<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Peters L</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pagination>e70507</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12420532</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>177(5)</volume><pubmed_abstract>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.</pubmed_abstract><journal>Physiologia plantarum</journal><pubmed_title>PPR596 Is Required for nad2 mRNA Splicing and Complex I Biogenesis in Mitochondria of Arabidopsis thaliana.</pubmed_title><pmcid>PMC12420532</pmcid><funding_grant_id>400681449/GRK2498</funding_grant_id><funding_grant_id>ME 4174/3‐1</funding_grant_id><funding_grant_id>ME 4174/3-1</funding_grant_id><pubmed_authors>Wagner VC</pubmed_authors><pubmed_authors>Schoeller T</pubmed_authors><pubmed_authors>Dwiani S</pubmed_authors><pubmed_authors>Kuhn K</pubmed_authors><pubmed_authors>Schallenberg-Rudinger M</pubmed_authors><pubmed_authors>Meyer EH</pubmed_authors><pubmed_authors>Peters L</pubmed_authors></additional><is_claimable>false</is_claimable><name>PPR596 Is Required for nad2 mRNA Splicing and Complex I Biogenesis in Mitochondria of Arabidopsis thaliana.</name><description>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.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep-Oct</publication><modification>2026-06-03T05:47:51.949Z</modification><creation>2026-04-25T03:14:56.527Z</creation></dates><accession>S-EPMC12420532</accession><cross_references><pubmed>40925877</pubmed><doi>10.1111/ppl.70507</doi></cross_references></HashMap>