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
Lymphocyte Development Group, MRC Clinical Sciences Centre, Imperial College London, Du Cane Road, London W12 0NN, UK.
Immunity. 2007 Mar;26(3):335-44. doi: 10.1016/j.immuni.2007.02.010.
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 lambda5 in a stage-specific manner. In pre-BI cells, Ikaros modulated lambda5 expression in competition with the transcriptional activator EBF. This required Ikaros binding to the Igll1 (lambda5) promoter and was abolished either by mutation of the Ikaros DNA-binding domain or by deletion of a single Ikaros site from the Igll1 promoter. At the transition from the pre-BI to pre-BII stage, the expression of the Ikaros family member Aiolos was upregulated and required for the efficient silencing of Igll1. Aiolos expression was controlled by pre-BCR signals via the adaptor protein SLP-65. Thus, pre-BCR signaling regulates Aiolos and the silencing of Igll1 via a developmental-stage-specific feedback loop.
Ikaros DNA结合蛋白对淋巴细胞和其他造血谱系的发育至关重要,但它们如何与信号传导和转录的其他调节因子协同作用,以在发育过程中实现有序的基因表达仍不清楚。在这里,我们表明Ikaros蛋白以阶段特异性方式调节前B细胞受体成分lambda5。在pre-BI细胞中,Ikaros与转录激活因子EBF竞争调节lambda5的表达。这需要Ikaros与Igll1(lambda5)启动子结合,并且通过Ikaros DNA结合结构域的突变或从Igll1启动子中删除单个Ikaros位点而被消除。在从pre-BI到pre-BII阶段的转变过程中,Ikaros家族成员Aiolos的表达上调,并且是Igll1有效沉默所必需的。Aiolos的表达通过衔接蛋白SLP-65受前B细胞受体信号的控制。因此,前B细胞受体信号通过发育阶段特异性反馈环调节Aiolos和Igll1的沉默。