Targeting the MicroRNA Passenger Strand for Regulating Therapeutic Transgenes

被引:3
|
作者
Kim, Sung Jin [1 ]
Lee, Chang Ho [1 ]
Lee, Seong-Wook [1 ]
机构
[1] Dankook Univ, Dept Mol Biol, Inst Nanosensor & Biotechnol, Res Inst Adv Omics, Yongin 448701, South Korea
基金
新加坡国家研究基金会;
关键词
ENDOGENOUS MICRORNA; VIRUS-REPLICATION; RNA ABUNDANCE; EXPRESSION; MIR-122; TISSUE; INHIBITORS; SPONGES; CELLS;
D O I
10.1089/nat.2015.0543
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
Gene therapy strategies have been developed, which can tissue or disease specifically regulate expression of exogenous transgenes by means of endogenous microRNA (miRNA) activity. However, the use of an endogenous guide strand to regulate an exogenous transgene could affect expression of endogenous miRNA target genes. In this study, we developed a new regulatory system of exogenous transgene expression by targeting the passenger strand. We constructed reporter constructs harboring miRNA-122 guide or passenger target sites with perfect or imperfect complementarity. We observed downregulation of an exogenous transgene harboring the miRNA-122 target sites against either the guide or passenger strand in cells expressing the cognate miRNA or cells stably expressing the miRNA target site. Moreover, the transgene activity as well as the gene expression level increased specifically by intracellular introduction of the antisense RNA against the corresponding strand. Endogenous target gene expression was induced by the transgene construct harboring the miRNA guide strand target sites, but not the passenger strand target sites. Importantly, the therapeutic transgene activity was efficiently regulated by targeting the passenger strand. These results suggested that an approach to passenger strand-regulated expression of therapeutic transgenes could be applied more safely as a therapeutic tool.
引用
收藏
页码:209 / 218
页数:10
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