Specific Inhibition of Transient and Stable EGFP Gene Expression by Double Stranded RNA Interference in Mouse Preimplantation Embryos

M. Hosoe, T. Furusawa, F. Inoue, M. Sakatani, T. Tokunaga, R. Schultz, Masashi Takahashi
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Abstract

Double stranded RNA (dsRNA) interference is a useful tool for interfering with gene function by promoting the sequence-dependent degradation of targeted mRNA in several organisms. In the present study, in order to confirm and improve the effect of dsRNA, we investigated an inhibitory effect of dsRNA on both transient and stable gene expression of enhanced green fluorescent protein (EGFP) in mouse preimplantation embryos. In the transient expression system, the rates of fluorescent embryos were significantly decreased by co-injection of EGFP dsRNA and EGFP expression vector fragment into the pronucleus of zygotes. In the stable expression system, EGFP expression in transgenic embryos was significantly decreased by injection of EGFP dsRNA into both the pronucleus and cytoplasm of zygotes, but, cytoplasmic injection caused a more significant EGFP inhibition than pronuclear injection. In quantitative PCR analysis, the expression of the EGFP gene was also inhibited by dsRNA injection, whereas the endogenous gene expression was not affected. These data suggest that dsRNA can inhibit the specific gene expression without affecting the development and expression of other genes.
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双链RNA干扰对小鼠着床前胚胎瞬时和稳定EGFP基因表达的特异性抑制
双链RNA (dsRNA)干扰是一种有用的工具,通过促进目标mRNA的序列依赖性降解来干扰基因功能。在本研究中,为了证实和提高dsRNA的作用,我们研究了dsRNA对小鼠着床前胚胎中增强型绿色荧光蛋白(EGFP)瞬时和稳定基因表达的抑制作用。在瞬时表达系统中,将EGFP dsRNA和EGFP表达载体片段共同注射到受精卵原核中,荧光胚胎率显著降低。在稳定表达系统中,将EGFP dsRNA注射到受精卵的原核和细胞质中,EGFP在转基因胚胎中的表达均显著降低,但细胞质注射对EGFP的抑制作用比原核注射更明显。在定量PCR分析中,注射dsRNA也抑制了EGFP基因的表达,而内源基因的表达不受影响。这些数据表明,dsRNA可以抑制特定基因的表达,而不影响其他基因的发育和表达。
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