Methylation of hypoxia-inducible factor (HIF)-1α by G9a/GLP inhibits HIF-1 transcriptional activity and cell migration.

Methylation of hypoxia-inducible factor (HIF)-1α by G9a/GLP inhibits HIF-1 transcriptional activity and cell migration.
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DOI:
10.1093/nar/gky449
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发表时间:
2018-07-27
影响因子:
14.9
通讯作者:
Luo W
Luo W
中科院分区:
生物学2区
文献类型:
--
作者:
Bao L;Chen Y;Lai HT;Wu SY;Wang JE;Hatanpaa KJ;Raisanen JM;Fontenot M;Lega B;Chiang CM;Semenza GL;Wang Y;Luo W

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缺氧诱导因子1(HIF-1)是响应缺氧的主要转录调节因子,其转录活性对癌细胞的运动至关重要。在这里,我们提出了一种新的表观遗传机制,调节HIF-1的转录活性和HIF-1依赖的胶质母细胞瘤细胞迁移的证据。赖氨酸甲基转移酶G9 a和GLP直接与HIF-1 α的α亚基(HIF-1α)结合,并在体外和体内催化HIF-1α在赖氨酸(K)674处的单甲基化和双甲基化。K674甲基化抑制人胶质母细胞瘤U251 MG细胞中HIF-1的转录活性及其下游靶基因PTGS 1、NDNF、SLC 6A 3和Linc 01132的表达。K674甲基化对HIF-1的抑制是由于HIF-1α反式激活结构域功能降低,而不是HIF-1α蛋白降解增加或HIF-1与缺氧反应元件结合受损。K674甲基化显著降低U251 MG细胞在缺氧条件下的HIF-1依赖性迁移。重要的是,我们发现G9 a在胶质母细胞瘤中被缺氧下调,这与PTGS 1表达和胶质母细胞瘤患者的生存率呈负相关。因此,我们的研究结果揭示了一个缺氧诱导的负反馈机制,维持高活性的HIF-1和细胞的流动性在人类胶质母细胞瘤。
Hypoxia-inducible factor 1 (HIF-1) is a master transcriptional regulator in response to hypoxia and its transcriptional activity is crucial for cancer cell mobility. Here we present evidence for a novel epigenetic mechanism that regulates HIF-1 transcriptional activity and HIF-1-dependent migration of glioblastoma cells. The lysine methyltransferases G9a and GLP directly bound to the α subunit of HIF-1 (HIF-1α) and catalyzed mono- and di-methylation of HIF-1α at lysine (K) 674 in vitro and in vivo. K674 methylation suppressed HIF-1 transcriptional activity and expression of its downstream target genes PTGS1, NDNF, SLC6A3, and Linc01132 in human glioblastoma U251MG cells. Inhibition of HIF-1 by K674 methylation is due to reduced HIF-1α transactivation domain function but not increased HIF-1α protein degradation or impaired binding of HIF-1 to hypoxia response elements. K674 methylation significantly decreased HIF-1-dependent migration of U251MG cells under hypoxia. Importantly, we found that G9a was downregulated by hypoxia in glioblastoma, which was inversely correlated with PTGS1 expression and survival of patients with glioblastoma. Therefore, our findings uncover a hypoxia-induced negative feedback mechanism that maintains high activity of HIF-1 and cell mobility in human glioblastoma.
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