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彭寨玉, 余新炳, 吴忠道, 徐劲, 吴德, 李孜. 日本血吸虫酪蛋白激酶Ⅱβ亚基的序列分析[J]. 中国公共卫生, 2003, 19(10): 1174-1176.
引用本文: 彭寨玉, 余新炳, 吴忠道, 徐劲, 吴德, 李孜. 日本血吸虫酪蛋白激酶Ⅱβ亚基的序列分析[J]. 中国公共卫生, 2003, 19(10): 1174-1176.
PENG Zhai-yi, YU Xin-bing, WU Zhong-dao, . Cloning and sequence analysis on casein kinase Ⅱ beta subunit of sohistosoma japonicum[J]. Chinese Journal of Public Health, 2003, 19(10): 1174-1176.
Citation: PENG Zhai-yi, YU Xin-bing, WU Zhong-dao, . Cloning and sequence analysis on casein kinase Ⅱ beta subunit of sohistosoma japonicum[J]. Chinese Journal of Public Health, 2003, 19(10): 1174-1176.

日本血吸虫酪蛋白激酶Ⅱβ亚基的序列分析

Cloning and sequence analysis on casein kinase Ⅱ beta subunit of sohistosoma japonicum

  • 摘要:
      目的   发现并克隆日本血吸虫新基因。
      方法   对已获得的日本血吸虫表达序列标签(EST)进行同源性分析, 识别血吸虫新基因; 根据EST设计引物, 用3'RACE从mRNA中扩增获得新基因全长, 用生物信息学技术对获得的编码基因进行结构与功能分析, 将新基因的完整编码阅读框克隆入原核表达载体pGEX-4T-1。
      结果   用3'RACE获得一个EST的3'端所缺序列, 得到完整编码阅读框, 其开放阅读框(ORF)654bp, 编码217个氨基酸。利用生物信息学技术确定其为日本血吸虫酪蛋白激酶Ⅱβ亚单位的编码基因。重组质粒经双酶切及测序鉴定, 证明日本血吸虫CKⅡβ原核表达质粒构建成功。
      结论   扩增并成功克隆日本血吸虫酪蛋白激酶Ⅱβ亚单位编码基因的全长cDNA, 为进一步的功能研究打下基础。

     

    Abstract:
      Objective   To recognize and clone the novel genes of Schistosoma japonicum (Sj).
      Methods   The ESTs obtained in our laboratory were analyzed by homologous searching, the novel genes were recognized. Accor ding to the interested EST, the full-length cDNA of the novel gene was obtained by 3' RACE PCR. The cDNA sequence were cloned into pGEX-4T-1 vector and analyzed by bioinformatics.
      Results   A new cDNA sequence was obtained, the sequence contains a fulllength sequence with 654bp ORF, which encoded 217 amino acid residues. The new gene was identified to be the gene encoding casein kinase Ⅱ beta subunit. The sequences were cloned into pGEX-4T-1 vector and identified by restriction analysis and sequencing.
      Conclusion   The full-length cDNA sequences encoding Sj casein kinase Ⅱ beta subunit were firstly sequenced and cloned, which give the basis for further study.

     

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