Circular DNA intermediates in the generation of large human segmental duplications

Springer Science and Business Media LLC - Tập 21 - Trang 1-11 - 2020
Javier U. Chicote1, Marcos López-Sánchez2,3, Tomàs Marquès-Bonet4,5,6, José Callizo7, Luis A. Pérez-Jurado2,3,8, Antonio García-España1
1Research Unit, Hospital Universitari de Tarragona Joan XXIII, Institut d’Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Tarragona, Spain
2Genetics Unit, Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, Barcelona, Spain
3Hospital del Mar Research Institute (IMIM) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain
4Institut de Biologia Evolutiva (CSIC-UPF), Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, Barcelona, Spain
5Catalan Institution of Research and Advanced Studies (ICREA), Barcelona, Spain
6CNAG-CRG, Centre for Genomic Regulation, Barcelona Institute of Science and Technology (BIST), Barcelona, Spain
7Department of Ophthalmology, Hospital Universitari de Tarragona Joan XXIII, Institut d’Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, Tarragona, Spain
8SA Clinical Genetics, Women’s and Children’s Hospital, South Australian Health and Medical Research Institute (SAHMRI) & University of Adelaide, Adelaide, Australia

Tóm tắt

Duplications of large genomic segments provide genetic diversity in genome evolution. Despite their importance, how these duplications are generated remains uncertain, particularly for distant duplicated genomic segments. Here we provide evidence of the participation of circular DNA intermediates in the single generation of some large human segmental duplications. A specific reversion of sequence order from A-B/C-D to B-A/D-C between duplicated segments and the presence of only microhomologies and short indels at the evolutionary breakpoints suggest a circularization of the donor ancestral locus and an accidental replicative interaction with the acceptor locus. This novel mechanism of random genomic mutation could explain several distant genomic duplications including some of the ones that took place during recent human evolution.

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