Vaux E C, Wood S M, Cockman M E, Nicholls L G, Yeates K M, Pugh C W, Maxwell P H, Ratcliffe P J
Wellcome Trust Center for Human Genetics, The Henry Wellcome Building of Genomic Medicine, Roosevelt Dr., Oxford OX3 7BN, United Kingdom.
J Biol Chem. 2001 Nov 23;276(47):44323-30. doi: 10.1074/jbc.M104678200. Epub 2001 Sep 12.
Hypoxia-inducible factor (HIF) mediates a widespread transcriptional response to hypoxia through binding to cis-acting DNA sequences termed hypoxia response elements (HREs). Activity of the transcriptional complex is suppressed in the presence of oxygen by processes that include the targeting of HIF-alpha subunits for ubiquitin-mediated proteolysis. To provide further insights into these processes we constructed Chinese hamster ovary (CHO) cells bearing stably integrated plasmids that expressed HRE-linked surface antigens and used these cells in genetic screens for mutants that demonstrated constitutive up-regulation of HRE activity. From mutagenized cultures, clones were isolated that demonstrated up-regulation of HRE activity and increased HIF-1alpha protein levels in normoxic culture. Transfection and cell fusion studies suggested that these cells possess recessive defects that affect one or more pathways involved in HIF-alpha proteolysis. Two lines were demonstrated to harbor truncating mutations in the von Hippel-Lindau (VHL) tumor suppressor gene. In these cells, defects in ubiquitylation of exogenous human HIF-1alpha in vitro could be complemented by wild type pVHL, and re-expression of a wild type VHL gene restored a normal pattern of HIF/HRE activity, demonstrating the critical dependence of HIF regulation on pVHL in CHO cells. In contrast, other mutant cells had no demonstrable mutation in the VHL gene, and ubiquitylated exogenous HIF-1alpha normally, suggesting that they contain defects at other points in the oxygen-regulated processing of HIF-alpha subunits.
缺氧诱导因子(HIF)通过与称为缺氧反应元件(HREs)的顺式作用DNA序列结合,介导对缺氧的广泛转录反应。在有氧存在的情况下,转录复合物的活性通过包括将HIF-α亚基靶向泛素介导的蛋白水解等过程而受到抑制。为了进一步深入了解这些过程,我们构建了稳定整合表达与HRE相连的表面抗原的质粒的中国仓鼠卵巢(CHO)细胞,并将这些细胞用于遗传筛选,以寻找显示HRE活性组成性上调的突变体。从诱变培养物中分离出克隆,这些克隆在常氧培养中显示出HRE活性上调和HIF-1α蛋白水平增加。转染和细胞融合研究表明,这些细胞具有隐性缺陷,影响参与HIF-α蛋白水解的一个或多个途径。有两条细胞系被证明在冯·希佩尔-林道(VHL)肿瘤抑制基因中存在截短突变。在这些细胞中,野生型pVHL可补充体外外源性人HIF-1α泛素化的缺陷,野生型VHL基因的重新表达恢复了HIF/HRE活性的正常模式,证明了CHO细胞中HIF调节对pVHL的关键依赖性。相比之下,其他突变细胞在VHL基因中没有可检测到的突变,并且外源性HIF-1α的泛素化正常,这表明它们在HIF-α亚基的氧调节加工的其他点存在缺陷。