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Hypoxic activation of the atrial natriuretic peptide gene promoter through direct and indirect actions of hypoxia-inducible factor-1

机译:通过缺氧诱导因子-1的直接和间接作用低氧激活心钠素基因启动子

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pAtrial natriuretic peptide (ANP) is a cardiac peptide, the transcription of which is up-regulated in the ischaemic ventricle. However, the molecular mechanism of ANP induction is unclear. This study demonstrated that ANP mRNA expression in rat ventricular myocardium is induced in an early phase of ischaemia, preceded by hypoxia-inducible factor-1 (HIF-1) α expression. The ANP gene was also induced by hypoxia or HIF-1 inducers such as CoClsub2/sub and desferrioxamine in H9c2 and neonatal cardiomyocytes. The 2307bp 5′-flanking region of the rat ANP gene was cloned and fused to the luciferase gene. Evidence of the promoter activity was only apparent in the myocytes and was induced by hypoxia and HIF-1 inducers. The overexpression of HIF-1α markedly enhanced ANP promoter activity, and a dominant-negative isoform completely suppressed it. We demonstrated that the promoter regions are essential for hypoxic ANP induction. One promoter region, containing the HIF-1-binding sequence, is regulated directly by HIF-1. The other region is also activated by HIF-1 despite having no HIF-1-binding sequence. These results suggest that HIF-1 enhances the transactivation of the ANP gene in hypoxic myocytes, implying that stimulation of the ANP promoter by HIF-1 may in fact be responsible for the induction of the ANP gene in ischaemic ventricular myocardium./p
机译:心房利钠肽(ANP)是心脏肽,在缺血性心室中其转录上调。但是,ANP诱导的分子机制尚不清楚。这项研究表明,大鼠缺血心肌的早期诱导了ANP mRNA的表达,随后是缺氧诱导因子1(HIF-1)α的表达。 ANP基因也被低氧或HIF-1诱导物如CoCl 2 和去铁胺在H9c2和新生儿心肌细胞中诱导。克隆了大鼠ANP基因的2307bp 5'侧翼区域,并将其与荧光素酶基因融合。启动子活性的证据仅在心肌细胞中明显,并且是由缺氧和HIF-1诱导剂诱导的。 HIF-1α的过表达显着增强了ANP启动子的活性,而显性负性的亚型则完全抑制了它。我们证明了启动子区域对于缺氧ANP诱导至关重要。一个包含HIF-1结合序列的启动子区域直接由HIF-1调控。尽管没有HIF-1结合序列,但另一个区域也被HIF-1激活。这些结果表明,HIF-1增强了缺氧心肌细胞中ANP基因的反式激活,这暗示着HIF-1刺激ANP启动子实际上可能是缺血性心室心肌中ANP基因的诱导。

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