bioRxiv Science⌕ Search

Biology subjects

Raygoza, C. D.

Publications and source records attributed to Raygoza, C. D..

2 recordsLinked to original sources

A specialized SUV3 RNA helicase is involved in plant mitochondrial DNA repair

Synonymous substitution rates in the coding regions of land plant mitochondrial genomes are substantially lower than those in the nucleus. In contrast, non-coding regions are difficult or impossible to align except among very closely related species, suggesting that point mutation rates in these regions are considerably higher. Rearrangement breakpoints occur frequently within non-coding DNA, generating duplications, deletions, and inversions. To reconcile these contradictory patterns of genome evolution, it has been proposed that DNA damage is converted into double-strand breaks that are repaired through a combination of template-directed mechanisms and non-homologous end joining, while purifying selection preserves the integrity of coding sequences. Here we characterized AtSUV3, a mitochondrially targeted RNA helicase encoded by Arabidopsis thaliana At4g14790, a gene previously proposed to function as part of the plant mitochondrial degradosome. Mutations in AtSUV3 confer hypersensitivity to ciprofloxacin-induced mitochondrial DNA damage, CRISPR- knockout lines display increased ectopic recombination in the mitochondrial genome, and recombinant AtSUV3 exhibits ATP-dependent RNA helicase activity with a preference for 3'-ended substrates. Together, these findings identify AtSUV3 as a factor involved in mitochondrial dsDNA break repair. Consistent with our results, Arabidopsis and other plants encode an uncharacterized gene, AT5G39840.1, with 75% amino acid similarity with AtSUV3, dubbed herein as SUV3-like. We hypothesize that the AtSUV3 paralog has undergone specialization towards DNA repair, whereas AtSUV3-like protein may play a role in the plant organellar degradosome. Collectively, these findings identify AtSUV3 as a previously unrecognized factor involved in mitochondrial dsDNA break repair and provide a framework for understanding the diversification of DNA repair proteins during plant evolution.

plant biology↗

Plant Organellar Homologous Recombination Depends on Accessory Factors for Recombinase Activity

Plant mitochondrial and plastid genomes rely on homologous recombination (HR) for error-free DNA repair of double strand breaks. Here, we reconstructed the homologous recombination pathway of plant organelles from Arabidopsis, aiming to understand how proteins of diverse evolutionary origins assemble into a functional repair pathway. We found that the three bacterial-derived recombinases, AtRecAs assemble D-loop intermediates, but only chloroplast AtRecA1 independently execute end-joining recombination on large DNA substrates. AtRecA1-mediated end-joining recombination is enhanced by plant-unique single-stranded DNA-binding proteins of the Whirly and Organellar Single-Stranded Binding (OSB) families, in contrast these proteins are mandatory for the recombination activities of the dual-targeted AtRecA2 and mitochondrial AtRecA3. Recombinational intermediates generated by AtRecAs are resolved by a bacterial-like RadA helicase but not bacterial-like RecG. Finally, AtRecX inhibits the recombinase activities of AtRecA2, while the activities of AtRecA1 and AtRecA3 remains largely insensitive. Collectively, our results provide an integrative reconstitution of the plant organellar homologous recombination machinery, revealing that homologous recombination arises from a complex system of bacterial, phage-derived, plant-specific, and eukaryotic components. Plant-specific ssDNA-binding proteins emerge as key regulators of this process, promoting recombination efficiency and genome stability, that supports the essential functions of homologous recombination in DNA repair and DNA replication maintenance.

plant biology↗