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Imaging Target mRNA and siRNA-Mediated Gene Silencing In Vivo with Ribozyme-Based Reporters
被引:14
|作者:
So, Min-Kyung
[1
,2
,3
]
Gowrishankar, Gayatri
[1
]
Hasegawa, Sumitaka
[1
]
Chung, June-Key
[2
,3
]
Rao, Jianghong
[1
]
机构:
[1] Stanford Univ, Sch Med, Canc Biol Programs, Dept Radiol,Mol Imaging Program Stanford, Stanford, CA 94305 USA
[2] Seoul Natl Univ, Coll Med, Dept Nucl Med, Lab Mol Imaging, Seoul 110744, South Korea
[3] Seoul Natl Univ, Coll Med, Therapy Canc Res Inst, Seoul 110744, South Korea
来源:
关键词:
imaging;
RNA reporter;
RNA;
siRNA;
trans-splicing ribozymes;
D O I:
10.1002/cbic.200800370
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Noninvasive imaging of specific mRNAs in living subjects promises numerous biological and medical applications. Common strategies use fluorescently or radioactively labelled antisense probes to detect target mRNAs through a hybridization mechanism, but have met with limited success in living animals. Here we present a novel molecular imaging approach based on the group I intron of Tetrahymena thermophila for imaging mRNA molecules in vivo. Engineered trans-splicing ribozyme reporters contain three domains, each of which is designed for targeting, splicing, and reporting. They can transduce the target mRNA into a reporter mRNA, leading to the production of reporter enzymes that can be noninvasively imaged in vivo. We have demonstrated this ribozyme-mediated RNA imaging method for imaging a mutant p53 mRNA both in single cells and noninvasively in living mice. After optimization, the ribozyme reporter increases contrast for the transiently expressed target by 180-fold, and by ten-fold for the stably expressed target. siRNA-mediated specific gene silencing of p53 expression has been successfully imaged in real time in vivo. This new ribozyme-based RNA reporter system should open up new avenues for in vivo RNA imaging and direct imaging of siRNA inhibition.
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页码:2682 / 2691
页数:10
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