Organelle trafficking of chimeric ribozymes and genetic manipulation of mitochondria

被引:22
作者
Val, Romain [1 ,2 ]
Wyszko, Eliza [3 ]
Valentin, Clarisse [1 ,2 ]
Szymanski, Maciej [3 ]
Cosset, Anne [1 ,2 ]
Alioua, Malek [1 ,2 ]
Dreher, Theo W. [4 ]
Barciszewski, Jan [3 ]
Dietrich, Andre [1 ,2 ]
机构
[1] CNRS, Inst Biol Mol Plantes, F-67084 Strasbourg, France
[2] Univ Strasbourg, F-67084 Strasbourg, France
[3] Polish Acad Sci, Inst Bioorgan Chem, PL-61704 Poznan, Poland
[4] Oregon State Univ, Dept Microbiol, Corvallis, OR 97331 USA
关键词
MOSAIC-VIRUS RNA; HAMMERHEAD RIBOZYMES; SELF-CLEAVAGE; LOW-MAGNESIUM; IN-VITRO; TRANSFORMATION; IMPORT; TRANSCRIPTION; IDENTIFICATION; CHLAMYDOMONAS;
D O I
10.1093/nar/gkr580
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
With the expansion of the RNA world, antisense strategies have become widespread to manipulate nuclear gene expression but organelle genetic systems have remained aside. The present work opens the field to mitochondria. We demonstrate that customized RNAs expressed from a nuclear transgene and driven by a transfer RNA-like (tRNA-like) moiety are taken up by mitochondria in plant cells. The process appears to follow the natural tRNA import specificity, suggesting that translocation indeed occurs through the regular tRNA uptake pathway. Upon validation of the strategy with a reporter sequence, we developed a chimeric catalytic RNA composed of a specially designed trans-cleaving hammerhead ribozyme and a tRNA mimic. Organelle import of the chimeric ribozyme and specific target cleavage within mitochondria were demonstrated in transgenic tobacco cell cultures and Arabidopsis thaliana plants, providing the first directed knockdown of a mitochondrial RNA in a multicellular eukaryote. Further observations point to mitochondrial messenger RNA control mechanisms related to the plant developmental stage and culture conditions. Transformation of mitochondria is only accessible in yeast and in the unicellular alga Chlamydomonas. Based on the widespread tRNA import pathway, our data thus make a breakthrough for direct investigation and manipulation of mitochondrial genetics.
引用
收藏
页码:9262 / 9274
页数:13
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