Abstract
Mitochondrial genetic material (mtDNA) is widely used for phylogenetic reconstruction and as a barcode for species identification. The utility of mtDNA in these contexts derives from its particular molecular properties, including its high evolutionary rate, uniparental inheritance, and small size. But mtDNA may also play a fundamental role in speciation-as suggested by recent observations of coevolution with the nuclear DNA, along with the fact that respiration depends on coordination of genes from both sources. Here, we study how mito-nuclear interactions affect the accuracy of species identification by mtDNA, as well as the speciation process itself. We simulate the evolution of a population of individuals who carry a recombining nuclear genome and a mitochondrial genome inherited maternally. We compare a null model fitness landscape that lacks any mito-nuclear interaction against a scenario in which interactions influence fitness. Fitness is assigned to individuals according to their mito-nuclear compatibility, which drives the coevolution of the nuclear and mitochondrial genomes. Depending on the model parameters, the population breaks into distinct species and the model output then allows us to analyze the accuracy of mtDNA barcode for species identification. Remarkably, we find that species identification by mtDNA is equally accurate in the presence or absence of mito-nuclear coupling and that the success of the DNA barcode derives mainly from population geographical isolation during speciation. Nevertheless, selection imposed by mito-nuclear compatibility influences the diversification process and leaves signatures in the genetic content and spatial distribution of the populations, in three ways. First, speciation is delayed and the resulting phylogenetic trees are more balanced. Second, clades in the resulting phylogenetic tree correlate more strongly with the spatial distribution of species and clusters of more similar mtDNA's. Third, there is a substantial increase in the intraspecies mtDNA similarity, decreasing the number of alleles substitutions per locus and promoting the conservation of genetic information. We compare the evolutionary patterns observed in our model to empirical data from copepods (Tigriopus californicus). We find good qualitative agreement in the geographic patterns and the topology of the phylogenetic tree, provided the model includes selection based on mito-nuclear interactions. These results highlight the role of mito-nuclear compatibility in the speciation process and its reconstruction from genetic data.[Mito-nuclear coevolution; mtDNA barcode; parapatry; phylogeny.].
Highlights
Cellular respiration occurs in the mitochondrion, an organelle that differs from other cytoplasmic components in having its own genetic material, the mitochondrial DNA
Mito-nuclear interaction is simulated using a much simplified model of the complex process that takes place in the cell: we propose a phenomenological approach to quantify mito-nuclear compatibility based on the lock-and-key principle that guides the interaction between proteins coded by nuclear DNA (nDNA) and mitochondrial DNA (mtDNA) units
We establish an mtDNA-based classification to compare nDNA versus mtDNA barcode accuracy. Because no such criterion regarding reproductive isolation exists for the mitochondrial genome, in our model, we define an artificial mitochondrial genetic threshold GM : individuals are clustered according to their mitochondrial genetic distances and we identify a ‘species’ as a cluster of individuals whose distance to all others is larger than GM
Summary
Cellular respiration occurs in the mitochondrion, an organelle that differs from other cytoplasmic components in having its own genetic material, the mitochondrial DNA (mtDNA). In addition to their metabolic role in the production of energy, mitochondria play a key role in population genetics and evolutionary biology [1,2,3]. Due to its maternal inheritance, mtDNA is non-recombinant and free of the complications introduced by crossing over These properties, combined with its high evolutionary rate, make the mtDNA a powerful substrate for inferring the geographic structure of populations (e.g., [4]), hybridizations [5], and phylogenetic relationships [6]. The high rate of success to distinguish animal species motivates a more fundamental question: why does the barcode work and how does it relate to the nuclear DNA (nDNA) divergences during speciation?
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