Activation-induced cytidine deaminase turns on somatic hypermutation in hybridomas

被引:211
|
作者
Martin, A
Bardwell, PD
Woo, CJ
Fan, MX
Shulman, MJ
Scharff, MD
机构
[1] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10461 USA
[2] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature714
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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(1), is required for this process, but its exact role is unknown(2). 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.
引用
收藏
页码:802 / 806
页数:5
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