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首页> 外文期刊>Oncogene >PIASy stimulates HIF1|[alpha]| SUMOylation and negatively regulates HIF1|[alpha]| activity in response to hypoxia
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PIASy stimulates HIF1|[alpha]| SUMOylation and negatively regulates HIF1|[alpha]| activity in response to hypoxia

机译:PIASy刺激HIF1 |α| SUMOylation并负调控HIF1 |α|缺氧反应

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摘要

Hypoxia-inducible factor-1α (HIF1α) is a crucial regulator of the cellular response to hypoxia through its regulation of genes that control erythropoiesis, angiogenesis and anaerobic metabolism. We have previously shown that HIF1α stability is regulated by SUMOylation under the hypoxic condition. However, how HIF1α became SUMOylated during hypoxia is still unknown. In this study we identify PIASy as a specific E3 ligase for hypoxia-induced HIF1α SUMOylation. Hypoxia promotes translocation of HIF1α to the nucleus to facilitate its binding to PIASy, enabling the conjugation of HIF1α by SUMO1. We further show that PIASy negatively regulates hypoxia-induced HIF1α stability and transactivation. Knocking down PIASy increases the angiogenic activity of endothelial cells. Moreover, we show an inverse relationship between expression of PIASy and tumor angiogenesis in colon cancer. Thus, we define an important role of PIASy in hypoxia signaling through promoting HIF1α SUMOylation.
机译:缺氧诱导因子-1α(HIF1α)通过调节控制红细胞生成,血管生成和厌氧代谢的基因来调节细胞对缺氧的反应。先前我们已经表明,在缺氧条件下,HIF1α的稳定性受SUMOylation的调节。然而,HIF1α在缺氧过程中如何被SUMO化仍是未知的。在这项研究中,我们确定PIASy是缺氧诱导的HIF1αSUMOylation的特异性E3连接酶。缺氧促进HIF1α向核的转运,以促进其与PIASy的结合,从而使SUMO1结合HIF1α。我们进一步表明,PIASy负调控缺氧诱导的HIF1α稳定性和反式激活。敲低PIASy可增加内皮细胞的血管生成活性。此外,我们显示了PIASy的表达与结肠癌中肿瘤血管生成之间的反比关系。因此,我们定义了PIASy通过促进HIF1αSUMOylation在缺氧信号传导中的重要作用。

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