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K562细胞中c-Myb靶基因的鉴定揭示了c-Myb作为主要调控因子的作用。

Identification of c-Myb Target Genes in K562 Cells Reveals a Role for c-Myb as a Master Regulator.

作者信息

Lorenzo Petra Isabel, Brendeford Elen Margrethe, Gilfillan Siv, Gavrilov Alexey A, Leedsak Marit, Razin Sergey V, Eskeland Ragnhild, Sæther Thomas, Gabrielsen Odd Stokke

机构信息

Department of Molecular Biosciences, University of Oslo, Oslo, Norway.

出版信息

Genes Cancer. 2011 Aug;2(8):805-17. doi: 10.1177/1947601911428224.

Abstract

The c-Myb transcription factor is an important regulator of hematopoietic cell development. c-Myb is expressed in immature hematopoietic cells and plays a direct role in lineage fate selection, cell cycle progression, and differentiation of myeloid as well as B- and T-lymphoid progenitor cells. As a DNA-binding transcription factor, c-Myb regulates specific gene programs through activation of target genes. Still, our understanding of these programs is incomplete. Here, we report a set of novel c-Myb target genes, identified using a combined approach: specific c-Myb knockdown by 2 different siRNAs and subsequent global expression profiling, combined with the confirmation of direct binding of c-Myb to the target promoters by ChIP assays. The combination of these 2 approaches, as well as additional validation such as cloning and testing the promoters in reporter assays, confirmed that MYADM, LMO2, GATA2, STAT5A, and IKZF1 are target genes of c-Myb. Additional studies, using chromosome conformation capture, demonstrated that c-Myb target genes may directly interact with each other, indicating that these genes may be coordinately regulated. Of the 5 novel target genes identified, 3 are transcription factors, and one is a transcriptional co-regulator, supporting a role of c-Myb as a master regulator controlling the expression of other transcriptional regulators in the hematopoietic system.

摘要

c-Myb转录因子是造血细胞发育的重要调节因子。c-Myb在未成熟造血细胞中表达,在谱系命运选择、细胞周期进程以及髓系和B淋巴细胞及T淋巴细胞祖细胞的分化中发挥直接作用。作为一种DNA结合转录因子,c-Myb通过激活靶基因来调节特定的基因程序。然而,我们对这些程序的理解并不完整。在此,我们报告了一组新的c-Myb靶基因,采用了一种联合方法进行鉴定:通过2种不同的小干扰RNA(siRNA)特异性敲低c-Myb,随后进行全基因组表达谱分析,并结合染色质免疫沉淀(ChIP)试验来确认c-Myb与靶启动子的直接结合。这两种方法的结合,以及如克隆和在报告基因试验中测试启动子等额外的验证,证实了MYADM、LMO2、GATA2、STAT5A和IKZF1是c-Myb的靶基因。使用染色体构象捕获技术的进一步研究表明,c-Myb靶基因可能直接相互作用,这表明这些基因可能受到协同调控。在鉴定出的5个新靶基因中,有3个是转录因子,1个是转录共调节因子,这支持了c-Myb作为主要调节因子在造血系统中控制其他转录调节因子表达的作用。

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