Wada M, Kitada K, Saito M, Egawa K, Nakamura Y
Department of Tumor Biology, University of Tokyo, Japan.
J Infect Dis. 1993 Oct;168(4):979-85. doi: 10.1093/infdis/168.4.979.
The major surface glycoprotein (MSG) of Pneumocystis carinii plays a crucial role in the pathobiology of P. carinii, which often causes fatal pneumonia in AIDS patients. The cDNAs encoding MSG antigens were cloned from a lambda gt11 expression library of rat-derived P. carinii by immunoscreening. The cloned cDNAs constituted a gene family containing approximately 70% amino acid identity between subtypes. The diversity of MSG cDNAs was high and reflected the genomic structure of MSG genes clustered in the P. carinii chromosomes. These multiple genes may account for the high-level expression of MSG that could generate potential variations in the cell surface. Moreover, the MSG sequences have significant sequence homology to tropomyosins and myosins, suggesting physical or functional association with the membrane cytoskeleton.
卡氏肺孢子虫的主要表面糖蛋白(MSG)在卡氏肺孢子虫的病理生物学中起着关键作用,卡氏肺孢子虫常导致艾滋病患者发生致命性肺炎。通过免疫筛选从大鼠源性卡氏肺孢子虫的λgt11表达文库中克隆了编码MSG抗原的cDNA。克隆的cDNA构成了一个基因家族,各亚型之间氨基酸同一性约为70%。MSG cDNA的多样性很高,反映了聚集在卡氏肺孢子虫染色体上的MSG基因的基因组结构。这些多个基因可能解释了MSG的高水平表达,而这种表达可能会在细胞表面产生潜在变异。此外,MSG序列与原肌球蛋白和肌球蛋白具有显著的序列同源性,提示其与膜细胞骨架存在物理或功能关联。