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

机译:在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

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摘要

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.
机译:c-Myb转录因子是造血细胞发育的重要调节器。 c-Myb在未成熟的造血细胞中表达,并在血统命运选择,细胞周期进程以及骨髓以及B和T淋巴祖细胞的分化中发挥直接作用。作为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。但是,我们对这些程序的理解还不完整。在这里,我们报告一套新的c-Myb靶基因,使用组合方法鉴定:通过2种不同的siRNA进行特异性c-Myb敲低和随后的整体表达谱分析,以及c-Myb与靶启动子直接结合的确认通过ChIP分析。这两种方法的结合以及其他验证方法(如在报道基因分析中克隆和测试启动子),证实MYADM,LMO2,GATA2,STAT5A和IKZF1是c-Myb的靶基因。使用染色体构象捕获的其他研究表明,c-Myb目标基因可能直接相互相互作用,表明这些基因可能受到协调调控。在确定的5个新靶基因中,有3个是转录因子,一个是转录共调节子,支持c-Myb作为控制造血系统中其他转录调节子表达的主调节子。

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