ArticleAmerican journal of human genetics2001
Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees.
Article in American journal of human genetics, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.
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31 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Mutation rate estimates for 110 Y-chromosome STRs combining population and father-son pair data.European journal of human genetics : EJHG · 2011Pooled it
- Genealogical analysis as a new approach for the investigation of drug intolerance heritability.European journal of human genetics : EJHG · 2014Trial
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- Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population.Scientific reports · 2022Article
- Complete vertebrate mitogenomes reveal widespread repeats and gene duplications.Genome biology · 2021Article
- Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies.American journal of human genetics · 2018Article
- Different kinds of genetic markers permit inference of Paleolithic and Neolithic expansions in humans.European journal of human genetics : EJHG · 2017Article
- Maternal ancestry and population history from whole mitochondrial genomes.Investigative genetics · 2015Article
- Genetic isolation among the northwestern, southwestern and central-eastern Indian Ocean populations of the pronghorn spiny lobster Panulirus penicillatus.International journal of molecular sciences · 2014Article
- The history of the North African mitochondrial DNA haplogroup U6 gene flow into the African, Eurasian and American continents.BMC evolutionary biology · 2014Article
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- High mitochondrial mutation rates estimated from deep-rooting Costa Rican pedigrees.American journal of physical anthropology · 2012Article
- Control region variability of haplogroup C1d and the tempo of the peopling of the Americas.PloS one · 2011Article
- Mutation rate switch inside Eurasian mitochondrial haplogroups: impact of selection and consequences for dating settlement in Europe.PloS one · 2011Article
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- Frequency and pattern of heteroplasmy in the control region of human mitochondrial DNA.Journal of molecular evolution · 2008Article
- Mutation patterns of mtDNA: empirical inferences for the coding region.BMC evolutionary biology · 2008Article
- A Bayesian evaluation of human mitochondrial substitution rates.American journal of human genetics · 2008Article
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6 authors.
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Abstract
We studied mutations in the mtDNA control region (CR) using deep-rooting French-Canadian pedigrees. In 508 maternal transmissions, we observed four substitutions (0.0079 per generation per 673 bp, 95% CI 0.0023-0.186). Combined with other familial studies, our results add up to 18 substitutions in 1,729 transmissions (0.0104), confirming earlier findings of much greater mutation rates in families than those based on phylogenetic comparisons. Only 12 of these mutations occurred at independent sites, whereas three positions mutated twice each, suggesting that pedigree studies preferentially reveal a fraction of highly mutable sites. Fitting the data through use of a nonuniform rate model predicts the presence of 40 (95% CI 27-54) such fast sites in the whole CR, characterized by the mutation rate of 274 per site per million generations (95% CI 138-410). The corresponding values for hypervariable regions I (HVI; 1,729 transmissions) and II (HVII; 1,956 transmissions), are 19 and 22 fast sites, with rates of 224 and 274, respectively. Because of the high probability of recurrent mutations, such sites are expected to be of no or little informativity for the evaluation of mutational distances at the phylogenetic time scale. The analysis of substitution density in the alignment of 973 HVI and 650 HVII unrelated European sequences reveals that the bulk of the sites mutate at relatively moderate and slow rates. Assuming a star-like phylogeny and an average time depth of 250 generations, we estimate the rates for HVI and HVII at 23 and 24 for the moderate sites and 1.3 and 1.0 for the slow sites. The fast, moderate, and slow sites, at the ratio of 1:2:13, respectively, describe the mutation-rate heterogeneity in the CR. Our results reconcile the controversial rate estimates in the phylogenetic and familial studies; the fast sites prevail in the latter, whereas the slow and moderate sites dominate the phylogenetic-rate estimations.
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