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Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages
Resolving the absolute timescale of phylogenetic trees stipulates reliable estimates for the rate of DNA sequence evolution. For this end, various calibration methods have been developed and studied intensively. Intraspecific rate variation among distinct genetic lineages, however, has gained less a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250076/ https://www.ncbi.nlm.nih.gov/pubmed/35731946 http://dx.doi.org/10.1093/gbe/evac097 |
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author | Översti, Sanni Palo, Jukka U |
author_facet | Översti, Sanni Palo, Jukka U |
author_sort | Översti, Sanni |
collection | PubMed |
description | Resolving the absolute timescale of phylogenetic trees stipulates reliable estimates for the rate of DNA sequence evolution. For this end, various calibration methods have been developed and studied intensively. Intraspecific rate variation among distinct genetic lineages, however, has gained less attention. Here, we have assessed lineage-specific molecular rates of human mitochondrial DNA (mtDNA) by performing tip-calibrated Bayesian phylogenetic analyses. Tip-calibration, as opposed to traditional nodal time stamps from dated fossil evidence or geological events, is based on sample ages and becoming ever more feasible as ancient DNA data from radiocarbon-dated samples accumulate. We focus on subhaplogroups U2, U4, U5a, and U5b, the data including ancient mtDNA genomes from (14)C-dated samples (n = 234), contemporary genomes (n = 301), and two outgroup sequences from haplogroup R. The obtained molecular rates depended on the data sets (with or without contemporary sequences), suggesting time-dependency. More notable was the rate variation between haplogroups: U4 and U5a stand out having a substantially higher rate than U5b. This is also reflected in the divergence times obtained (U5a: 17,700 years and U5b: 29,700 years), a disparity not reported previously. After ruling out various alternative causes (e.g., selection, sampling, and sequence quality), we propose that the substitution rates have been influenced by demographic histories, widely different among populations where U4/U5a or U5b are frequent. As with the Y-chromosomal subhaplogroup R1b, the mitochondrial U4 and U5a have been associated with remarkable range extensions of the Yamnaya culture in the Bronze Age. |
format | Online Article Text |
id | pubmed-9250076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92500762022-07-05 Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages Översti, Sanni Palo, Jukka U Genome Biol Evol Research Article Resolving the absolute timescale of phylogenetic trees stipulates reliable estimates for the rate of DNA sequence evolution. For this end, various calibration methods have been developed and studied intensively. Intraspecific rate variation among distinct genetic lineages, however, has gained less attention. Here, we have assessed lineage-specific molecular rates of human mitochondrial DNA (mtDNA) by performing tip-calibrated Bayesian phylogenetic analyses. Tip-calibration, as opposed to traditional nodal time stamps from dated fossil evidence or geological events, is based on sample ages and becoming ever more feasible as ancient DNA data from radiocarbon-dated samples accumulate. We focus on subhaplogroups U2, U4, U5a, and U5b, the data including ancient mtDNA genomes from (14)C-dated samples (n = 234), contemporary genomes (n = 301), and two outgroup sequences from haplogroup R. The obtained molecular rates depended on the data sets (with or without contemporary sequences), suggesting time-dependency. More notable was the rate variation between haplogroups: U4 and U5a stand out having a substantially higher rate than U5b. This is also reflected in the divergence times obtained (U5a: 17,700 years and U5b: 29,700 years), a disparity not reported previously. After ruling out various alternative causes (e.g., selection, sampling, and sequence quality), we propose that the substitution rates have been influenced by demographic histories, widely different among populations where U4/U5a or U5b are frequent. As with the Y-chromosomal subhaplogroup R1b, the mitochondrial U4 and U5a have been associated with remarkable range extensions of the Yamnaya culture in the Bronze Age. Oxford University Press 2022-06-22 /pmc/articles/PMC9250076/ /pubmed/35731946 http://dx.doi.org/10.1093/gbe/evac097 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Översti, Sanni Palo, Jukka U Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages |
title | Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages |
title_full | Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages |
title_fullStr | Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages |
title_full_unstemmed | Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages |
title_short | Variation in the Substitution Rates among the Human Mitochondrial Haplogroup U Sublineages |
title_sort | variation in the substitution rates among the human mitochondrial haplogroup u sublineages |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250076/ https://www.ncbi.nlm.nih.gov/pubmed/35731946 http://dx.doi.org/10.1093/gbe/evac097 |
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