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Characterization of the Chromosome 4 Genes That Affect Fluconazole-Induced Disomy Formation in Cryptococcus neoformans

机译:影响氟康唑诱导的新隐球菌二体形成的染色体4基因的表征。

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摘要

Heteroresistance in Cryptococcus neoformans is an intrinsic adaptive resistance to azoles and the heteroresistant phenotype is associated with disomic chromosomes. Two chromosome 1 (Chr1) genes, ERG11, the fluconazole target, and AFR1, a drug transporter, were reported as major factors in the emergence of Chr1 disomy. In the present study, we show Chr4 to be the second most frequently formed disomy at high concentrations of fluconazole (FLC) and characterize the importance of resident genes contributing to disomy formation. We deleted nine Chr4 genes presumed to have functions in ergosterol biosynthesis, membrane composition/integrity or drug transportation that could influence Chr4 disomy under FLC stress. Of these nine, disruption of three genes homologous to Sey1 (a GTPase), Glo3 and Gcs2 (the ADP-ribosylation factor GTPase activating proteins) significantly reduced the frequency of Chr4 disomy in heteroresistant clones. Furthermore, FLC resistant clones derived from sey1Δglo3Δ did not show disomy of either Chr4 or Chr1 but instead had increased the copy number of the genes proximal to ERG11 locus on Chr1. Since the three genes are critical for the integrity of endoplasmic reticulum (ER) in Saccharomyces cerevisiae, we used Sec61ß-GFP fusion as a marker to study the ER in the mutants. The cytoplasmic ER was found to be elongated in sey1Δ but without any discernable alteration in gcs2Δ and glo3Δ under fluorescence microscopy. The aberrant ER morphology of all three mutant strains, however, was discernable by transmission electron microscopy. A 3D reconstruction using Focused Ion Beam Scanning Electron Microscopy (FIB-SEM) revealed considerably reduced reticulation in the ER of glo3Δ and gcs2Δ strains. In sey1Δ, ER reticulation was barely detectable and cisternae were expanded extensively compared to the wild type strains. These data suggest that the genes required for maintenance of ER integrity are important for the formation of disomic chromosomes in C. neoformans under azole stress.
机译:新型隐球菌的异抗性是对唑类的固有适应性抗性,并且异抗性表型与二体染色体相关。据报道,两个染色体1(Chr1)基因ERG11是氟康唑的靶标,而AFR1是药物转运蛋白,是导致Chr1二体化的主要因素。在本研究中,我们显示Chr4在高浓度的氟康唑(FLC)下是第二频繁形成的二体性,并表征了促进二体性形成的常驻基因的重要性。我们删除了可能在麦角固醇生物合成,膜组成/完整性或药物运输中具有功能的9个Chr4基因,这些基因可能会影响FLC胁迫下的Chr4二体化。在这九个基因中,与Sey1(GTPase),Glo3和Gcs2(ADP-核糖基化因子GTPase活化蛋白)同源的三个基因的破坏显着降低了异抗性克隆中Chr4二体化的频率。此外,源自sey1Δglo3Δ的FLC抗性克隆没有显示Chr4或Chr1的二体性,而是增加了Chr1上ERG11基因座附近基因的拷贝数。由于这三个基因对于酿酒酵母内质网(ER)的完整性至关重要,因此我们使用Sec61ß-GFP融合蛋白作为标记来研究突变体中的ER。发现在荧光显微镜下,胞质ER在sey1Δ中延长,但在gcs2Δ和glo3Δ中没有任何明显的改变。然而,通过透射电子显微镜可辨别所有三个突变菌株的异常ER形态。使用聚焦离子束扫描电子显微镜(FIB-SEM)进行的3D重建显示,glo3Δ和gcs2Δ菌株的ER的网状结构大大降低。在sey1Δ中,与野生型菌株相比,几乎无法检测到ER网状结构,并且水箱得到了广泛的扩展。这些数据表明,维持ER完整性所需的基因对于在吡咯胁迫下新形成梭状芽孢杆菌的二体染色体形成非常重要。

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