Chua S S, Momany M, Mendoza L, Szaniszlo P J
Department of Microbiology, University of Texas at Austin 78712-1095.
Curr Microbiol. 1994 Sep;29(3):151-6. doi: 10.1007/BF01570756.
Degenerate PCR primers were used to amplify a 600-bp conserved gene region for chitin synthases from genomic DNA of Sporothrix schenckii, a dimorphic fungal pathogen of humans and animals. Three chitin synthase gene homologs were amplified as shown by DNA sequence analysis and by Southern blotting experiments. Based on differences among the predicted amino acid sequences of these homologs, each was placed within one of three different chitin synthase classes. Phylogenies constructed with the sequences and the PAUP 3.1.1 program showed that S. schenckii consistently clustered most closely with Neurospora crassa in each of the three chitin synthase classes. These findings are significant because the phylogenies support by a new method the grouping of the imperfect fungus S. schenckii with the Pyrenomycetes of the Ascomycota.
简并PCR引物用于从申克孢子丝菌(一种人和动物的双态真菌病原体)的基因组DNA中扩增出一段600bp的几丁质合酶保守基因区域。通过DNA序列分析和Southern印迹实验表明,扩增出了三个几丁质合酶基因同源物。根据这些同源物预测氨基酸序列的差异,每个同源物被归入三个不同几丁质合酶类别中的一类。用这些序列和PAUP 3.1.1程序构建的系统发育树表明,在三个几丁质合酶类别中,申克孢子丝菌始终与粗糙脉孢菌聚类关系最为密切。这些发现具有重要意义,因为系统发育树用一种新方法支持了将不完全真菌申克孢子丝菌与子囊菌门的核菌纲归为一组。