Karuppayil S M, Peng M, Mendoza L, Levins T A, Szaniszlo P J
Department of Microbiology, University of Texas at Austin, USA.
J Med Vet Mycol. 1996 Mar-Apr;34(2):117-25. doi: 10.1080/02681219680000181.
Primers having designs based on highly conserved stretches in the deduced amino acid sequences of chitin synthase (CHS) genes were used in PCR reactions to amplify 600 bp and 366 bp products from the genomic DNA of three major causal agents of chromoblastomycosis. Cloning and sequencing of the PCR products of one of these fungi, Fonsecaea pedrosoi, identified three CHS sequences designated as FpCHS1, FpCHS2 and FpCHS3. FpCHS1 and FpCHS2 were homologous to regions of CHS1 and CHS2 of Saccharomyces cerevisiae, and their derived amino acid sequences fell into chitin synthase classes I and II, respectively. FpCHS3 was homologous to a region of the CAL1/CSD2 gene of S. cerevisiae, which codes for the chitin synthase three (Chs3) enzyme in that fungus. Phylogenetic trees constructed using the deduced amino acid sequences of PCR-amplified CHS products from many fungi clustered F. pedrosoi with other dematiaceous fungi, providing new molecular evidence for the genetic relatedness of these organisms. The identification of these CHS genes in F. pedrosoi will facilitate future studies of the functional roles of chitin synthases in the unique in vivo dimorphism exhibited by chromoblastomycotic fungi.
基于几丁质合酶(CHS)基因推导氨基酸序列中高度保守区域设计的引物,用于聚合酶链反应(PCR),以从三种主要着色芽生菌病病原体的基因组DNA中扩增出600 bp和366 bp的产物。对其中一种真菌裴氏着色霉(Fonsecaea pedrosoi)的PCR产物进行克隆和测序,鉴定出三个CHS序列,分别命名为FpCHS1、FpCHS2和FpCHS3。FpCHS1和FpCHS2分别与酿酒酵母(Saccharomyces cerevisiae)的CHS1和CHS2区域同源,其推导的氨基酸序列分别属于几丁质合酶I类和II类。FpCHS3与酿酒酵母CAL1/CSD2基因的一个区域同源,该基因在该真菌中编码几丁质合酶三(Chs3)酶。使用来自多种真菌的PCR扩增CHS产物的推导氨基酸序列构建的系统发育树,将裴氏着色霉与其他暗色丝孢菌聚集在一起,为这些生物体的遗传相关性提供了新的分子证据。在裴氏着色霉中鉴定出这些CHS基因,将有助于未来研究几丁质合酶在着色芽生菌病真菌独特的体内双态性中所起的功能作用。