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首页> 外文期刊>Molecular and Cellular Biology >A novel transcriptional regulatory region within the core promoter of the hepatocyte growth factor gene is responsible for its inducibility by cytokines via the C/EBP family of transcription factors.
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A novel transcriptional regulatory region within the core promoter of the hepatocyte growth factor gene is responsible for its inducibility by cytokines via the C/EBP family of transcription factors.

机译:肝细胞生长因子基因核心启动子中的一个新的转录调控区负责通过细胞因子通过C / EBP转录因子家族诱导其转录。

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摘要

Hepatocyte growth factor (HGF) is an inducible cytokine that is essential for the normal growth and development of various tissues, such as the liver. To decipher the molecular mechanisms that regulate HGF gene induction at the transcriptional level, we carried out in vitro and in vivo studies on the mouse HGF gene promoter. We have identified a novel regulatory element, located between -6 and +7 bp (from the transcription start site) in the HGF basal promoter region, which binds to inducible transcription factors and dictates responsiveness to extracellular stimuli that activate this gene. The core binding sequence for the inducible cis-acting factors was determined to be TTTGCAA (-4 to +3 bp) within the HGF promoter. Competition and gel mobility supershift assays showed that these binding complexes are composed of C/EBPbeta (CCAAT/enhancer-binding protein beta) and C/EBPdelta. DNA binding analysis also revealed that the binding site for the C/EBP family of transcription factors in the HGF promoter region overlaps that of another binding protein (complex C1), which binds specifically to a novel sequence with a core binding site of ACCGGT located adjacent to the C/EBP site (-9 to -4 bp). C1 binds to this region of the promoter and represses the inducible upregulation by C/EBP through direct competition for their individual binding sites. Partial hepatectomy, which is known to activate HGF gene expression in the liver, increased C/EBP (especially C/EBPbeta) binding activity to this region of the HGF promoter. Thus, our present results provide a mechanistic explanation for the transcriptional induction of the HGF gene by extracellular signals (i.e., cytokines) that induce tissue growth and regeneration.
机译:肝细胞生长因子(HGF)是一种可诱导的细胞因子,对于各种组织(例如肝脏)的正常生长和发育必不可少。为了解释在转录水平上调节HGF基因诱导的分子机制,我们对小鼠HGF基因启动子进行了体外和体内研究。我们已经确定了一种新型的调控元件,位于HGF基础启动子区域的-6和+7 bp之间(从转录起始位点起),该元件与诱导型转录因子结合并决定了对激活该基因的细胞外刺激的响应性。在HGF启动子内,可诱导的顺式作用因子的核心结合序列被确定为TTTGCAA(-4至+3 bp)。竞争和凝胶迁移率超位移分析表明,这些结合复合物由C / EBPbeta(CCAAT /增强子结合蛋白β)和C / EBPdelta组成。 DNA结合分析还显示,HGF启动子区域中转录因子C / EBP家族的结合位点与另一种结合蛋白(复合物C1)的结合位点重叠,该结合蛋白特异性结合具有ACCGGT核心结合位点的新序列到C / EBP位点(-9至-4 bp)。 C1结合到启动子的这一区域,并通过直接竞争其单个结合位点来抑制C / EBP诱导的上调。众所周知,部分肝切除术可以激活肝脏中的HGF基因表达,从而提高了与HGF启动子这一区域的C / EBP(特别是C / EBPbeta)结合活性。因此,我们目前的结果为诱导组织生长和再生的细胞外信号(即细胞因子)对HGF基因的转录诱导提供了机械学解释。

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