Gualberto J M, Bonnard G, Lamattina L, Grienenberger J M
Institut de Biologie Moléculaire des Plantes du Centre National de la Recherche Scientifique, Université Louis Pasteur, Strasbourg, France.
Plant Cell. 1991 Oct;3(10):1109-20. doi: 10.1105/tpc.3.10.1109.
In plant mitochondria, RNA editing involves the conversion of cytidines in the genomic DNA into uridines in the corresponding RNA. Analysis of cDNAs prepared by reverse transcription of mitochondrial RNAs has shown that partially edited RNAs are present in wheat mitochondria. The extent of this partial editing as well as its potential influence on the corresponding protein sequence were studied along with the expression of a wheat mitochondrial locus. The sequence, expression, and RNA editing of the wheat mitochondrial transcription unit containing four open reading frames (nad3, rps12, orf299, orf156), all cotranscribed into a same predominant precursor RNA, have been studied. The product of orf156 is an 18-kD mitochondrial membrane protein of unknown function, whereas the product of orf299 could not be detected and this sequence seems to be a pseudogene. Sequences of cDNA clones derived by the polymerase chain reaction technique show that nad3, rps12, and orf156 transcripts are edited, whereas orf299 is not edited, except for a sequence identical to part of the coxII gene. Analysis of cDNA clones obtained from the precursor RNA shows the presence of a large number of partially edited nad3-rps12 transcripts with no evident polarity for the editing process. This shows that RNA editing is a post-transcriptional event. In addition, study of partial editing at the level of precursor, mature, and polysomal transcripts shows that mainly mature, completely edited sequences are used for translation. Deletions of a nucleotide at editing sites were observed in a number of cDNA clones, suggesting that C----U RNA editing in plant mitochondria would be achieved by nucleotide replacement.
在植物线粒体中,RNA编辑涉及将基因组DNA中的胞嘧啶转换为相应RNA中的尿嘧啶。对通过线粒体RNA逆转录制备的cDNA进行分析表明,小麦线粒体中存在部分编辑的RNA。研究了这种部分编辑的程度及其对相应蛋白质序列的潜在影响,同时研究了小麦线粒体基因座的表达。对包含四个开放阅读框(nad3、rps12、orf299、orf156)的小麦线粒体转录单元的序列、表达和RNA编辑进行了研究,所有这些开放阅读框都共同转录成一个相同的主要前体RNA。orf156的产物是一种功能未知的18-kD线粒体膜蛋白,而orf299的产物未被检测到,该序列似乎是一个假基因。通过聚合酶链反应技术获得的cDNA克隆序列表明,nad3、rps12和orf156转录本被编辑,而orf299未被编辑,除了一段与coxII基因部分相同的序列。对从前体RNA获得的cDNA克隆进行分析表明,存在大量部分编辑的nad3-rps12转录本,编辑过程没有明显的极性。这表明RNA编辑是一个转录后事件。此外,对前体、成熟和多核糖体转录本水平的部分编辑进行研究表明,主要是成熟的、完全编辑的序列用于翻译。在许多cDNA克隆中观察到编辑位点处的核苷酸缺失,这表明植物线粒体中的C→U RNA编辑是通过核苷酸替换实现的。