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

Author:

Chamorro González Rocío,Conrad ThomasORCID,Stöber Maja C.ORCID,Xu RobinORCID,Giurgiu MădălinaORCID,Rodriguez-Fos Elias,Kasack Katharina,Brückner LotteORCID,van Leen EricORCID,Helmsauer KonstantinORCID,Dorado Garcia HeathcliffORCID,Stefanova Maria E.ORCID,Hung King L.ORCID,Bei YiORCID,Schmelz Karin,Lodrini Marco,Mundlos Stefan,Chang Howard Y.ORCID,Deubzer Hedwig E.ORCID,Sauer SaschaORCID,Eggert AngelikaORCID,Schulte Johannes H.ORCID,Schwarz Roland F.,Haase KerstinORCID,Koche Richard P.ORCID,Henssen Anton G.ORCID

Abstract

AbstractExtrachromosomal 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.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

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