Institut Molekulare Botanik, Universität Ulm, D-89069, Ulm, Germany.
Plant J. 2013 May;74(4):593-604. doi: 10.1111/tpj.12143. Epub 2013 Apr 15.
The 5' ends of many mitochondrial transcripts are generated post-transcriptionally. Recently, we identified three RNA PROCESSING FACTORs required for 5' end maturation of different mitochondrial mRNAs in Arabidopsis thaliana. All of these factors are pentatricopeptide repeat proteins (PPRPs), highly similar to RESTORERs OF FERTILTY (RF), that rescue male fertility in cytoplasmic male-sterile lines from different species. Therefore, we suggested a general role of these RF-like PPRPs in mitochondrial 5' processing. We now identified RNA PROCESSING FACTOR 5, a PPRP not classified as an RF-like protein, required for the efficient 5' maturation of the nad6 and atp9 mRNAs as well as 26S rRNA. The precursor molecules of these RNAs share conserved sequence elements, approximately ranging from positions -50 to +9 relative to mature 5' mRNA termini, suggesting these sequences to be at least part of the cis elements required for processing. The knockout of RPF5 has only a moderate influence on 5' processing of atp9 mRNA, whereas the generation of the mature nad6 mRNA and 26S rRNA is almost completely abolished in the mutant. The latter leads to a 50% decrease of total 26S rRNA species, resulting in an imbalance between the large rRNA and 18S rRNA. Despite these severe changes in RNA levels and in the proportion between the 26S and 18S rRNAs, mitochondrial protein levels appear to be unaltered in the mutant, whereas seed germination capacity is markedly reduced.
许多线粒体转录物的 5' 端是在转录后产生的。最近,我们在拟南芥中鉴定出了三个 RNA 加工因子,它们是不同线粒体 mRNA 5' 成熟所必需的。所有这些因子都是五肽重复蛋白(PPRPs),与恢复育性的因子(RFs)高度相似,能够挽救来自不同物种的细胞质雄性不育系的雄性育性。因此,我们提出这些 RF 样 PPRPs 在线粒体 5' 加工中具有普遍作用。我们现在鉴定了 RNA 加工因子 5,它是一种不被归类为 RF 样蛋白的 PPRP,对于 nad6 和 atp9 mRNA 以及 26S rRNA 的有效 5' 成熟是必需的。这些 RNA 的前体分子共享保守的序列元件,大约在成熟 5' mRNA 末端的-50 到+9 位,表明这些序列至少是加工所需顺式元件的一部分。RPF5 的敲除对 atp9 mRNA 的 5' 加工只有适度的影响,而成熟 nad6 mRNA 和 26S rRNA 的产生在突变体中几乎完全被阻止。后者导致总 26S rRNA 种类减少 50%,导致大 rRNA 和 18S rRNA 之间的不平衡。尽管 RNA 水平和 26S 和 18S rRNA 之间的比例发生了这些严重变化,但突变体中线粒体蛋白水平似乎没有改变,而种子发芽能力明显降低。