Kim Sung-Ryul, Yang Jung-Il, Moon Sunok, Ryu Choong-Hwan, An Kyungsook, Kim Kyung-Me, Yim Jieun, An Gynheung
Department of Integrative Bioscience and Biotechnology, National Research Laboratory of Plant Functional Genomics and Functional Genomic Center, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Plant J. 2009 Sep;59(5):738-49. doi: 10.1111/j.1365-313X.2009.03909.x. Epub 2009 May 4.
RNA editing is the alteration of RNA sequences via insertion, deletion and conversion of nucleotides. In flowering plants, specific cytidine residues of RNA transcribed from organellar genomes are converted into uridines. Approximately 35 editing sites are present in the chloroplasts of higher plants; six pentatricopeptide repeat genes involved in RNA editing have been identified in Arabidopsis. However, although approximately 500 editing sites are found in mitochondrial RNAs of flowering plants, only one gene in Arabidopsis has been reported to be involved in such editing. Here, we identified rice mutants that are defective in seven specific RNA editing sites on five mitochondrial transcripts. Their various phenotypes include delayed seed germination, retarded growth, dwarfism and sterility. Mutant seeds from heterozygous plants are opaque. This mutation, named opaque and growth retardation 1 (ogr1), was generated by T-DNA insertion into a gene that encodes a pentatricopeptide repeat protein containing the DYW motif. The OGR1-sGFP fusion protein is localized to mitochondria. Ectopic expression of OGR1 in the mutant complements the altered phenotypes. We conclude that OGR1 is essential for RNA editing in rice mitochondria and is required for normal growth and development.
RNA编辑是指通过核苷酸的插入、缺失和转换来改变RNA序列。在开花植物中,从细胞器基因组转录而来的RNA的特定胞嘧啶残基会被转换为尿嘧啶。高等植物的叶绿体中大约存在35个编辑位点;在拟南芥中已鉴定出6个参与RNA编辑的五肽重复序列基因。然而,尽管在开花植物的线粒体RNA中发现了大约500个编辑位点,但在拟南芥中只有一个基因被报道参与这种编辑。在这里,我们鉴定了水稻突变体,这些突变体在五个线粒体转录本上的七个特定RNA编辑位点存在缺陷。它们的各种表型包括种子萌发延迟、生长迟缓、矮化和不育。来自杂合植物的突变种子是不透明的。这种突变被命名为不透明和生长迟缓1(ogr1),是由T-DNA插入到一个编码含有DYW基序的五肽重复序列蛋白的基因中产生的。OGR1-sGFP融合蛋白定位于线粒体。OGR1在突变体中的异位表达弥补了改变的表型。我们得出结论,OGR1对水稻线粒体中的RNA编辑至关重要,是正常生长和发育所必需的。