
doi: 10.1038/nature714
pmid: 11823785
The production of high-affinity protective antibodies requires somatic hypermutation (SHM) of the antibody variable (V)-region genes. SHM is characterized by a high frequency of point mutations that occur only during the centroblast stage of B-cell differentiation. Activation-induced cytidine deaminase (AID), which is expressed specifically in germinal-centre centroblasts, is required for this process, but its exact role is unknown. Here we show that AID is required for SHM in the centroblast-like Ramos cells, and that expression of AID is sufficient to induce SHM in hybridoma cells, which represent a later stage of B-cell differentiation that does not normally undergo SHM. In one hybridoma, mutations were exclusively in G*C base pairs that were mostly within RGYW or WRCY motifs, suggesting that AID has primary responsibility for mutations at these nucleotides. The activation of SHM in hybridomas indicates that AID does not require other centroblast-specific cofactors to induce SHM, suggesting either that it functions alone or that the factors it requires are expressed at other stages of B-cell differentiation.
B-Lymphocytes, AICDA (Activation-Induced Cytidine Deaminase), Hybridomas, Base Sequence, DNA Mutational Analysis, Molecular Sequence Data, Immunoglobulin Variable Region, Cell Differentiation, Lymphocyte Activation, Transfection, Cell Line, GC Rich Sequence, Codon, Nonsense, Cytidine Deaminase, Enzyme Induction, Humans, RNA, Messenger, Somatic Hypermutation, Immunoglobulin
B-Lymphocytes, AICDA (Activation-Induced Cytidine Deaminase), Hybridomas, Base Sequence, DNA Mutational Analysis, Molecular Sequence Data, Immunoglobulin Variable Region, Cell Differentiation, Lymphocyte Activation, Transfection, Cell Line, GC Rich Sequence, Codon, Nonsense, Cytidine Deaminase, Enzyme Induction, Humans, RNA, Messenger, Somatic Hypermutation, Immunoglobulin
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