[HTML][HTML] Unrepaired DNA breaks in p53-deficient cells lead to oncogenic gene amplification subsequent to translocations

C Zhu, KD Mills, DO Ferguson, C Lee, J Manis… - Cell, 2002 - cell.com
C Zhu, KD Mills, DO Ferguson, C Lee, J Manis, J Fleming, Y Gao, CC Morton, FW Alt
Cell, 2002cell.com
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 …
Abstract
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.
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