Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Sciences, Shandong University, Qingdao 266237, China.
College of Life Science, Yangtze University, Jingzhou 434025, China.
Plant Physiol. 2022 Oct 27;190(3):1763-1776. doi: 10.1093/plphys/kiac379.
Splicing of plant mitochondrial introns is facilitated by numerous nucleus-encoded protein factors. Although some splicing factors have been identified in plants, the mechanism underlying mitochondrial intron splicing remains largely unclear. In this study, we identified a small P-type pentatricopeptide repeat (PPR) protein containing merely four PPR repeats, small PPR protein 2 (SPR2), which is required for the splicing of more than half of the introns in maize (Zea mays) mitochondria. Null mutations of Spr2 severely impair the splicing of 15 out of the 22 mitochondrial Group II introns, resulting in substantially decreased mature transcripts, which abolished the assembly and activity of mitochondrial complex I. Consequently, embryogenesis and endosperm development were arrested in the spr2 mutants. Yeast two-hybrid, luciferase complementation imaging, bimolecular fluorescence complementation, and semi-in vivo pull-down analyses indicated that SPR2 interacts with small MutS-related domain protein PPR-SMR1, both of which are required for the splicing of 13 introns. In addition, SPR2 and/or PPR-SMR1 interact with other splicing factors, including PPR proteins EMPTY PERICARP16, PPR14, and chloroplast RNA splicing and ribosome maturation (CRM) protein Zm-mCSF1, which participate in the splicing of specific intron(s) of the 13 introns. These results prompt us to propose that SPR2/PPR-SMR1 serves as the core component of a splicing complex and possibly exerts the splicing function through a dynamic interaction with specific substrate recognizing PPR proteins in mitochondria.
植物线粒体内含子的剪接由许多核编码蛋白因子促进。虽然已经在植物中鉴定出一些剪接因子,但线粒体内含子剪接的机制在很大程度上仍不清楚。在这项研究中,我们鉴定了一个仅含有四个 PPR 重复序列的小 P 型五肽重复(PPR)蛋白,即小 PPR 蛋白 2(SPR2),它是玉米(Zea mays)线粒体中超过一半内含子剪接所必需的。Spr2 的缺失突变严重损害了 22 个线粒体组 II 内含子中的 15 个的剪接,导致成熟转录本显著减少,从而破坏了线粒体复合物 I 的组装和活性。因此,spr2 突变体中的胚胎发生和胚乳发育被阻断。酵母双杂交、荧光素酶互补成像、双分子荧光互补和半体内下拉分析表明,SPR2 与小 MutS 相关结构域蛋白 PPR-SMR1 相互作用,两者都是 13 个内含子剪接所必需的。此外,SPR2 和/或 PPR-SMR1 与其他剪接因子相互作用,包括 PPR 蛋白 EMPTY PERICARP16、PPR14 和叶绿体 RNA 剪接和核糖体成熟(CRM)蛋白 Zm-mCSF1,它们参与了 13 个内含子中的特定内含子的剪接。这些结果促使我们提出 SPR2/PPR-SMR1 作为剪接复合物的核心组成部分,并可能通过与线粒体中特定的底物识别 PPR 蛋白的动态相互作用发挥剪接功能。