TY - JOUR
T1 - RNAi in living mice.
AU - Hasuwa, Hidetoshi
AU - Okabe, Masaru
PY - 2004
Y1 - 2004
N2 - By introducing double-stranded RNAs (dsRNAs), it was shown that mRNAs that share sequences are destroyed, and that the translation step is severely downregulated (RNAi). This technique was demonstrated to be a very powerful tool for reverse genetics in Caenorhabditis elegans. However, studies have shown that RNAi can be achieved in living mice. In this chapter, we used "green mice" and "green rats" as model animals to demonstrate silencing of green fluorescent protein (GFP) expression by RNAi. In order to silence the gene, we produced transgenic mouse lines that produce dsRNA that is driven by the H1 promoter. It was demonstrated that the transgenically expressed, double stranded RNA could silence the GFP throughout the body of the mouse or rat and throughout the lifetime.
AB - By introducing double-stranded RNAs (dsRNAs), it was shown that mRNAs that share sequences are destroyed, and that the translation step is severely downregulated (RNAi). This technique was demonstrated to be a very powerful tool for reverse genetics in Caenorhabditis elegans. However, studies have shown that RNAi can be achieved in living mice. In this chapter, we used "green mice" and "green rats" as model animals to demonstrate silencing of green fluorescent protein (GFP) expression by RNAi. In order to silence the gene, we produced transgenic mouse lines that produce dsRNA that is driven by the H1 promoter. It was demonstrated that the transgenically expressed, double stranded RNA could silence the GFP throughout the body of the mouse or rat and throughout the lifetime.
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U2 - 10.1385/1-59259-746-7:501
DO - 10.1385/1-59259-746-7:501
M3 - Article
C2 - 15017075
AN - SCOPUS:2942711521
SN - 1064-3745
VL - 252
SP - 501
EP - 508
JO - Methods in molecular biology (Clifton, N.J.)
JF - Methods in molecular biology (Clifton, N.J.)
ER -