynthesis and hyphal morphogenesis. This study is also the first report of transcriptional co-regulation existing between two subunits of the multisubunit enzyme complex, GPI-N-acetylglucosaminyltransferase (GPI-GnT), involved in the first step of GPI anchor biosynthesis in eukaryotes. Using mutational analysis, we show that the accessory subunits, GPI2 and GPI19, of GPI-GnT exhibit opposite effects on ergosterol biosynthesis and Ras signaling (which determines hyphal morphogenesis). This is because the two subunits negatively regulate one another; GPI19 mutants show up-regulation of GPI2, whereas GPI2 mutants show up-regulation of GPI19. Two different models were examined as follows. First, the two GPI-GnT subunits independently interact with ergosterol biosynthesis and Ras signaling. Second, the two subunits mutually regulate one another and thereby regulate sterol levels and Ras signaling. Analysis of double mutants of these subunits indicates that GPI19 controls ergosterol biosynthesis through ERG11 levels, whereas GPI2 determines the filamentation by cross-talk with Ras1 signaling. Taken together, this suggests that the first step of GPI biosynthesis talks to and regulates two very important pathways in C. albicans. This could have implications for designing new antifungal strategies.
机译:白色念珠菌是全球真菌感染的主要原因。它具有几种糖基磷脂酰肌醇(GPI)锚定的毒力因子。抑制GPI生物合成会减弱其毒力。在我们之前的工作的基础上,我们探讨了白色念珠菌中GPI生物合成与麦角固醇生物合成和菌丝形态发生的相互作用。这项研究也是多亚基酶复合物的两个亚基GPI-N-乙酰氨基葡萄糖氨基转移酶(GPI-GnT)之间存在转录共调控的首次报道,参与了真核生物中GPI锚定生物合成的第一步。使用突变分析,我们表明,GPI-GnT的辅助亚基GPI2和GPI19对麦角固醇的生物合成和Ras信号传导(决定菌丝形态发生)表现出相反的作用。这是因为两个亚基相互负调控。 GPI19突变体显示GPI2的上调,而GPI2突变体显示GPI19的上调。如下检查了两种不同的模型。首先,这两个GPI-GnT亚基独立地与麦角固醇的生物合成和Ras信号传导相互作用。第二,两个亚基相互调节,从而调节固醇水平和Ras信号传导。这些亚基的双突变体的分析表明,GPI19通过ERG11水平控制麦角固醇的生物合成,而GPI2通过与Ras1信号的串扰确定丝状化。综上所述,这表明GPI生物合成的第一步与白色念珠菌的两个非常重要的途径相关并对其进行调节。这可能对设计新的抗真菌策略有影响。

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