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Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis

机译:通过新型茎环阵列RT-PCR分析检测siRNA介导的人细胞中靶标mRNA裂解活性

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摘要

The small interfering RNA (siRNA)-mediated target mRNA cleavage activity generates cleaved mRNA fragments with varied termini, which creates major technical challenges for the accurate and efficient detection and verification of cleavage sites on target mRNAs. Here we used a sensitive stem-loop array reverse transcription polymerase chain reaction (SLA-RT-PCR) approach to detect and verify the siRNA-mediated target mRNA cleavage sites by determining precise sequences at the 3′- termini of cleaved mRNA fragments in human cells under physiological conditions. Our results demonstrated the great potential and broad applications of using the SLA-RT-PCR as a sensitive, cost-efficient, and high-throughput tool to systematically detect siRNA-targeted mRNA cleavage sites and fragments in human cells.
机译:小干扰RNA(siRNA)介导的靶mRNA裂解活性产生具有可变末端的裂解的mRNA片段,这为准确,有效地检测和验证靶mRNA的裂解位点提出了重大技术挑战。在这里,我们使用敏感的茎-环阵列逆转录聚合酶链反应(SLA-RT-PCR)方法,通过确定人类裂解的mRNA片段3'-末端的精确序列来检测和验证siRNA介导的靶mRNA裂解位点细胞在生理条件下。我们的结果表明,使用SLA-RT-PCR作为灵敏,经济高效且高通量的工具来系统检测人细胞中siRNA靶向的mRNA裂解位点和片段的巨大潜力和广泛应用。

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