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一个经实验验证的由九个造血转录因子组成的网络揭示了细胞状态稳定性的机制。

An experimentally validated network of nine haematopoietic transcription factors reveals mechanisms of cell state stability.

作者信息

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

机构信息

Department of Haematology, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.

Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.

出版信息

Elife. 2016 Feb 22;5:e11469. doi: 10.7554/eLife.11469.

Abstract

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.

摘要

转录因子(TF)网络通过建立和维持谱系特异性表达谱来决定细胞类型身份,然而哺乳动物调控网络模型的重建一直受到调控相互作用缺乏全面功能验证的阻碍。在这里,我们报告了全面的染色质免疫沉淀测序(ChIP-Seq)、转基因和报告基因实验数据,这些数据使我们能够构建一个经过实验验证的造血干细胞/祖细胞(HSPCs)调控网络模型。模型模拟结合随后使用单细胞表达谱进行的实验验证,揭示了细胞状态稳定的潜在机制,以及白血病相关转录因子融合蛋白如何扰乱关键的造血干细胞/祖细胞调节因子。本文提出的方法应有助于增进我们对正常生理和疾病过程的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1879/4798972/5d04a257fca3/elife-11469-fig1.jpg

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