›› 2014, Vol. 32 ›› Issue (2): 3-95-100.

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Cloning, Expression and Transcription Specificity Analysis of Two Tyrosinases from Schistosoma japonicum

LI Na-na1,WANG Ji-peng2,3 *,DU Xiao-feng2,3,HU Wei2,3   

  1. 1 State Key Laboratory of Bioreactor Engineering,East China University of Science and Technology,Shanghai 200237,China;2 National Institute of Parasitic Diseases,Chinese Center for Disease Control and Prevention;Key Laboratory of Parasite and Vector Biology,Ministry of Health;WHO Collaborating Centre for Malaria, Schistosomiasis and Filariasis, Shanghai 200025,China;3 Department of Microbiology and Microbial Engineering,School of Life Sciences,Fudan University,Shanghai 200433,China
  • Online:2014-04-30 Published:2014-07-03

Abstract: Objective  To clone and express the recombinant proteins based on the whole open reading frame of two tyrosinases(tyrosinase 1 and tyrosinase 2) from Schistosoma japonicum, and study the transcription specificity of the two tyrosinases in different sex and developmental stages of S. japonicum.  Methods  The full-length of SjTYR1 and SjTYR2 were amplified with specific primers and subcloned into pSJ2. The recombinant plasmids were transformed into E. coli Rosetta Gami strains and induced with IPTG for expression. The recombinant proteins were purified by Ni-NTA agarose. The recombinant proteins SjTYR1 and SjTYR2 were used to produce the specific antibodies by immunizing the rabbits. The immunogenicity of the recombinant proteins SjTYR1 and SjTYR2 were detected by Western blotting using sera of recombinant proteins-immunized rabbits and S. japonicum-infected rabbit serum as the primary antibody, respectively. The reactivity of sera from recombinant proteins-immunized rabbits was analyzed by Western blotting against the native protein of S. japonicum worm. Total RNA was extracted from 14, 16, 18, 20, 22, 24, 26, and 28-day male and female worms. Transcription levels of the two tyrosinases in different sex and different stage were determined via RT-PCR method.  Results  The expression vector of SjTYR1/pSJ2 and SjTYR2/pSJ2 were constructed and the recombinant proteins SjTYR1 and SjTYR2 were expressed in inclusion body in E. coli(about Mr 55 000 and Mr 56 800). The sera of S. japonicum-infected rabbits reacted positively with the purified recombinant protein SjTYR1, but not with recombinant protein SjTYR2. The native protein of S. japonicum worm could be recognized by sera of rSjTYR1-immunized rabbits (Mr 100 000), but not by sera of rSjTYR2-immunized rabbits. Transcription levels of the two tyrosinases in male worms were nearly zero. In female worms, the transcription levels of the two tyrosinases increased sharply from the 24th day post-infection and reached maximum on the 28th day.  Conclusion  The recombinant proteins of SjTYR1 and SjTYR2 show immunogenicity and immunoreactivity. SjTYR1 and SjTYR2 are both expressed specifically in female worms and the transcription levels increase in 24-28 days after infection.

Key words: Schistosoma japonicum, Tyrosinase, Clone, Expression, Transcription specificity