Ikaros DNA-binding proteins as integral components of B cell developmental-stage-specific regulatory circuits

被引:157
作者
Thompson, Elizabeth C.
Cobb, Bradley S.
Sabbattini, Pierangela
Meixlsperger, Sonja
Parelho, Vania
Liberg, David
Taylor, Benjamin
Dillon, Niall
Georgopoulos, Katia
Jumaa, Hassan
Smale, Stephen T.
Fisher, Amanda G.
Merkenschlager, Matthias
机构
[1] Imperial Coll London, MRC, Ctr Clin Sci, Lymphocyte Dev Grp, London W12 0NN, England
[2] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
[4] Imperial Coll London, MRC, Ctr Clin Sci, Gene Regulat & Chromatin Grp, London W12 0NN, England
[5] Max Planck Inst Immunobiol, D-79108 Freiburg, Germany
[6] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Cutaneous Biol Res Ctr, Charlestown, MA 02129 USA
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.immuni.2007.02.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Ikaros DNA-binding proteins are critical for the development of lymphocytes and other hematopoietic lineages, but it remains unclear how they cooperate with other regulators of signaling and transcription to achieve ordered gene expression during development. Here, we show that Ikaros proteins regulate the pre-BCR component lambda 5 in a stage-specific manner. In pre-BI cells, Ikaros modulated lambda 5 expression in competition with the transcriptional activator EBF. This required Ikaros binding to the IgII1 (lambda 5) promoter and was abolished either by mutation of the Ikaros DNA-binding domain or by deletion of a single Ikaros site from the IgII1 promoter. At the transition from the pre-BI to pre-BI stage, the expression of the Ikaros family member Aiolos was upregulated and required for the efficient silencing of IgII1. Aiolos expression was controlled by pre-BCR signals via the adaptor protein SLP-65. Thus, pre-BCR signaling regulates Aiolos and the silencing of IgII1 via a developmental-stage-specific feedback loop.
引用
收藏
页码:335 / 344
页数:10
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