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Transposable elements and introgression introduce genetic variation in the invasive ant Cardiocondyla obscurior

Zugehörigkeit
Institute for Evolution and Biodiversity, University of Münster, Münster, Germany
Errbii, Mohammed;
GND
1013858662
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Biosafety in Plant Biotechnology, Germany
Keilwagen, Jens;
Zugehörigkeit
Institute of Mathematics and Computer Science, University of Greifswald, Greifswald, Germany; Center for Functional Genomics of Microbes, University of Greifswald, Greifswald, Germany
Hoff, Katharina J.;
Zugehörigkeit
Institute for Evolution and Biodiversity, University of Münster, Münster, Germany
Steffen, Raphael;
GND
120823977
Zugehörigkeit
Cologne Center for Genomics, Institute of Human Genetics, University of Cologne, Cologne, Germany; Berlin Institute of Health at Charité –Universitätsmedizin Berlin, Core Facility Genomics, Berlin, Germany; Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany
Altmüller, Janine;
GND
136796362
Zugehörigkeit
Lehrstuhl für Zoologie/Evolutionsbiologie, University Regensburg, Regensburg, Germany
Oettler, Jan;
GND
1021190861
Zugehörigkeit
Institute for Evolution and Biodiversity, University of Münster, Münster, Germany
Schrader, Lukas

Introduced populations of invasive organisms have to cope with novel environmental challenges, while having reduced genetic variation caused by founder effects. The mechanisms associated with this “genetic paradox of invasive species” has received considerable attention, yet few studies have examined the genomic architecture of invasive species. Populations of the heart node ant Cardiocondyla obscurior belong to two distinct lineages, a New World lineage so far only found in Latin America and a more globally distributed Old World lineage. In the present study, we use population genomic approaches to compare populations of the two lineages with apparent divergent invasive potential. We find that the strong genetic differentiation of the two lineages began at least 40,000 generations ago and that activity of transposable elements (TEs) has contributed significantly to the divergence of both lineages, possibly linked to the very unusual genomic distribution of TEs in this species. Furthermore, we show that introgression from the Old World lineage is a dominant source of genetic diversity in the New World lineage, despite the lineages' strong genetic differentiation. Our study uncovers mechanisms underlying novel genetic variation in introduced populations of C. obscurior that could contribute to the species' adaptive potential.

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