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Functional characterization of Fusarium verticillioides CPP1, a gene encoding a putative protein phosphatase 2A catalytic subunit

机译:镰刀菌镰刀菌的功能表征CPP1,一种编码推定蛋白磷酸酶2a催化亚基的基因

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Fusarium verticillioides produces the mycotoxin fumonisin B1 (FB1) on maize kernels. In this study, we identified a putative protein phosphatase gene CPP1 in F. verticillioides, and investigated its role in FB1 regulation. Previous work has shown that CPP1 expression is elevated in an FB1-suppressing genetic background. Thus, we hypothesized that CPP1 is negatively associated with FB1 production. To test this hypothesis, we generated a CPP1 knockout mutant, PP179, and studied the effects of gene deletion on FB1 biosynthesis and fungal development. PP179 showed elevated expression of FUM genes, and in turn produced higher levels of FB1 than the wild-type progenitor. Other significant mutant phenotypes included reduced radial growth on agar plates, reduced conidia germination rates, significantly increased macroconidia formation, and hyphal swelling. To verify that these phenotypes were directly due to CPP1 deletion, we complemented PP179 with the wild-type CPP1 gene. The complemented strain PPC4 showed FUM1 expression and FB1 production similar to that of the wild-type, providing evidence that CPP1 is negatively associated with FB1 biosynthesis. Other PP179 phenotypes, such as macroconidiation and hyphal swelling, were also restored to that of wild-type progenitor. Furthermore, we complemented F. verticillioides PP179 strain with Neurospora crassa wild-type ppe-1 gene, demonstrating that Cpp1 and PPE-1 proteins are functionally conserved. Pleiotropic effects of CPP1 deletion led us to hypothesize that CPP1 is associated with multiple downstream signalling pathways in F. verticillioides. Identification and functional characterization of downstream Cpp1-interacting proteins are necessary to better understand the complex regulatory mechanisms associated with Cpp1.
机译:镰刀菌在玉米核上产生霉菌毒素Fumonisin B1(FB1)。在这项研究中,我们鉴定了F. Verticillioides的推定蛋白磷酸酶基因Cpp1,并研究了其在FB1调节中的作用。以前的工作表明,CPP1表达式在FB1抑制遗传背景中提升。因此,我们假设CPP1与FB1生产负相关。为了测试这一假设,我们产生了CPP1敲除突变体,PP179,并研究了基因缺失对FB1生物合成和真菌发育的影响。 PP179显示出福温基因的表达升高,而且又产生比野生型祖细胞更高水平的FB1。其他显着的突变表型包括降低琼脂平板上的径向生长,降低了分枝瘤萌发率,显着增加了宏观经失症形成,悬垂性溶胀。为了验证这些表型直接由于CPP1缺失而直接,我们将PP179与野生型CPP1基因补充。补充的菌株PPC4显示了FUM1表达和与野生型类似的FB1产生,提供了CPP1与FB1生物合成呈负相关的证据。其他PP179表型,例如宏观致壬化和酸盐溶胀,也恢复到野生型祖细胞中。此外,通过Neurospora Crassa野生型PPE-1基因互补F. Verticillioids PP179菌株,证明CPP1和PPE-1蛋白在功能上保守。 CPP1删除的抗性效应LED指导我们假设CPP1与F. Verticillioides中的多个下游信号通路相关联。下游CPP1相互作用蛋白的鉴定和功能表征是为了更好地理解与CPP1相关的复杂调节机制。

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