Substitutions of short heterologous DNA segments of intragenomic or extragenomic origins produce clustered genomic polymorphisms

In a screen for unexplained mutation events we identified a previously unrecognized mechanism generating clustered DNA polymorphisms such as microindels and cumulative SNPs. The mechanism, short-patch double illegitimate recombination (SPDIR), facilitates short single-stranded DNA molecules to invad...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2016-12, Vol.113 (52), p.15066-15071
Hauptverfasser: Harms, Klaus, Lunnan, Asbjørn, Hülter, Nils, Mourier, Tobias, Vinner, Lasse, Andam, Cheryl P., Marttinen, Pekka, Fridholm, Helena, Hansen, Anders Johannes, Hanage, William P., Nielsen, Kaare Magne, Willerslev, Eske, Johnsen, Pål Jarle
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Sprache:eng
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Zusammenfassung:In a screen for unexplained mutation events we identified a previously unrecognized mechanism generating clustered DNA polymorphisms such as microindels and cumulative SNPs. The mechanism, short-patch double illegitimate recombination (SPDIR), facilitates short single-stranded DNA molecules to invade and replace genomic DNA through two joint illegitimate recombination events. SPDIR is controlled by key components of the cellular genome maintenance machinery in the gram-negative bacterium Acinetobacter baylyi. The source DNA is primarily intragenomic but can also be acquired through horizontal gene transfer. The DNA replacements are nonreciprocal and locus independent. Bioinformatic approaches reveal occurrence of SPDIR events in the gram-positive human pathogen Streptococcus pneumoniae and in the human genome.
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.1615819114