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作 者:郭振东[1] 侯小强[1] 何涛[1] 张维娜[1] 高玉伟[2] 汪莉[1] 王玉民[1]
机构地区:[1]军事医学科学院生物工程研究所,北京100071 [2]军事医学科学院军事兽医研究所,吉林长春130122
出 处:《生物技术通讯》2013年第2期147-152,共6页Letters in Biotechnology
基 金:国家自然科学基金(31100940);国家"重大新药创制"科技重大专项(2012ZX09J12106-03B)
摘 要:目的:预测靶向甲型流感病毒核蛋白(NP)基因的微小RNA(miRNA),并检测其对NP表达的影响。方法:从miRBase数据库中获取人成熟miRNA序列,利用miRanda软件预测潜在靶向流感病毒A/FM/1/47(H1N1)NP基因的人miRNA;通过双萤光素酶报告基因系统及Western印迹验证所预测的miRNA对NP表达的影响。结果:用miRanda软件在流感病毒A/FM/1/47(H1N1)NP基因上预测得到分值及最小结合自由能均较好的miR-769-3p;双萤光素酶报告基因结果显示miR-769-3p能显著降低报告基因载体萤光素酶的表达;Western印迹结果显示miR-769-3p能明显抑制NP的表达,但突变NP基因上的miR-769-3p结合位点后,miR-769-3p不能抑制NP的表达。结论:miR-769-3p可靶向流感病毒A/FM/1/47(H1N1)NP基因并抑制NP的表达,为抗甲型流感病毒的miRNA药物研发提供了依据和潜在药物靶标。Objective: To screen the candidate microRNA(miRNA) targeting the nucleoprotein(NP) of HIN1 influ- enza A virus by online tools, and analyze effect of the miRNA on NP expression by methods of biotechnology. Methods: Human mature miRNA sequences were downloaded from miRBase database, and miranda was used to predict the candidate miRNA targeting NP of A/FM/1/47(H1N1) from these sequences. The binding of miRNA with NP gene was tested by using dual-luciferase assays, and the effect of miRNA on NP expression was ana- lyzed by Western blotting. Results: With the excellent miranda score and minimal free energy, miR-769-3p was predicted as the most likely miRNA targeting NP gene. In lnciferase analysis, the NP reporter's luciferase activity dramatically decreased, which evidenced the binding of miR-769-3p with NP. Western blotting showed that the ex- pression of wild type NP was significantly suppressed by miR-769-3p, and this suppression did not occur when miR-769-3p targeting sites on NP were mutated. Conclusion: miR-769-3p can directly target NP of A/FM/1/47 (H1N1) and inhibit NP expression. Our study provide data basis and potential drug target for the development of new strategies for anti-influenza A virus intervention.
分 类 号:R373.13[医药卫生—病原生物学] Q78[医药卫生—基础医学]
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