Journal of Southern Medical University ›› 2004, Vol. 24 ›› Issue (08): 869-872.

Previous Articles     Next Articles

Cloning and analysis of the promoter region of Schistosoma japonicum 8k CaBP gene

PENG Hong-juan, CHEN Xiao-guang, ZHOU Xiao-hong, SHEN Shu-man   

  1. 第一军医大学寄生虫学教研室, 广东, 广州, 510515
  • Online:2004-08-20 Published:2004-08-20

Abstract: Objective To clone and analyze the promoter sequence of Schistosoma japonicum 8k Calcium binding protein(CaBP) (Sj8CaBP) gene. Methods The genomic DNA was extracted from S. japonicum adult worms. The DNA library was constructed according to the user’s manual for Clontech Universal Genome WalkerTM Kit, and the gene-specific primer 1 and 2 (GSP1 and GSP2) of Sj8CaBP gene were designed and synthesized. GSP1 and GSP2 were coupled with the adaptor primer 1 and 2 (AP1 and AP2), then nested PCR was performed. After proper purification, the PCR product was linked to pMD-18 T vector, and the recombinant T-vector was sequenced, analyzed with the promoter prediction software and compared with the cDNA sequence of Sj8CaBP. Results The cloned Sj8CaBP gene was about 1 079 bp in length (GenBank accession No.AY262018), which contained a full open-reading frame with 1 intron and 2 exons. The 5’UTR has a putative promoter region including a TATA-box and a CCAAT-box. The GC-box binding region was not found in this gene, nor was that for active protein 1 (AP-1) often seen in other schistosome genes. Conclusion A 1 079 bp Sj8CaBP gene fragment (GenBank accession No.AY262018) was obtained from a S. japonicum genomic DNA library, containing a promoter region with TATA-box, CCAAT-box, 1 intron and 2 extrons.

CLC Number: