Nuclear compensatory evolution driven by mito-nuclear incompatibilities.

Proc Natl Acad Sci U S A

Departamento de Física da Matéria Condensada, Instituto de Física Gleb Wataghin, Universidade Estadual de Campinas (UNICAMP), Campinas 13083859, Brasil.

Published: October 2024

AI Article Synopsis

  • Mitochondrial function is influenced by both mitochondrial and nuclear gene expressions, showcasing resilience despite high mutation rates, which drives compensatory nuclear mutations for compatibility.
  • The study examines how mito-nuclear incompatibilities affect gene substitutions in species evolution, revealing that mating success relies on genetic compatibility and spatial proximity, while populations evolve from partially compatible states.
  • Findings suggest that selection for mito-nuclear compatibility varies in impact; it can reduce substitutions in compatible genes but promote compensation in incompatible ones, ultimately affecting rates of species radiation without directly correlating substitution rates to equilibrium richness.

Article Abstract

Mitochondrial function relies on the coordinated expression of mitochondrial and nuclear genes, exhibiting remarkable resilience despite high mitochondrial mutation rates. The nuclear compensation mechanism suggests deleterious mitochondrial alleles drive compensatory nuclear mutations to preserve mito-nuclear compatibility. However, prevalence and factors conditioning this phenomenon remain debated due to its conflicting evidence. Here, we investigate how mito-nuclear incompatibilities impact substitutions in a model for species radiation. Mating success depends on genetic compatibility (nuclear DNA) and spatial proximity. Populations evolve from partially compatible mito-nuclear states, simulating mitochondrial DNA (mtDNA) introgression. Mutations do not confer advantages nor disadvantages, but individual fecundity declines with increasing incompatibilities, selecting for mito-nuclear coordination. We find that selection for mito-nuclear compatibility affects each genome differently based on their initial state. In compatible gene pairs, selection reduces substitutions in both genomes, while in incompatible nuclear genes, it consistently promotes compensation, facilitated by more mismatches. Interestingly, high mitochondrial mutation rates can reduce nuclear compensation by increasing mtDNA rectification, while substitutions in initially compatible nuclear gene are boosted. Finally, the presence of incompatibilities accelerates species radiation, but equilibrium richness is not directly correlated to substitution rates, revealing the complex dynamics triggered by mitochondrial introgression and mito-nuclear coevolution. Our study provides a perspective on nuclear compensation and the role of mito-nuclear incompatibilities in speciation by exploring extreme scenarios and identifying trends that empirical data alone cannot reveal. We emphasize the challenges in detecting these dynamics and propose analyzing specific genomic signatures could shed light on this evolutionary process.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11494290PMC
http://dx.doi.org/10.1073/pnas.2411672121DOI Listing

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