Negative regulation of activation-induced cytidine deaminase in B cells

被引:72
|
作者
Muto, T
Okazaki, IM
Yamada, S
Tanaka, Y
Kinoshita, K
Muramatsu, M
Nagaoka, H
Honjo, T [1 ]
机构
[1] Kyoto Univ, Dept Immunol & Genom Med, Grad Sch Med, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, PRESTO, Japan Sci & Technol Corp, Sakyo Ku, Kyoto 6068501, Japan
[3] Kyoto Univ, Lab Immunol & Cell Biol, Grad Sch Biostudies, Sakyo Ku, Kyoto 6068501, Japan
[4] Akita Univ, Anim Res Lab, Biosci Res & Educ Ctr, Akita 0108543, Japan
关键词
antibodies; protein modification; transgenic/knockout mice;
D O I
10.1073/pnas.0510970103
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
Both class switch recombination (CSR) and somatic hypermutation (SHIM) of the Ig genes require the activity of activation-induced cytidine deaminase (AID). Expression of AID is restricted to B cells in the germinal centers of the lymphoid organs, where activated B cells undergo CSR and SHM. We previously showed that constitutive and systemic expression of AID leads to tumorigenesis in T cells and lung epithelium, but not in B cells. This finding led us to suspect that transgenic AID may be inactivated at least in part in B cells. To address this issue, we generated conditional AID-transgenic mice that constitutively express AID only in B cells. Studies on the cross between the AID-transgenic and AID-deficient mice showed that abundant AID protein accumulated by constitutive expression is inactivated in B cells, possibly providing an explanation for the absence of deregulation of CSR and SHM in AID-transgenic B cells.
引用
收藏
页码:2752 / 2757
页数:6
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