Small mitochondrial-targeted RNAs modulate endogenous mitochondrial protein expression in vivo

被引:9
|
作者
Towheed, Atif
Markantone, Desiree M.
Crain, Aaron T.
Celotto, Alicia M.
Palladino, Michael J. [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Chem Biol & Pharmacognosy, Pittsburgh, PA 15261 USA
基金
美国国家卫生研究院;
关键词
Mitochondrial disorders; Translation inhibitors; Non-coding small chimeric RNA; Mitochondrial encoded proteins; 5S RIBOSOMAL-RNA; DROSOPHILA-MELANOGASTER; ATP SYNTHASE; HUMAN-CELLS; IMPORT; DNA; SEQUENCE; GENE; MUTATION; MEMBRANE;
D O I
10.1016/j.nbd.2014.04.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Endogenous mitochondrial genes encode critical oxidative phosphorylation components and their mutation results in a set of disorders known collectively as mitochondrial encephalomyopathies. There is intensive interest in modulating mitochondrial function as organelle dysfunction has been associated with numerous disease states. Proteins encoded by the mitochondrial genome cannot be genetically manipulated by current techniques. Here we report the development of a mitochondrial-targeted RNA expression system (mtTRES) utilizing distinct non-coding leader sequences (NCLs) and enabling in vivo expression of small mitochondrial-targeted RNAs. mtTRES expressing small chimeric antisense RNAs was used as translational inhibitors (TLIs) to target endogenous mitochondrial protein expression in vivo. By utilizing chimeric antisense RNA we successfully modulate expression of two mitochondrially-encoded proteins, ATP6 and COXII, and demonstrate the utility of this system in vivo and in human cells. This technique has important and obvious research and clinical implications. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:15 / 22
页数:8
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