Number of the records: 1  

A revised timescale for human evolution based on ancient mitochondrial genomes

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    SYSNO ASEP0485576
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleA revised timescale for human evolution based on ancient mitochondrial genomes
    Author(s) Fu, Q. (CN)
    Mittnik, A. (DE)
    Johnson, P. L. F. (US)
    Bos, K. (DE)
    Lari, M. (IT)
    Bollongino, R. (DE)
    Sun, Ch. (CN)
    Giemsch, L. (DE)
    Schmitz, R. (DE)
    Burger, J. (DE)
    Ronchitelli, A. M. (IT)
    Martini, F. (IT)
    Cremonesi, R. G. (IT)
    Svoboda, Jiří (ARUB-Q) RID, ORCID, SAI
    Bauer, P. (DE)
    Caramelli, D. (IT)
    Castellano, S. (IT)
    Reich, D. (US)
    Pääbo, S. (DE)
    Krause, J. (DE)
    Source TitleCurrent Biology. - : Cell Press - ISSN 0960-9822
    Roč. 23, April 8 (2013), s. 553-559
    Number of pages7 s.
    Publication formPrint - P
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsmitochondrial genome ; human evolution ; calibration
    Subject RIVAC - Archeology, Anthropology, Ethnology
    OECD categoryArchaeology
    Institutional supportARUB-Q - RVO:68081758
    UT WOS000317371200018
    EID SCOPUS84876151646
    DOI10.1016/j.cub.2013.02.044
    AnnotationBackground: Recent analyses of de novo DNA mutations in modern humans have suggested a nuclear substitution rate that is approximately half that of previous estimates based on fossil calibration. This result has led to suggestions that major events in human evolution occurred far earlier than previously thought. Results: Here, we use mitochondrial genome sequences from ten securely dated ancient modern humans spanning 40,000 years as calibration points for the mitochondrial clock, thus yielding a direct estimate of the mitochondrial substitution rate. Our clock yields mitochondrial divergence times that are in agreement with earlier estimates based on calibration points derived from either fossils or archaeological material. In particular, our results imply a separation of non-Africans from the most closely related sub-Saharan African mitochondrial DNAs (haplogroup L3) that occurred less than 62-95 kya. Conclusions: Though single loci like mitochondrial DNA (mtDNA) can only provide biased estimates of population divergence times, they can provide valid upper bounds. Our results exclude most of the older dates for African and non-African population divergences recently suggested by de novo mutation rate estimates in the nuclear genome.
    WorkplaceInstitute of Archaeology (Brno)
    ContactHedvika Břínková, brinkova@arub.cz, Tel.: +420 515 911 112
    Year of Publishing2018
Number of the records: 1  

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