Peters Leonora, Wagner Vera C, Schoeller Theresa, Dwiani Sarlita, Schallenberg-Rüdinger Mareike, Meyer Etienne H, Kühn Kristina
Department of Plant Physiology, Institute of Biology, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Germany.
Institut für Zelluläre Und Molekulare Botanik, Abteilung Molekulare Evolution, Universität Bonn, Bonn, Germany.
Physiol Plant. 2025 Sep-Oct;177(5):e70507. doi: 10.1111/ppl.70507.
Several genes in the mitochondria of angiosperms are interrupted by introns, and their posttranscriptional excision involves numerous nucleus-encoded auxiliary factors. Most of these factors are of eukaryotic origin, among them members of the pentatricopeptide-repeat (PPR) family of RNA-binding proteins. This family divides into the PLS and P classes, with PLS-class proteins typically participating in C-to-U mRNA editing and P-class members contributing to transcript stabilization and intron splicing. The P-class protein PPR596 was previously described to be involved in mitochondrial RNA editing, with the ppr596 mutant showing moderately elevated editing of a specific, partially edited site within the rps3 mRNA. PPR596 disruption led to a substantial delay in plant development. Because the moderate change in RNA editing in the ppr596 mutant is unlikely to be the cause of its severe developmental retardation, we re-investigated mitochondrial gene expression and found that PPR596 is specifically required for the efficient excision of the third intron from the nad2 pre-mRNA. Insufficient splicing of this intron in ppr596 impairs respiratory-chain complex I biogenesis at the step of the insertion of the Nad2 subunit, thus perturbing plant development.
被子植物线粒体中的几个基因被内含子打断,其转录后切除涉及众多细胞核编码的辅助因子。这些因子大多起源于真核生物,其中包括RNA结合蛋白五肽重复序列(PPR)家族的成员。该家族分为PLS类和P类,PLS类蛋白通常参与C-to-U mRNA编辑,P类成员则有助于转录本稳定和内含子剪接。先前已描述P类蛋白PPR596参与线粒体RNA编辑,ppr596突变体在rps3 mRNA内一个特定的、部分编辑的位点显示出适度升高的编辑水平。PPR596的破坏导致植物发育显著延迟。由于ppr596突变体中RNA编辑的适度变化不太可能是其严重发育迟缓的原因,我们重新研究了线粒体基因表达,发现PPR596是nad2前体mRNA有效切除第三个内含子所特需的。ppr596中该内含子剪接不足会在Nad2亚基插入步骤损害呼吸链复合体I的生物合成,从而扰乱植物发育。