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Genome-wide Lineage-Specific Transcriptional Networks Underscore Ikaros-Dependent Lymphoid Priming in Hematopoietic Stem Cells

机译:全基因组谱系特异性转录网络推断造血干细胞中Ikaros依赖性淋巴引发

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摘要

The mechanisms regulating lineage potential during early hematopoiesis were investigated. First, a cascade of lineage-affiliated gene expression signatures, primed in hematopoietic stem cells (HSCs) and differentially propagated in lineage-restricted progenitors, was identified. Lymphoid transcripts were primed as early as the HSC, together with myeloid and erythroid transcripts. Although this multilineage priming was resolved upon subsequent lineage restrictions, an unexpected cosegregation of lymphoid and myeloid gene expression and potential past a nominal myeloid restriction point was identified. Finally, we demonstrated that whereas the zinc finger DNA-binding factor Ikaros was required for induction of lymphoid lineage priming in the HSC, it was also necessary for repression of genetic programs compatible with self-renewal and multipotency downstream of the HSC. Taken together, our studies provide new insight into the priming and restriction of lineage potentials during early hematopoiesis and identify Ikaros as a key bivalent regulator of this process. © 2009 Elsevier Inc. All rights reserved.
机译:研究了早期造血过程中调节谱系潜能的机制。首先,鉴定了由血统干细胞(HSC)引发并在血统受限祖细胞中差异繁殖的一系列血统相关基因表达签名。最早在HSC上启动了淋巴样转录物,以及髓样和红系转录物。尽管此多谱系启动已在随后的谱系限制中得到解决,但仍可识别出淋巴样和髓样基因表达的意外共分离以及超过标称髓样限制点的潜在可能性。最后,我们证明了在HSC中诱导淋巴谱系启动需要锌指DNA结合因子Ikaros,但对于抑制与HSC下游自我更新和多能性兼容的基因程序也是必要的。综上所述,我们的研究为早期造血过程中血统潜能的引发和限制提供了新的见识,并确定了Ikaros是该过程的关键二价调节剂。 ©2009 Elsevier Inc.保留所有权利。

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