五三肽重复
RNA剪接
内含子
生物
RNA结合蛋白
SR蛋白
遗传学
第二组内含子
细胞生物学
外显子剪接增强剂
线粒体
基因
RNA编辑
线粒体DNA
剪接体
核糖核酸
作者
Kaijian Fan,Zhenjing Ren,Xiaofeng Zhang,Yan Liu,Junjie Fu,Chunlai Qi,Wurinile Tatar,Allan G. Rasmusson,Guoying Wang,Yunjun Liu
摘要
Abstract Intron splicing is an essential event in post-transcriptional RNA processing in plant mitochondria, which requires the participation of diverse nuclear-encoded splicing factors. However, it is presently unclear how these proteins cooperatively take part in the splicing of specific introns. In this study, we characterized a nuclear-encoded mitochondrial P-type pentatricopeptide repeat (PPR) protein named EMP603. This protein is essential for splicing of intron 2 in the Nad1 gene and interacts with the mitochondria-localized DEAD-box RNA helicase PMH2-5140, the RAD52-like proteins ODB1-0814 and ODB1-5061, and the CRM domain-containing protein Zm-mCSF1. Further study revealed that the N-terminal region of EMP603 interacts with the DEAD-box of PMH2-5140, the CRM domain of Zm-mCSF1, and OBD1-5061, but not with OBD1-0814, whereas the PPR domain of EMP603 can interact with ODB1-0814, ODB1-5061, and PMH2-5140, but not with Zm-mCSF1. Defects in EMP603 severely disrupt the assembly and activity of mitochondrial complex I, leading to impaired mitochondrial function, and delayed seed development. The interactions revealed between EMP603 and PMH2-5140, ODB1-0814, ODB1-5061, and Zm-mCSF1 indicate a possible involvement of a dynamic ‘spliceosome-like’ complex in intron splicing, and may accelerate the elucidation of the intron splicing mechanism in plant mitochondria.
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