Transcriptional regulation of lymphocyte lineage commitment

被引:0
|
作者
Rothenberg, EV [1 ]
Telfer, JC
Anderson, MK
机构
[1] CALTECH, Div Biol, Pasadena, CA 91125 USA
[2] Stowers Inst Med Res, Kansas City, MO USA
关键词
D O I
10.1002/(SICI)1521-1878(199909)21:9<726::AID-BIES4>3.0.CO;2-S
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of T cells and B cells from pluripotent hematopoietic precursors occurs through a stepwise narrowing of developmental potential that ends in lineage commitment. During this process, lineage-specific genes are activated asynchronously, and lineage-inappropriate genes, although initially expressed, are asynchronously turned off. These complex gene expression-events are the outcome of the changes in expression of multiple transcription factors with partially overlapping roles in early lymphocyte and myeloid cell development. Key transcription factors promoting B-cell development and candidates for this role in T-cell development are discussed in terms of their possible modes of action in fate determination. We discuss how a robust, stable, cell-type-specific gene expression pattern may be established in part by the interplay between endogenous transcription factors and signals transduced by cytokine receptors, and in part by the network of effects of particular transcription factors on each other. (C) 1999 John Wiley & Sons, Inc.
引用
收藏
页码:726 / 742
页数:17
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