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Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells.
Chamorro González, Rocío; Conrad, Thomas; Stöber, Maja C; Xu, Robin; Giurgiu, Madalina; Rodriguez-Fos, Elias; Kasack, Katharina; Brückner, Lotte; van Leen, Eric; Helmsauer, Konstantin; Dorado Garcia, Heathcliff; Stefanova, Maria E; Hung, King L; Bei, Yi; Schmelz, Karin; Lodrini, Marco; Mundlos, Stefan; Chang, Howard Y; Deubzer, Hedwig E; Sauer, Sascha; Eggert, Angelika; Schulte, Johannes H; Schwarz, Roland F; Haase, Kerstin; Koche, Richard P; Henssen, Anton G.
Afiliación
  • Chamorro González R; Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Conrad T; Experimental and Clinical Research Center of the MDC and Charité Berlin, Berlin, Germany.
  • Stöber MC; Genomics Technology Platform, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
  • Xu R; Berlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
  • Giurgiu M; Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Rodriguez-Fos E; Faculty of Life Science, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Kasack K; Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Brückner L; Experimental and Clinical Research Center of the MDC and Charité Berlin, Berlin, Germany.
  • van Leen E; Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Helmsauer K; Experimental and Clinical Research Center of the MDC and Charité Berlin, Berlin, Germany.
  • Dorado Garcia H; Freie Universität Berlin, Berlin, Germany.
  • Stefanova ME; Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Hung KL; Experimental and Clinical Research Center of the MDC and Charité Berlin, Berlin, Germany.
  • Bei Y; Fraunhofer Institute for Cell Therapy and Immunology, Branch Bioanalytics and Bioprocesses IZI-BB, Potsdam, Germany.
  • Schmelz K; Experimental and Clinical Research Center of the MDC and Charité Berlin, Berlin, Germany.
  • Lodrini M; Max-Delbrück-Centrum für Molekulare Medizin, Berlin, Germany.
  • Mundlos S; Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Chang HY; Experimental and Clinical Research Center of the MDC and Charité Berlin, Berlin, Germany.
  • Deubzer HE; Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Sauer S; Experimental and Clinical Research Center of the MDC and Charité Berlin, Berlin, Germany.
  • Eggert A; Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Schulte JH; Experimental and Clinical Research Center of the MDC and Charité Berlin, Berlin, Germany.
  • Schwarz RF; RG Development and Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Haase K; Institute for Medical Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Koche RP; Center for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, CA, USA.
  • Henssen AG; Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Nat Genet ; 55(5): 880-890, 2023 05.
Article en En | MEDLINE | ID: mdl-37142849
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transcriptoma / Neoplasias Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transcriptoma / Neoplasias Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article País de afiliación: Alemania