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GATA-1 mediates auto-regulation of Gfi-1B transcription in K562 cells

机译:GATA-1介导K562细胞中Gfi-1B转录的自动调节

摘要

Gfi-1B (growth factor independence-1B) gene is an erythroid-specific transcription factor, whose expression plays an essential role in erythropoiesis. Our laboratory has previously defined the human Gfi-1B promoter region and shown that GATA-1 mediates erythroid-specific Gfi-1B transcription. By further investigating the regulation of the Gfi-1B promoter, here we report that (i) Gfi-1B transcription is negatively regulated by its own gene product, (ii) GATA-1, instead of Gfi-1B, binds directly to the Gfi-1-like sites in the Gfi-1B promoter and (iii) Gfi-1B suppresses GATA-1-mediated stimulation of Gfi-1B promoter through their protein interaction. These results not only demonstrate that interaction of GATA-1 and Gfi-1B participates in a feedback regulatory pathway in controlling the expression of the Gfi-1B gene, but also provide the first evidence that Gfi-1B can exert its repression function by acting on GATA-1-mediated transcription without direct binding to the Gfi-1 site of the target genes. Based on these data, we propose that this negative auto-regulatory feedback loop is important in restricting the expression level of Gfi-1B, thus optimizing its function in erythroid cells.
机译:Gfi-1B(生长因子独立-1B)基因是一种类红细胞特异性转录因子,其表达在促红细胞生成中起重要作用。我们的实验室以前已经定义了人Gfi-1B启动子区域,并表明GATA-1介导了类红细胞特异性Gfi-1B转录。通过进一步研究Gfi-1B启动子的调控,我们在此报告(i)Gfi-1B转录受到其自身基因产物的负调控,(ii)GATA-1而非Gfi-1B直接与Gfi结合Gfi-1B启动子中的-1-样位点;(iii)Gfi-1B通过它们的蛋白质相互作用抑制GATA-1介导的Gfi-1B启动子的刺激。这些结果不仅表明GATA-1和Gfi-1B的相互作用参与了控制Gfi-1B基因表达的反馈调节途径,而且提供了第一个证据表明Gfi-1B可以通过作用于Gfi-1B而发挥其抑制功能。 GATA-1介导的转录,不直接结合到靶基因的Gfi-1位点。基于这些数据,我们建议这种负的自动调节反馈回路在限制Gfi-1B的表达水平,从而优化其在类红细胞中的功能中很重要。

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