<scp>PPR596</scp> Is Required for <i>nad2</i> <scp>mRNA</scp> Splicing and Complex I Biogenesis in Mitochondria of <scp> <i>Arabidopsis thaliana</i> </scp>
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.
Authors
- Sarlita Dwiani
- Vera C. Wagner
- Mareike Schallenberg‐Rüdinger (ORCID: https://orcid.org/0000-0002-6874-4722)
- Etienne H. Meyer (ORCID: https://orcid.org/0000-0003-4712-9824)
- L. Peters (ORCID: https://orcid.org/0000-0002-1649-8582)
- Kristina Kuehn (ORCID: https://orcid.org/0000-0001-6747-783X)
- Theresa Schoeller
Institutions
- University of Bonn (DE)
- Martin Luther University Halle-Wittenberg (DE)
Publication Details
- Journal
- Physiologia Plantarum
- Published
- 2025-09-01
- DOI
- https://doi.org/10.1111/ppl.70507
- Citations
- 1
- Primary Topic
- RNA and protein synthesis mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- Deutsche Forschungsgemeinschaft