State Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Taian, 271018, China.
J Integr Plant Biol. 2020 Mar;62(3):299-313. doi: 10.1111/jipb.12843. Epub 2019 Sep 9.
Mitochondria, the main energy transducers in plant cells, require the proper assembly of respiratory chain complexes I-V for their function. The NADH dehydrogenase 4 (nad4) gene encodes mitochondrial respiratory chain complex I subunit IV, but the mechanism underlying nad4 transcript splicing is unclear. Here, we report that the P-type pentatricopeptide repeat (PPR) protein DEFECTIVE KERNEL 43 (DEK43) is responsible for cis-splicing of the nad4 transcript in maize. We demonstrate that DEK43 localizes to both the nucleus and mitochondria. The mutation of Dek43 resulted in embryo-lethal and light-colored defective kernels. Among the 22 mitochondrial group II introns, the splicing efficiency of nad4 introns 1 and 3 was reduced by up to 50% compared to the wild type. The levels of complex I and supercomplex I+III were also reduced in dek43. Furthermore, in-gel NADH dehydrogenase assays indicated that the activities of these complexes were significantly reduced in dek43. Further, the mitochondrial ultrastructure was altered in the mutant. Together, our findings indicate that DEK43, a dual-localized PPR protein, plays an important role in maintaining mitochondrial function and maize kernel development.
线粒体是植物细胞的主要能量转换器,其功能的正常发挥需要呼吸链复合物 I-V 的正确组装。NADH 脱氢酶 4(nad4)基因编码线粒体呼吸链复合物 I 的亚基 IV,但 nad4 转录本剪接的机制尚不清楚。在这里,我们报告 P 型五肽重复(PPR)蛋白 DEFECTIVE KERNEL 43(DEK43)负责玉米中 nad4 转录本的顺式剪接。我们证明 DEK43 定位于细胞核和线粒体。Dek43 的突变导致胚胎致死和浅色缺陷的核。在 22 种线粒体组 II 内含子中,nad4 内含子 1 和 3 的剪接效率与野生型相比降低了多达 50%。在 dek43 中,复合物 I 和超复合物 I+III 的水平也降低了。此外,凝胶内 NADH 脱氢酶测定表明这些复合物的活性在 dek43 中显著降低。此外,突变体中线粒体的超微结构发生了改变。总之,我们的研究结果表明,定位于核和线粒体的双重 PPR 蛋白 DEK43 在维持线粒体功能和玉米核发育中起着重要作用。