| Literature DB >> 24509509 |
Tanja A Schwickert1, Hiromi Tagoh1, Sinan Gültekin2, Aleksandar Dakic1, Elin Axelsson2, Martina Minnich2, Anja Ebert2, Barbara Werner2, Mareike Roth2, Luisa Cimmino3, Ross A Dickins3, Johannes Zuber2, Markus Jaritz2, Meinrad Busslinger2.
Abstract
The transcription factor Ikaros is an essential regulator of lymphopoiesis. Here we studied its B cell-specific function by conditional inactivation of the gene encoding Ikaros (Ikzf1) in pro-B cells. B cell development was arrested at an aberrant 'pro-B cell' stage characterized by increased cell adhesion and loss of signaling via the pre-B cell signaling complex (pre-BCR). Ikaros activated genes encoding signal transducers of the pre-BCR and repressed genes involved in the downregulation of pre-BCR signaling and upregulation of the integrin signaling pathway. Unexpectedly, derepression of expression of the transcription factor Aiolos did not compensate for the loss of Ikaros in pro-B cells. Ikaros induced or suppressed active chromatin at regulatory elements of activated or repressed target genes. Notably, binding of Ikaros and expression of its target genes were dynamically regulated at distinct stages of early B lymphopoiesis.Entities:
Mesh:
Substances:
Year: 2014 PMID: 24509509 PMCID: PMC5790181 DOI: 10.1038/ni.2828
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606