Koizume Shiro, Yokota Naho, Miyagi Etsuko, Hirahara Fumiki, Tsuchiya Eiju, Miyagi Yohei
Molecular Pathology & Genetics Division, Kanagawa Cancer Center Research Institute, 1-1-2 Nakao, Asahi-ku, Yokohama 241-0815, Japan.
Biochem Biophys Res Commun. 2008 Jun 27;371(2):251-5. doi: 10.1016/j.bbrc.2008.04.042. Epub 2008 Apr 28.
Here, we demonstrate by chromatin immunoprecipitation that the binding of hypoxia-inducible factors to gene regulatory regions is differentially influenced in cancer cells. Binding of HIF-2alpha varies depending on hypoxic conditions, although HIF-1alpha is constantly bound to these regions. We found by RNA interference experiments that HIF-2alpha plays a minor role in VEGF gene upregulation under hypoxia or CoCl(2) treatment, even when both HIFs are similarly bound to the promoter region. HIF-2alpha activated or suppressed the ENO1 gene under various conditions, irrespective of promoter binding. We additionally found that HIF dependence on EPO gene induction could be altered depending on the conditions, irrespective of the binding pattern of HIFs. These results demonstrate that, unlike HIF-1alpha, HIF-2alpha differentially binds and regulates transcription under hypoxia.
在此,我们通过染色质免疫沉淀证明,缺氧诱导因子与基因调控区域的结合在癌细胞中受到不同影响。尽管HIF-1α始终与这些区域结合,但HIF-2α的结合会因缺氧条件而异。我们通过RNA干扰实验发现,即使在缺氧或氯化钴处理下,当两种缺氧诱导因子都类似地结合到启动子区域时,HIF-2α在VEGF基因上调中起的作用较小。在各种条件下,无论启动子结合情况如何,HIF-2α都会激活或抑制ENO1基因。我们还发现,无论缺氧诱导因子的结合模式如何,缺氧诱导因子对EPO基因诱导的依赖性可能会因条件而异。这些结果表明,与HIF-1α不同,HIF-2α在缺氧条件下以不同方式结合并调节转录。