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http://purl.uniprot.org/citations/12110179http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/12110179http://www.w3.org/2000/01/rdf-schema#comment"Amplification of large genomic regions associated with complex translocations (complicons) is a basis for tumor progression and drug resistance. We show that pro-B lymphomas in mice deficient for both p53 and nonhomologous end-joining (NHEJ) contain complicons that coamplify c-myc (chromosome 15) and IgH (chromosome 12) sequences. While all carry a translocated (12;15) chromosome, coamplified sequences are located within a separate complicon that often involves a third chromosome. Complicon formation is initiated by recombination of RAG1/2-catalyzed IgH locus double-strand breaks with sequences downstream of c-myc, generating a dicentric (15;12) chromosome as an amplification intermediate. This recombination event employs a microhomology-based end-joining repair pathway, as opposed to classic NHEJ or homologous recombination. These findings suggest a general model for oncogenic complicon formation."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.org/dc/terms/identifier"doi:10.1016/s0092-8674(02)00770-5"xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Gao Y."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Lee C."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Morton C.C."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Zhu C."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Fleming J."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Alt F.W."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Ferguson D.O."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Manis J."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/author"Mills K.D."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/name"Cell"xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/pages"811-821"xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/title"Unrepaired DNA breaks in p53-deficient cells lead to oncogenic gene amplification subsequent to translocations."xsd:string
http://purl.uniprot.org/citations/12110179http://purl.uniprot.org/core/volume"109"xsd:string
http://purl.uniprot.org/citations/12110179http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/12110179
http://purl.uniprot.org/citations/12110179http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/12110179
http://purl.uniprot.org/uniprot/#_E0CY05-mappedCitation-12110179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12110179
http://purl.uniprot.org/uniprot/#_E0CZC8-mappedCitation-12110179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12110179
http://purl.uniprot.org/uniprot/#_E0CZD1-mappedCitation-12110179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12110179
http://purl.uniprot.org/uniprot/#_A0A0R4J024-mappedCitation-12110179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12110179
http://purl.uniprot.org/uniprot/#_A0A0R4J1Y0-mappedCitation-12110179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12110179
http://purl.uniprot.org/uniprot/#_A6YM30-mappedCitation-12110179http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/12110179