Abstract
We developed a method for rapid generation of B cell receptor (BCR) monoclonal mice expressing prerearranged Igh and Igk chains monoallelically from the Igh locus by CRISPR-Cas9 injection into fertilized oocytes. B cells from these mice undergo somatic hypermutation (SHM), class switch recombination (CSR), and affinity-based selection in germinal centers. This method combines the practicality of BCR transgenes with the ability to study Ig SHM, CSR, and affinity maturation.
© 2018 Jacobsen et al.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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B-Lymphocytes / cytology
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B-Lymphocytes / immunology*
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Germinal Center / cytology
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Germinal Center / immunology*
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Immunoglobulin Class Switching*
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Immunoglobulin Heavy Chains* / genetics
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Immunoglobulin Heavy Chains* / immunology
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Immunoglobulin kappa-Chains* / genetics
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Immunoglobulin kappa-Chains* / immunology
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Mice
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Mice, Transgenic
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Receptors, Antigen, B-Cell* / genetics
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Receptors, Antigen, B-Cell* / immunology
Substances
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Immunoglobulin Heavy Chains
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Immunoglobulin kappa-Chains
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Receptors, Antigen, B-Cell