The cleavage of PreC/C mRNA of HBV in vitro by a 10-23 DNA zyme
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摘要: 探讨 10 - 2 3DNA酶对HBV前C/C区mRNA的体外切割活性。用克隆及亚克隆技术将HepG2 2 15细胞中HBV前C/C区基因克隆入pCDNA3 1(+)载体 ,转录表达该区mRNA。合成针对HBV前C/C区 2 0 31位点的 10 -2 3DNA酶 ,观察其对靶mRNA的切割活性。 10 - 2 3DNA酶对HBV前C/C区mRNA的切割效率与Mg2 + 离子浓度呈正相关。 10 - 2 3DNA酶能有效切割HBV前C/C区mRNA。Abstract: To explore the use of synthetic 10-23DNA zyme targeted to PreC/C mRNA as potential therapy for hepatitis B, pCDNA3.1 (+) -Pre C/C vector was established for transcriping target mRNA. Synthesize a 10-23 DNA zyme corresponding to 2031 point of HBV PreC/C mRNA and observe its catalytic activity in vitro. Our results show that synthetic 10-23DNA zyme can efficiently cleave target mRNA in vitro, and its activity is dependent on the concentration of Mg 2+ ion.
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Key words:
- DNA zyme /
- hepatitis B virus
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