Isolation of Cryptococcus neoformans chromosome-specific probes using expressed sequence tags.

S. Spitzer, E. Spitzer
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引用次数: 2

Abstract

Clinical and environmental isolates of Cryptococcus neoformans exhibit a high degree of karyotypic variability. Analysis of the molecular basis of karyotypic differences requires a large set of chromosome-specific probes. We have determined the chromosomal distribution of a set of randomly selected C. neoformans cDNA clones and have explored the feasibility of identifying these clones through partial DNA sequencing. Forty-four randomly selected cDNA clones were labelled and hybridized to PFGE blots of C. neoformans. Expressed sequence tags were generated by sequencing the 5'-end of each clone. Thirty-five clones hybridized to single bands on PFGE blots. At least seven chromosomes were recognized by these probes. Homology searches identified potential homologs of several groups of proteins not previously studied in C. neoformans. PFGE hybridization and sequencing of random cDNA clones is an efficient method for identifying chromosomal-specific probes in fungi that lack extensive sets of genetic markers.
利用表达序列标签分离新型隐球菌染色体特异性探针。
临床和环境分离的新型隐球菌表现出高度的核型变异性。分析核型差异的分子基础需要大量的染色体特异性探针。我们已经确定了一组随机选择的新形态C. cDNA克隆的染色体分布,并探讨了通过部分DNA测序鉴定这些克隆的可行性。将44个随机选择的cDNA克隆标记并杂交到新生C.的PFGE印迹上。通过对每个克隆的5'端进行测序,生成表达序列标签。35个克隆在PFGE印迹上杂交成单条带。这些探针至少识别了7条染色体。同源性搜索确定了以前未在新生c中研究过的几组蛋白质的潜在同源性。PFGE杂交和随机cDNA克隆测序是鉴定真菌中缺乏广泛遗传标记的染色体特异性探针的有效方法。
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