B Lymphocyte Lineage Specification, Commitment and Epigenetic Control of Transcription by Early B Cell Factor 1

被引:41
|
作者
Hagman, James [1 ,2 ]
Ramirez, Julita [1 ,2 ]
Lukin, Kara [1 ,2 ]
机构
[1] Natl Jewish Hlth, Integrated Dept Immunol, Denver, CO 80206 USA
[2] Univ Colorado, Sch Med, Denver, CO 80206 USA
关键词
ANTIGEN RECEPTOR COMPLEX; FACTOR EBF; GENE-EXPRESSION; E2A PROTEINS; ACTIVATION DOMAINS; NONLYMPHOID CELLS; FATE COMMITMENT; FACTOR-BINDING; IL-7; RECEPTOR; MB-1; PROMOTER;
D O I
10.1007/82_2011_139
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Early B cell factor 1 (EBF1) is a transcription factor that is critical for both B lymphopoiesis and B cell function. EBF1 is a requisite component of the B lymphocyte transcriptional network and is essential for B lineage specification. Recent studies revealed roles for EBF1 in B cell commitment. EBF1 binds its target genes via a DNA-binding domain including a unique 'zinc knuckle', which mediates a novel mode of DNA recognition. Chromatin immunoprecipitation of EBF1 in pro-B cells defined hundreds of new, as well as previously identified, target genes. Notably, expression of the pre-B cell receptor (pre-BCR), BCR and PI3K/Akt/mTOR signaling pathways is controlled by EBF1. In this review, we highlight these current developments and explore how EBF1 functions as a tissue-specific regulator of chromatin structure at B cell-specific genes.
引用
收藏
页码:17 / 38
页数:22
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