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在 T 细胞中,Ets 因子对小鼠和人类的 Fli1 基因有相似的调控作用。

The mouse and human Fli1 genes are similarly regulated by Ets factors in T cells.

机构信息

Division of Rheumatology, Department of Medicine, Children's Research Institute, Medical University of South Carolina, 96 Jonathon Lucas Street, Charleston, SC 29425, USA.

出版信息

Genes Immun. 2010 Mar;11(2):161-72. doi: 10.1038/gene.2009.73. Epub 2009 Oct 15.

Abstract

Fli1 is a member of the Ets family of transcription factors and is preferentially expressed in hematopoietic cell lineages. Its expression level is linked to the pathogenesis of lupus. In this study, we identified mechanisms involved in the transcriptional regulation of the mouse and human Fli1 promoters. We show that the Fli1 promoter is upregulated by Ets factors Ets1, Ets2, Fli1 and Elf1 either alone or in combination with GATA factors, but is inhibited by Tel. In vitro binding studies show that Elf1, Tel and Fli1 in T cells bind the three Ets-binding sites in the murine Fli1 proximal promoter. We identified transcription factor-binding sites in the human Fli1 promoter region that function in T cells in a similar manner to those in the mouse promoter. Furthermore, we show similar binding of Ets factors to the endogenous mouse and human Fli1 promoters in T cells and knocking down Ets1 results in an upregulation of Fli1 expression. Together, these results suggest that the human and mouse genes are regulated similarly and that Ets1 may be important in preventing the overexpression of Fli1 in T cells. This report lays the groundwork for identifying targets for manipulating Fli1 expression as a possible therapeutic approach.

摘要

Fli1 是 Ets 转录因子家族的成员,优先表达于造血细胞谱系。其表达水平与狼疮的发病机制有关。在这项研究中,我们确定了参与调控小鼠和人 Fli1 启动子转录的机制。我们发现,Ets 因子 Ets1、Ets2、Fli1 和 Elf1 可单独或与 GATA 因子一起上调 Fli1 启动子,但 Tel 会抑制其表达。体外结合研究表明,Elf1、Tel 和 Fli1 在 T 细胞中结合了小鼠 Fli1 近端启动子中的三个 Ets 结合位点。我们鉴定了人 Fli1 启动子区域中的转录因子结合位点,这些位点在 T 细胞中以类似于小鼠启动子的方式发挥作用。此外,我们还表明,Ets 因子在 T 细胞中与内源性小鼠和人 Fli1 启动子的结合相似,敲低 Ets1 会导致 Fli1 表达上调。综上所述,这些结果表明人类和小鼠基因的调控方式相似,Ets1 可能在防止 T 细胞中 Fli1 过度表达方面很重要。本报告为确定作为一种可能的治疗方法来操纵 Fli1 表达的靶标奠定了基础。

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