Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA.
| Autor: | Matumba TG; Centre for Ecological Genomics and Wildlife Conservation, Department of Zoology, University of Johannesburg, Auckland Park, 2006, South Africa.; Department of Zoology and Entomology, Rhodes University, Grahamstown, 6140, South Africa., Oliver J; Centre for Ecological Genomics and Wildlife Conservation, Department of Zoology, University of Johannesburg, Auckland Park, 2006, South Africa., Barker NP; Department of Plant and Soil Sciences, University of Pretoria, Hatfield, 0028, South Africa., McQuaid CD; Department of Zoology and Entomology, Rhodes University, Grahamstown, 6140, South Africa., Teske PR; Centre for Ecological Genomics and Wildlife Conservation, Department of Zoology, University of Johannesburg, Auckland Park, 2006, South Africa. |
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| Jazyk: | angličtina |
| Zdroj: | F1000Research [F1000Res] 2020 May 07; Vol. 9, pp. 339. Date of Electronic Publication: 2020 May 07 (Print Publication: 2020). |
| DOI: | 10.12688/f1000research.23635.1 |
| Abstrakt: | Background: Mitochondrial DNA (mtDNA) has long been used to date historical demographic events. The idea that it is useful for molecular dating rests on the premise that its evolution is neutral. Even though this idea has long been challenged, the evidence against clock-like evolution of mtDNA is often ignored. Here, we present a particularly clear and simple example to illustrate the implications of violations of the assumption of selective neutrality. Methods: DNA sequences were generated for the mtDNA COI gene and the nuclear 28S rRNA of two closely related rocky shore snails, and species-level variation was compared. To our knowledge, this is the first study to use nuclear rRNA at this taxonomic level, presumably because this marker is assumed to evolve so slowly that it is only suitable for phylogenetics. Results: Even though high inter-specific divergence reflected the faster evolutionary rate of COI, intraspecific genetic variation was similar for both markers. As a result, estimates of population expansion times based on mismatch distributions differed between the two markers by millions of years. Conclusions: Assuming that 28S evolves effectively clock-like, these findings can be explained by variation-reducing purifying selection in mtDNA at the species level, and an elevated divergence rate caused by diversifying selection between the two species. Although these two selective forces together make mtDNA suitable as a marker for species identifications by means of DNA barcoding because they create a 'barcoding gap', estimates of demographic change based on this marker can be expected to be highly unreliable. Our study contributes to the growing evidence that the utility of mtDNA sequence data beyond DNA barcoding is limited. Competing Interests: No competing interests were disclosed. (Copyright: © 2020 Matumba TG et al.) |
| Databáze: | MEDLINE |
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