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Demonstration of Loss of Heterozygosity by Single-Nucleotide Polymorphism Microarray Analysis and Alterations in Strain Morphology in Candida albicans Strains during Infection

机译:通过单核苷酸多态性微阵列分析和白色念珠菌菌株感染过程中菌株形态的改变来证明杂合性的丧失。

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Candida albicans is a diploid yeast with a predominantly clonal mode of reproduction, and no complete sexual cycle is known. As a commensal organism, it inhabits a variety of niches in humans. It becomes an opportunistic pathogen in immunocompromised patients and can cause both superficial and disseminated infections. It has been demonstrated that genome rearrangement and genetic variation in isolates of C. albicans are quite common. One possible mechanism for generating genome-level variation among individuals of this primarily clonal fungus is mutation and mitotic recombination leading to loss of heterozygosity (LOH). Taking advantage of a recently published genome-wide single-nucleotide polymorphism (SNP) map (A. Forche, P. T. Magee, B. B. Magee, and G. May, Eukaryot. Cell 3:705-714, 2004), an SNP microarray was developed for 23 SNP loci residing on chromosomes 5, 6, and 7. It was used to examine 21 strains previously shown to have undergone mitotic recombination at the GAL1 locus on chromosome 1 during infection in mice. In addition, karyotypes and morphological properties of these strains were evaluated. Our results show that during in vivo passaging, LOH events occur at observable frequencies, that such mitotic recombination events occur independently in different loci across the genome, and that changes in karyotypes and alterations of phenotypic characteristics can be observed alone, in combination, or together with LOH.
机译:白色念珠菌是一种二倍体酵母,具有主要的克隆繁殖方式,尚无完整的性周期。作为一种共生生物,它栖息于人类的各种生态位中。它在免疫功能低下的患者中成为机会病原体,可引起浅表性和弥漫性感染。已经证明 C分离株的基因组重排和遗传变异。白化病很常见。在这种主要克隆真菌的个体之间产生基因组水平变异的一种可能机制是突变和有丝分裂重组,导致杂合性(LOH)丧失。利用最近发布的全基因组单核苷酸多态性(SNP)图(A. Forche,PT Magee,BB Magee,and G.May,Eukaryot。Cell 3:705-714,2004),开发了SNP微阵列用于检测位于5号,6号和7号染色体上的23个SNP位点。它被用来检查先前在小鼠中感染期间在21号染色体上的 GAL1 位点经历过有丝分裂重组的21个菌株。另外,评估了这些菌株的核型和形态学特性。我们的结果表明,在体内传代过程中,LOH事件以可观察的频率发生,这种有丝分裂重组事件在整个基因组的不同基因座中独立发生,并且可以单独,组合或一起观察到核型的改变和表型特征的改变。与LO。

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