So Min-Kyung, Gowrishankar Gayatri, Hasegawa Sumitaka, Chung June-Key, Rao Jianghong
Molecular Imaging Program at Stanford, Department of Radiology, Biophysics, Cancer Biology Programs, Stanford University School of Medicine, 1201 Welch Road, Stanford, California 94305-5484, USA.
Chembiochem. 2008 Nov 3;9(16):2682-91. doi: 10.1002/cbic.200800370.
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.
对活体动物体内特定信使核糖核酸(mRNA)进行无创成像有着众多生物学和医学应用前景。常见策略是使用荧光或放射性标记的反义探针,通过杂交机制检测目标mRNA,但在活体动物中的成效有限。在此,我们提出一种基于嗜热四膜虫I组内含子的新型分子成像方法,用于在体内对mRNA分子进行成像。工程化的反式剪接核酶报告基因包含三个结构域,每个结构域分别用于靶向、剪接和报告。它们能将目标mRNA转化为报告mRNA,从而产生可在体内进行无创成像的报告酶。我们已证明这种核酶介导的RNA成像方法可在单细胞中以及在活体小鼠体内无创地对突变型p53 mRNA进行成像。经过优化后,核酶报告基因使瞬时表达的目标对比度提高了180倍,使稳定表达的目标对比度提高了10倍。p53表达的小干扰RNA(siRNA)介导的特异性基因沉默已在体内成功实时成像。这种基于新核酶的RNA报告系统应为体内RNA成像和siRNA抑制的直接成像开辟新途径。