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Genes transactivated by hepatitis C virus core protein a microarray assay

机译:由丙型肝炎病毒核心蛋白反式激活的基因微阵列分析

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摘要

AIM: To explore the new target genes transactivated by hepatitis C virus (HCV) core protein and to elucidate the pathogenesis of HCV infection.METHODS: Reverse transcribed cDNA was subjected to microarray assay. The coding gene transactivated by HCV core protein was cloned and analyzed with bioinformatics methods.RESULTS: The expressive vector of pcDNA3.1(-)-core was constructed and confirmed by restriction enzyme digestion and DNA sequencing and approved correct. mRNA was purified from HepG2 and HepG2 cells transfected with pcDNA3.1(-)-core, respectively. The cDNA derived was subjected to microarray assay. A new gene named HCTP4 was cloned with molecular biological method in combination with bioinformatics method.CONCLUSION: HCV core is a potential transactivator. Microarray is an efficient and convenient method for analysis of differentially expressed genes.
机译:目的:探讨丙型肝炎病毒(HCV)核心蛋白反式激活的新靶基因,并阐明HCV感染的发病机制。方法:对逆转录cDNA进行微阵列分析。结果:构建了pcDNA3.1(-)-核心表达载体,经限制性内切酶消化和DNA测序鉴定,证实正确。从分别转染了pcDNA3.1(-)-核心的HepG2和HepG2细胞中纯化mRNA。对衍生的cDNA进行微阵列分析。分子生物学方法结合生物信息学方法,成功克隆了一个新的HCTP4基因。结论:HCV核心是一种潜在的反式激活因子。芯片是分析差异表达基因的一种有效而便捷的方法。

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