Activation-induced cytidine deaminase turns on somatic hypermutation in hybridomas

Alberto Martin, Philip D. Bardwell, Caroline J. Woo, Manxia Fan, Marc J. Shulman and Matthew D. Scharff ()
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Alberto Martin: Albert Einstein College of Medicine
Philip D. Bardwell: Albert Einstein College of Medicine
Caroline J. Woo: Albert Einstein College of Medicine
Manxia Fan: Albert Einstein College of Medicine
Marc J. Shulman: University of Toronto
Matthew D. Scharff: Albert Einstein College of Medicine

Nature, 2002, vol. 415, issue 6873, 802-806

Abstract: Abstract 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 centroblasts1, is required for this process, but its exact role is unknown2. 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.

Date: 2002
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DOI: 10.1038/nature714

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