E-proteins directly regulate expression of activation-induced deaminase in mature B cells

被引:191
作者
Sayegh, CE [1 ]
Quong, MW [1 ]
Agata, Y [1 ]
Murre, C [1 ]
机构
[1] Univ Calif San Diego, Dept Biol Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ni923
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Activated mature B cells in which the DNA-binding activity of E-proteins has been disrupted fail to undergo class switch recombination. Here we show that activated B cells overexpressing the antagonist helix-loop-helix protein Id3 do not induce expression of the murine Aicda gene encoding activation-induced deaminase (AID). A highly conserved intronic regulatory element in Aicda binds E-proteins both in vitro and in vivo. The transcriptional activity of this element is regulated by E-proteins. We show that the enforced expression of AID in cells overexpressing Id3 partially restores class switch recombination. Taken together, our observations link helix-loop-helix activity and Aicda gene expression in a common pathway, in which E-protein activity is required for the efficient induction of Aicda transcription.
引用
收藏
页码:586 / 593
页数:8
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