The transcriptional regulation of B cell lineage commitment

被引:285
作者
Nutt, Stephen L.
Kee, Barbara L.
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[2] Univ Chicago, Dept Pathol, Committee Immunol, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Pathol, Committee Canc Biol, Chicago, IL 60637 USA
[4] Univ Chicago, Dept Pathol, Committee Dev Biol, Chicago, IL 60637 USA
关键词
D O I
10.1016/j.immuni.2007.05.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The expression of lineage-associated genes, as well as the survival and expansion of committed B cell progenitors, is controlled by multiple transcriptional regulators and growth-factor receptors. Whereas certain DNA-binding proteins, such as lkaros and PU.1, are required primarily for the formation of more primitive lymphoid progenitors, other factors such as E2A and EBF1 have more direct roles in specifying the B cell-specific gene-expression program. Further, Pax5 functions to promote B cell commitment by repressing lineage-inappropriate gene expression and reinforcing B cell-specific gene expression. In this review, we focus on recent studies that have revealed that instead of a simple transcriptional hierarchy, efficient B cell commitment and differentiation requires the combinatorial activity of multiple transcription factors in a complex gene regulatory network.
引用
收藏
页码:715 / 725
页数:11
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