Cloning and Expression of Gynecophoral Canal Protein Gene of Schistosoma japonicum (Chinese strain)

JIN Ya-Mei1,2, LIN Jiao-Jiao1, FENG Xin-Gang, ZHANG Liang1, WU Xiang-Fu2,ZHOU Yuan-Cong2,CAI You-Min£±*
( 1Shanghai Institute of Animal Parasitology, Chinese Academy of Agricultural Science, Key Laboratory of Animal Parasitology, Ministry of Agriculture of China, Shanghai 200232,China; 2Institute of Biochemistry and Cell Biology, Shanghai Institute for Biological Sciences,the Chinese Academy of Sciences, Shanghai 200031,China )

Abstract    A 1949 bp cDNA fragment was amplified by RT-PCR from adult Schistosoma japonicum (Chinese strain) mRNA with 3 pair of primers that were designed according to published SmGCP gene encoding gynecophoral canal protein of Schistosoma mansoni and SjGCP1 gene encoding the conservative region of gynecophoral canal protein of Schistosoma japonicum.Sequence analysis indicated that this fragment, named SjGCP,with 85% identity to SmGCP, contained a complete open reading frame (ORF) of gynecophoral canal protein gene of Schistosoma japonicum (Chinese strain).The amino acid sequence shared 83.7% identity with gynecophoral canal protein of Schistosoma mansoni.This fragment was cloned into the expression vector pET28c(+) and subsequently expressed in Escherichiacoli.SDS-PAGE revealed that the molecular weight of this expressed product was 80 kD.Western blotting showed that the recombinant protein reacted well with the rabbit serum immunized with Sj worm antigen,indicating that this expressed product had good antigenicity.
Key words    Schistosoma japonicum; gynecophoral canal protein; gene cloning; gene expression

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