Carr J, Shearer G
Department of Biological Sciences, Center for Molecular & Cellular Biosciences, The University of Southern Mississippi, Hattiesburg, Mississippi 39406, USA.
J Bacteriol. 1998 Dec;180(24):6697-703. doi: 10.1128/JB.180.24.6697-6703.1998.
The genome size, complexity, and ploidy of the dimorphic pathogenic fungus Histoplasma capsulatum was determined by using DNA renaturation kinetics, genomic reconstruction, and flow cytometry. Nuclear DNA was isolated from two strains, G186AS and Downs, and analyzed by renaturation kinetics and genomic reconstruction with three putative single-copy genes (calmodulin, alpha-tubulin, and beta-tubulin). G186AS was found to have a genome of approximately 2.3 x 10(7) bp with less than 0.5% repetitive sequences. The Downs strain, however, was found to have a genome approximately 40% larger with more than 16 times more repetitive DNA. The Downs genome was determined to be 3.2 x 10(7) bp with approximately 8% repetitive DNA. To determine ploidy, the DNA mass per cell measured by flow cytometry was compared with the 1n genome estimate to yield a DNA index (DNA per cell/1n genome size). Strain G186AS was found to have a DNA index of 0.96, and Downs had a DNA index of 0.94, indicating that both strains are haploid. Genomic reconstruction and Southern blot data obtained with alpha- and beta-tubulin probes indicated that some genetic duplication has occurred in the Downs strain, which may be aneuploid or partially diploid.
通过DNA复性动力学、基因组重建和流式细胞术,确定了二态性致病真菌荚膜组织胞浆菌的基因组大小、复杂性和倍性。从G186AS和Downs这两个菌株中分离出核DNA,并使用三个假定的单拷贝基因(钙调蛋白、α-微管蛋白和β-微管蛋白)通过复性动力学和基因组重建进行分析。发现G186AS的基因组约为2.3×10⁷ bp,重复序列少于0.5%。然而,Downs菌株的基因组大约大40%,重复DNA多出16倍以上。Downs基因组被确定为3.2×10⁷ bp,约有8%的重复DNA。为了确定倍性,将通过流式细胞术测量的每个细胞的DNA质量与1n基因组估计值进行比较,得出DNA指数(每个细胞的DNA/1n基因组大小)。发现G186AS菌株的DNA指数为0.96,Downs菌株的DNA指数为0.94,表明这两个菌株都是单倍体。用α-和β-微管蛋白探针获得的基因组重建和Southern印迹数据表明,Downs菌株中发生了一些基因重复,可能是非整倍体或部分二倍体。