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Development of a new duplex real-time polymerase chain reaction assay for detection of dicer in G. gallus

机译:新型双链实时聚合酶链反应检测试剂盒的检测

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摘要

Recently, there has been a growing body of evidence showing that cellular microRNAs (miRNAs) are involved in virus-host interactions. Numerous studies have focused on analyses of the expression profiles of cellular miRNAs, but the expression patterns of Dicer, which is responsible for the generation of miRNAs, have only rarely been explored in Gallus gallus. We developed a duplex realtime reverse transcriptase polymerase chain reaction (RTPCR) assay for the relative quantification of the mRNAs of Dicer and β-actin in G. gallus. To apply this method, the expression of Dicer in avian cells after infection with avian leukosis virus subgroup J (ALV-J) was detected using our established duplex real-time RT-PCR. The duplex realtime RT-PCR assay is sufficiently sensitive, specific, accurate, reproducible, and cost-effective for the detection of Dicer in G. gallus. Furthermore, this study, for the first time, demonstrated that ALV-J can induce differential expression of Dicer mRNA in the ALV-J-infected cells.
机译:最近,越来越多的证据表明细胞微RNA(miRNA)参与了病毒-宿主相互作用。许多研究都集中在分析细胞miRNA的表达谱上,但负责miRNA生成的Dicer的表达模式很少在鸡内被研究。我们开发了一种双工实时逆转录酶聚合酶链反应(RTPCR)分析法,用于相对定量地测定G. gallus中Dicer和β-actin的mRNA。为了应用此方法,使用我们建立的双工实时RT-PCR检测了感染了禽白血病J亚组(ALV-J)的Dicer在禽细胞中的表达。双重实时RT-PCR测定对于灵芝中Dicer的检测足够灵敏,特异,准确,可重复且具有成本效益。此外,该研究首次证明ALV-J可以诱导ALV-J感染的细胞中Dicer mRNA的差异表达。

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