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Multilineage transcriptional priming and determination of alternate hematopoietic cell fates.

来自 Elsevier

阅读量：

74

作者：

P Laslo，CJ Spooner，A Warmflash，DW Lancki，HJ Lee，R Sciammas，BN Gantner，AR Dinner，H Singh

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摘要：

Hematopoietic stem cells and their progenitors exhibit multilineage patterns of gene expression. Molecular mechanisms underlying the generation and refinement of these patterns during cell fate determination remain unexplored because of the absence of suitable experimental systems. Using PU.1 −/− progenitors, we demonstrate that at subthreshold levels, this Ets transcription factor regulates a mixed pattern (macrophage/neutrophil) of gene expression within individual myeloid progenitors. Increased PU.1 levels refine the pattern and promote macrophage differentiation by modulating a novel regulatory circuit comprised of counter antagonistic repressors, Egr-1,2/Nab-2 and Gfi-1. Egr-1 and Egr-2 function redundantly to activate macrophage genes and to repress the neutrophil program. These results are used to assemble and mathematically model a gene regulatory network that exhibits both graded and bistable behaviors and accounts for the onset and resolution of mixed lineage patterns during cell fate determination.

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关键词：

Animals Mice, Knockout Mice Macrophages Hematopoietic Stem Cells Transcription Factors Repressor Proteins RNA, Small Interfering DNA, Single-Stranded DNA-Binding Proteins

DOI：

10.1016/j.cell.2006.06.052

被引量：

1083

年份：

2006

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来源期刊

Cell
2006-01-11

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