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Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA

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 of...

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Autores principales: Matumba, Tshifhiwa G., Oliver, Jody, Barker, Nigel P., McQuaid, Christopher D., Teske, Peter R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7475959/
https://www.ncbi.nlm.nih.gov/pubmed/32934803
http://dx.doi.org/10.12688/f1000research.23635.2
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author Matumba, Tshifhiwa G.
Oliver, Jody
Barker, Nigel P.
McQuaid, Christopher D.
Teske, Peter R.
author_facet Matumba, Tshifhiwa G.
Oliver, Jody
Barker, Nigel P.
McQuaid, Christopher D.
Teske, Peter R.
author_sort Matumba, Tshifhiwa G.
collection PubMed
description 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. Nuclear rRNA is not usually used to study intraspecific variation in species that are not spatially structured, presumably because this marker is assumed to evolve so slowly that it is more 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 evolution is more 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.
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spelling pubmed-74759592020-09-14 Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA Matumba, Tshifhiwa G. Oliver, Jody Barker, Nigel P. McQuaid, Christopher D. Teske, Peter R. F1000Res Brief Report 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. Nuclear rRNA is not usually used to study intraspecific variation in species that are not spatially structured, presumably because this marker is assumed to evolve so slowly that it is more 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 evolution is more 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. F1000 Research Limited 2020-08-28 /pmc/articles/PMC7475959/ /pubmed/32934803 http://dx.doi.org/10.12688/f1000research.23635.2 Text en Copyright: © 2020 Matumba TG et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Matumba, Tshifhiwa G.
Oliver, Jody
Barker, Nigel P.
McQuaid, Christopher D.
Teske, Peter R.
Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA
title Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA
title_full Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA
title_fullStr Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA
title_full_unstemmed Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA
title_short Intraspecific mitochondrial gene variation can be as low as that of nuclear rRNA
title_sort intraspecific mitochondrial gene variation can be as low as that of nuclear rrna
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7475959/
https://www.ncbi.nlm.nih.gov/pubmed/32934803
http://dx.doi.org/10.12688/f1000research.23635.2
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