Transcription factor (TF) networks determine cell-type identity by establishing and maintaining lineage-specific expression profiles, yet reconstruction of mammalian regulatory network models has been hampered by a lack of comprehensive functional validation of regulatory interactions. Here, we report comprehensive ChIP-Seq, transgenic and reporter gene experimental data that have allowed us to construct an experimentally validated regulatory network model for haematopoietic stem/progenitor cells (HSPCs). Model simulation coupled with subsequent experimental validation using single cell expression profiling revealed potential mechanisms for cell state stabilisation, and also how a leukaemogenic TF fusion protein perturbs key HSPC regulators. The approach presented here should help to improve our understanding of both normal physiological and disease processes.
An experimentally validated network of nine haematopoietic transcription factors reveals mechanisms of cell state stability.
经实验验证的由九种造血转录因子组成的网络揭示了细胞状态稳定性的机制
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作者:Schütte Judith, Wang Huange, Antoniou Stella, Jarratt Andrew, Wilson Nicola K, Riepsaame Joey, Calero-Nieto Fernando J, Moignard Victoria, Basilico Silvia, Kinston Sarah J, Hannah Rebecca L, Chan Mun Chiang, Nürnberg Sylvia T, Ouwehand Willem H, Bonzanni Nicola, de Bruijn Marella Ftr, Göttgens Berthold
| 期刊: | Elife | 影响因子: | 6.400 |
| 时间: | 2016 | 起止号: | 2016 Feb 22; 5:e11469 |
| doi: | 10.7554/eLife.11469 | 研究方向: | 细胞生物学 |
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