Inhibition of EGFP expression by siRNA in EGFP-stably expressing Huh-7 cells

被引:24
作者
Cao, MM [1 ]
Ren, H [1 ]
Pan, X [1 ]
Pan, W [1 ]
Qi, ZT [1 ]
机构
[1] Second Mil Med Univ, Dept Microbiol, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA interference (RNAi); short interfering RNA (siRNA); in vitro transcription; enhanced green fluorescent protein (EGFP); gene expression;
D O I
10.1016/j.jviromet.2004.03.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The RNA interference (RNAi) is a powerful tool to silence gene expression post-transcriptionally, and causes the degradation of an mRNA containing the same sequence. In this present study, an alternative approach was used to in vitro synthesize enhanced green fluorescent protein (EGFP) specific short interfering RNA (siRNA) using T7 RNA polymerase, and a pEGFP-N1 transfected, human hepatoma cell line Huh-7 derived Huh-7-N cell clone was established. When introduced the siRNA into the EGFP expressing Huh-7-N cells, the EGFP specific siRNA was able to specifically inhibit the expression of EGFP in Huh-7-N. In comparison with that in wild-type Huh-7 or that in Huh-7 co-transfected with pEGFP-N1, the inhibition of EGFP specific siRNA in Huh-7-N cells is more significant and repeatable. It is concluded that a cell clone Huh-7-N, which stably expresses EGFP, has been established, and the in vitro synthesized EGFP siRNA can be used in silencing the EGFP gene expression. This Huh-7-N/EGFP specific siRNA system has been proved reliable and convenient, and can also be applied widely as control in other RNA interference studies. (C) 2003 Published by Elsevier B.V.
引用
收藏
页码:189 / 194
页数:6
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