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哺乳动物RNA聚合酶III启动子H1可在鸡细胞中转录诱导RNA干扰的短发夹RNA。

Mammalian Pol III promoter H1 can transcribe shRNA inducing RNAi in chicken cells.

作者信息

Yuan Jing, Wang Xiaobo, Zhang Ying, Hu Xiaoxiang, Fei Jing, Li Ning

机构信息

State Key Laboratory for Agrobiotechnology, China Agricultural University, No. 2 Yuanmingyuan West Rd, Haidian District, Beijing, 100094, P.R. China.

出版信息

Mol Biol Rep. 2006 Mar;33(1):33-41. doi: 10.1007/s11033-006-0002-y.

Abstract

Double-stranded RNA-mediated interference (RNAi) has recently emerged as a powerful reverse genetic tool to silence gene expression in multiple organisms. RNAi based on DNA vector is not sufficiently established in chicken species. The present study was performed to evaluate RNAi induced by shRNA transcribed from mammalian Pol III promoter H1 in the chicken cells by using a dual fluorescence reporter assay, a plasmid encoding GFP and a plasmid encoding RFP. The evaluation of RNAi efficiency was performed in two kinds of chicken cell type: primary CEF cells and chicken DT-40 cells by lipofection. GFP- and RFP-expressing cells were observed under fluorescent microscopy, and their mRNAs content were analyzed by quantitative RT-PCR. The intensity of the green fluorescence generated by GFP was greatly suppressed by human H1 promoter transcribed GFP-shRNA. Quantitative RT-PCR analysis showed that normalized GFP mRNA expression was reduced to 37 and 32 in primary CEF and DT-40 cells, respectively. In contrast to GFP, the intensity of the red fluorescence generated by RFP protein and the RFP mRNA levels remained unchanged. Consequently, it was concluded that the RNAi induced by shRNA transcribed from mammalian Pol III promoter H1 is applicable to suppress the gene expression specifically and efficiently in chicken cells.

摘要

双链RNA介导的干扰(RNAi)最近已成为一种强大的反向遗传学工具,可在多种生物体中沉默基因表达。基于DNA载体的RNAi在鸡物种中尚未得到充分确立。本研究通过使用双荧光报告基因检测、编码绿色荧光蛋白(GFP)的质粒和编码红色荧光蛋白(RFP)的质粒,评估了在鸡细胞中由哺乳动物RNA聚合酶III启动子H1转录的短发夹RNA(shRNA)诱导的RNAi。通过脂质转染在两种鸡细胞类型中进行RNAi效率评估:原代鸡胚成纤维细胞(CEF细胞)和鸡DT-40细胞。在荧光显微镜下观察表达GFP和RFP的细胞,并通过定量逆转录聚合酶链反应(qRT-PCR)分析它们的mRNA含量。由人H1启动子转录的GFP-shRNA极大地抑制了GFP产生的绿色荧光强度。qRT-PCR分析表明,在原代CEF细胞和DT-40细胞中,标准化的GFP mRNA表达分别降至37和32。与GFP相反,RFP蛋白产生的红色荧光强度和RFP mRNA水平保持不变。因此,得出结论,由哺乳动物RNA聚合酶III启动子H1转录的shRNA诱导的RNAi适用于在鸡细胞中特异性且有效地抑制基因表达。

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