Abstract
The Eμ-Myc mouse is an extensively used model of MYC driven malignancy; however to date there has only been partial characterization of MYC co-operative mutations leading to spontaneous lymphomagenesis. Here we sequence spontaneously arising Eμ-Myc lymphomas to define transgene architecture, somatic mutations, and structural alterations. We identify frequent disruptive mutations in the PRC1-like component and BCL6-corepressor gene Bcor. Moreover, we find unexpected concomitant multigenic lesions involving Cdkn2a loss and other cancer genes including Nras, Kras and Bcor. These findings challenge the assumed two-hit model of Eμ-Myc lymphoma and demonstrate a functional in vivo role for Bcor in suppressing tumorigenesis.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alleles
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Animals
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B-Lymphocytes / immunology
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B-Lymphocytes / metabolism*
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B-Lymphocytes / pathology
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CRISPR-Cas Systems
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Cyclin-Dependent Kinase Inhibitor p16 / genetics
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Cyclin-Dependent Kinase Inhibitor p16 / immunology
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Disease Models, Animal
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Gene Editing
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Gene Expression Regulation, Neoplastic*
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Gene Frequency
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Janus Kinase 2 / genetics
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Janus Kinase 2 / immunology
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Lymphoma, B-Cell / genetics*
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Lymphoma, B-Cell / immunology
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Lymphoma, B-Cell / pathology
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Mice
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Mice, Transgenic
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Mutation*
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Proto-Oncogene Proteins c-myc / genetics*
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Proto-Oncogene Proteins c-myc / immunology
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Proto-Oncogene Proteins p21(ras) / genetics
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Proto-Oncogene Proteins p21(ras) / immunology
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Repressor Proteins / genetics*
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Repressor Proteins / immunology
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STAT5 Transcription Factor / genetics
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STAT5 Transcription Factor / immunology
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Transcriptome
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Tumor Suppressor Protein p53 / genetics
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Tumor Suppressor Protein p53 / immunology
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Whole Genome Sequencing
Substances
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Bcor protein, mouse
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Cdkn2a protein, mouse
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Cyclin-Dependent Kinase Inhibitor p16
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Myc protein, mouse
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Proto-Oncogene Proteins c-myc
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Repressor Proteins
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STAT5 Transcription Factor
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Trp53 protein, mouse
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Tumor Suppressor Protein p53
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Jak2 protein, mouse
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Janus Kinase 2
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Hras protein, mouse
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Proto-Oncogene Proteins p21(ras)