Identifies candidate plastid genes involved in incompatibility in Campanula americana, suggesting new insights into evolution.
Most protein complexes within the chloroplast consist of both plastid and nuclear-encoded subunits. This integration leads to potential coevolution between the genomes, with disruption of coevolution a potential cause of plastid-nuclear incompatibility (PNI). Both plastid-nuclear coevolution and PNI have been found across many, sometimes overlapping, lineages of flowering plants. However, drawing a direct connection between these two phenomena has been difficult as the underlying genetics of PNI have been determined in only a handful of cases. The goal of this study was to identify candidate plastid genes contributing to the PNI observed in Campanula americana by analyzing patterns of evolution in plastid genes from the two most divergent lineages of C. americana as well as species across the Campanulaceae. Photosynthetic genes exhibited low rates of nucleotide substitution and dN/dS ratios indicating purifying selection, while several genes/gene families related to gene regulation and proteostasis ( rps , clpP1 , ycf2 ) exhibited elevated rates of nucleotide substitution and dN/dS ratios indicating relaxed or positive selection. The rps genes are the most likely candidates for contributing to the PNI in C. americana due to their high dN/dS ratios in both C. americana lineages and an increased rate of sequence evolution in C. americana and its close relatives. These results suggest that disruption of plastid translation could be a mechanism for intraspecific PNI in this species.
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Scoffield et al. (2026) studied this question.
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