Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells

Rocío Chamorro González(Humboldt-Universität zu Berlin), Thomas Conrad(Max Delbrück Center), Maja C Stöber(Max Delbrück Center), Robin Xu(Humboldt-Universität zu Berlin), Mădălina Giurgiu(Humboldt-Universität zu Berlin), Elias Rodríguez-Fos(Humboldt-Universität zu Berlin), Katharina Kasack(Fraunhofer Institute for Cell Therapy and Immunology), Lotte Brückner(Max Delbrück Center), Eric van Leen(Humboldt-Universität zu Berlin), Konstantin Helmsauer(Humboldt-Universität zu Berlin), Heathcliff Dorado García(Humboldt-Universität zu Berlin), Maria E. Stefanova(Max Planck Institute for Molecular Genetics), King L. Hung(Stanford University), Yi Bei(Humboldt-Universität zu Berlin), Karin Schmelz(Humboldt-Universität zu Berlin), Marco Lodrini(Humboldt-Universität zu Berlin), Stefan Mundlos(Max Planck Institute for Molecular Genetics), Howard Y. Chang(Howard Hughes Medical Institute), Hedwig E. Deubzer(German Cancer Research Center), Sascha Sauer(Max Delbrück Center), Angelika Eggert(German Cancer Research Center), Johannes H. Schulte(German Cancer Research Center), Roland F. Schwarz(University of Cologne), Kerstin Haase(German Cancer Research Center), Richard P. Koche(Memorial Sloan Kettering Cancer Center), Anton G. Henssen(German Cancer Research Center)
Nature Genetics
May 1, 2023
Cited by 81Open Access
Full Text

Abstract

Extrachromosomal DNAs (ecDNAs) are common in cancer, but many questions about their origin, structural dynamics and impact on intratumor heterogeneity are still unresolved. Here we describe single-cell extrachromosomal circular DNA and transcriptome sequencing (scEC&T-seq), a method for parallel sequencing of circular DNAs and full-length mRNA from single cells. By applying scEC&T-seq to cancer cells, we describe intercellular differences in ecDNA content while investigating their structural heterogeneity and transcriptional impact. Oncogene-containing ecDNAs were clonally present in cancer cells and drove intercellular oncogene expression differences. In contrast, other small circular DNAs were exclusive to individual cells, indicating differences in their selection and propagation. Intercellular differences in ecDNA structure pointed to circular recombination as a mechanism of ecDNA evolution. These results demonstrate scEC&T-seq as an approach to systematically characterize both small and large circular DNA in cancer cells, which will facilitate the analysis of these DNA elements in cancer and beyond.


Related Papers

No related papers found

Powered by citation graph analysis