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c-Myc mediates a hypoxia-induced decrease in acetylated histone H4

机译:c-Myc介导缺氧诱导的乙酰化组蛋白H4减少

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摘要

Global acetylation of histone H4 is a mark of gene transcriptional activation. The c-Myc transcription factor binds to specific DNA sites in cellular chromatin and induces the acetylation of histone H4. In this study, hypoxia (1% Oxygen) induced a decrease in both global acetylated histone H4 (AcH4) and c-Myc in human lung carcinoma A549 cells and in human bronchial epithelial Beas-2B cells, The decline was more striking in A549 cells compared to Beas2-B cells, when cells were exposed to hypoxic stress for 24 h. Further studies showed that these alterations of global AcH4 can be attributed to the decrease in c-Myc protein levels. While hypoxia-induced gene activation is known to be mediated by Hypoxia Response Elements (HRE), the mechanism for down-regulation of genes by hypoxia is not known. The decrease in c-Myc protein levels induced by hypoxia may contribute to hypoxia-induced gene repression.
机译:组蛋白H4的整体乙酰化是基因转录激活的标志。 c-Myc转录因子与细胞染色质中的特定DNA位点结合,并诱导组蛋白H4的乙酰化。在这项研究中,低氧(1%氧气)诱导了人肺癌A549细胞和人支气管上皮Beas-2B细胞中总体乙酰化组蛋白H4(AcH4)和c-Myc的降低,在A549细胞中下降更为明显与Beas2-B细胞相比,当细胞暴露于低氧胁迫24小时时。进一步的研究表明,总体AcH4的这些改变可归因于c-Myc蛋白水平的降低。尽管已知缺氧诱导的基因激活是由缺氧反应元件(HRE)介导的,但由缺氧引起的基因下调的机制尚不清楚。缺氧诱导的c-Myc蛋白水平降低可能导致缺氧诱导的基因抑制。

著录项

  • 来源
    《Biochimie》 |2009年第10期|1307-1310|共4页
  • 作者

    Qin Li; Max Costa;

  • 作者单位

    New York University School of Medicine, Nelson Institute of Environmental Medicine, 57 Old Forge Road, Tuxedo, NY 10987, USA;

    New York University School of Medicine, Nelson Institute of Environmental Medicine, 57 Old Forge Road, Tuxedo, NY 10987, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    hypoxia; c-Myc; acetylation; histone H4;

    机译:缺氧c-Myc;乙酰化组蛋白H4;
  • 入库时间 2022-08-18 01:24:08

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