Empty pericarp7 encodes a mitochondrial E‐subgroup pentatricopeptide repeat protein that is required for ccmFN editing, mitochondrial function and seed development in maize
2015
RNA editing, converting cytidines (C) to uridines (U) at specific sites in the transcripts of mitochondria and plastids, plays a critical role in organelle gene expression in land plants. Recently pentatricopeptide repeat (PPR) proteins were identified as site-specific recognition factors for RNA editing. In this study, we characterized an empty pericarp7 mutant (emp7) in Zea mays (maize), which confers an embryo-lethal phenotype. In emp7 mutants, mitochondrial functions are seriously perturbed, resulting in a strikingly reduced respiration rate. Emp7 encodes an E-subgroup PPR protein that is localized exclusively in the mitochondrion. Null mutation of Emp7 abolishes the CU editing of ccmF(N) transcript solely at position 1553. CcmF(N) is coding for a subunit of heme lyase complex in the cytochromec maturation pathway. The resulting PheSer substitution in CcmF(N) leads to the loss of CcmF(N) protein and a strikingly reduced c-type cytochrome. Consequently, the mitochondrial cytochrome-linked respiratory chain is impaired as a result of the disassembly of complexIII in the emp7 mutant. These results indicate that the PPR-E subgroup protein EMP7 is required for CU editing of ccmF(N)-1553 at a position essential for cytochromec maturation and mitochondrial oxidative phosphorylation, and hence is essential to embryo and endosperm development in maize.
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