Nash T E, Mowatt M R
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Mol Biochem Parasitol. 1992 Apr;51(2):219-27. doi: 10.1016/0166-6851(92)90072-r.
Giardia lamblia undergoes surface antigenic variation. The variant-specific surface proteins (VSPs) of isolate WB are cysteine-rich, can vary dramatically in size, contain Cys-X-X-Cys motifs, and are differentially expressed. GS/M(H7) is a Giardia clone from a different isolate which expresses a VSP epitope not found in WB. The VSP gene encoding this epitope was selected by differential hybridization using radiolabeled cDNA from H7 and variant sibling trophozoite lines from the same isolate that express other VSPs. The VSPH7 gene probe detects an 1800 nucleotide transcript abundant in H7 but undetectable in variant siblings. Primer extension directly from RNA was used to complete the gene sequence which predicted a protein with a molecular weight of 56,832. The protein showed many of the characteristics of 2 previously sequenced WB VSPs including many Cys-X-X-Cys tetrapeptides and a conserved carboxy-terminal region. Genomic Southern analysis indicated the presence of 2 distinct VSPH7 genes in H7. An oligonucleotide from the conserved region was used in combination with one specific for the VSPH7 gene to estimate the VSP repertoire size at between 133 and 151. VSPs, even from isolates expressing unique epitopes, constitute a family of related proteins.
蓝氏贾第鞭毛虫会发生表面抗原变异。分离株WB的变异特异性表面蛋白(VSPs)富含半胱氨酸,大小差异很大,含有Cys-X-X-Cys基序,且表达存在差异。GS/M(H7)是来自不同分离株的蓝氏贾第鞭毛虫克隆,它表达一种在WB中未发现的VSP表位。通过使用来自H7的放射性标记cDNA以及来自同一分离株表达其他VSPs的变异同胞滋养体系进行差异杂交,选择了编码该表位的VSP基因。VSPH7基因探针可检测到在H7中丰富但在变异同胞中无法检测到的1800个核苷酸的转录本。直接从RNA进行引物延伸用于完成基因序列,该序列预测的蛋白质分子量为56,832。该蛋白质具有许多先前测序的WB VSPs的特征,包括许多Cys-X-X-Cys四肽和一个保守的羧基末端区域。基因组Southern分析表明H7中存在2个不同的VSPH7基因。来自保守区域的寡核苷酸与VSPH7基因特异性的寡核苷酸结合使用,估计VSP库大小在133至151之间。即使来自表达独特表位的分离株,VSPs也构成一个相关蛋白质家族。