| Literature DB >> 17363301 |
Elizabeth C Thompson1, Bradley S Cobb, Pierangela Sabbattini, Sonja Meixlsperger, Vania Parelho, David Liberg, Benjamin Taylor, Niall Dillon, Katia Georgopoulos, Hassan Jumaa, Stephen T Smale, Amanda G Fisher, Matthias Merkenschlager.
Abstract
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.Entities:
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Year: 2007 PMID: 17363301 DOI: 10.1016/j.immuni.2007.02.010
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745