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      AID is required for c-myc/IgH chromosome translocations in vivo.

      Cell
      Animals, B-Lymphocytes, metabolism, Cell Separation, Chromosomes, ultrastructure, Cytidine Deaminase, genetics, physiology, Enzyme-Linked Immunosorbent Assay, Flow Cytometry, Immunoglobulin G, chemistry, Immunoglobulins, Interleukin-6, Mice, Mice, Inbred BALB C, Mice, Transgenic, Models, Genetic, Polymerase Chain Reaction, Protein Transport, Proto-Oncogene Proteins c-myc, Time Factors, Translocation, Genetic

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          Abstract

          Chromosome translocations between c-myc and immunoglobulin (Ig) are associated with Burkitt's lymphoma in humans and with pristane- and IL6-induced plasmacytomas in mice. These translocations frequently involve Ig switch regions, suggesting that they might be the result of aberrant Ig class switch recombination (CSR). However, a direct link between CSR and chromosome translocations has not been established. We have examined c-myc/IgH translocations in IL6 transgenic mice that are mutant for activation induced cytidine deaminase (AID), the enzyme that initiates CSR. Here we report that AID is essential for the c-myc/IgH chromosome translocations induced by IL6.

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