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      The SCID but not the RAG-2 gene product is required for S mu-S epsilon heavy chain class switching.

      Immunity
      Animals, Antibodies, Monoclonal, diagnostic use, Antigens, CD40, physiology, B-Lymphocytes, cytology, Cell Differentiation, DNA-Binding Proteins, Gene Expression Regulation, Developmental, Genes, Immunoglobulin, Hybridomas, Immunoglobulin epsilon-Chains, genetics, Immunoglobulin mu-Chains, Immunophenotyping, Interleukin-4, pharmacology, Interleukin-7, Mice, Mice, Inbred C57BL, Mice, Inbred DBA, Mice, SCID, immunology, Proteins, Recombination, Genetic

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          Abstract

          We have investigated the capacity of precursor B cells from normal (BDF1) and V(D)J recombinase-deficient (RAG-27) or defective (SCID) mice to be induced by a CD40-specific monoclonal antibody and IL-4 to epsilon H chain gene transcription and to S mu-S epsilon switch recombination. In differentiating precursor B cells from all three strains of mice, the development of similar numbers of CD19+, CD23+, CD40+, and MHC class II+ expressing B lineage cells and similar levels of epsilon H chain gene transcription were induced. Efficient S mu-S epsilon switching occurred in normal and RAG-2-deficient, but not in SCID, precursor B cells. Thus, the transcription of the epsilon H chain is independent of the RAG-2 and the SCID gene product, while the S mu-S epsilon switch recombination requires the SCID gene-encoded DNA-dependent protein kinase, but not the RAG-2 protein.

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