The regulation, localization, and functions of oxygen-sensing prolyl hydroxylase PHD3

被引:40
|
作者
Jaakkola, Panu M. [1 ,2 ,3 ]
Rantanen, Krista [1 ,2 ]
机构
[1] Turku Univ, Turku Ctr Biotechnol, FIN-20520 Turku, Finland
[2] Abo Akad Univ, FIN-20520 Turku, Finland
[3] Turku Univ Hosp, Dept Radiotherapy & Oncol, FIN-20520 Turku, Finland
基金
芬兰科学院;
关键词
aggresome; egg-laying deficiency protein nine-like protein or prolyl 4-hydroxylase domain protein 3 (EGLN); hypoxia; hypoxia-inducible factor (HIF); oxygen sensor; p62; von Hippel-Lindau protein (pVHL); FACTOR-RESPONSIVE GENE; INDUCIBLE FACTOR HIF; NEURONAL APOPTOSIS; CELL-METABOLISM; DIRECT BINDING; CANCER-CELLS; HYPOXIA; ALPHA; EXPRESSION; GROWTH;
D O I
10.1515/hsz-2012-0330
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prolyl 4-hydroxylase domain protein 3 (PHD3) belongs to 2-oxoglutarate and iron-dependent dioxygenases. Together with the two closest paralogues, PHD1 and PHD2, these enzymes have been identified as cellular oxygen sensors that can mark the hypoxia-inducible factor alpha (HIF-alpha) for von Hippel-Lindau protein-mediated proteasomal destruction. Although having overlapping functions with PHD1 and PHD2, PHD3 markedly differs from the two isoforms. PHD3 shows a different expression pattern and subcellular localization as well as activity under low oxygen tension. Moreover, it has the widest range of non-HIF targets underlying its diverse functions. The functions of PHD3 differ depending on the cell type and also partially on the microenvironmental conditions it is expressed at. Under normoxia, PHD3 has been shown to be proapoptotic, but under hypoxia, it can have cell survival or proliferation-supporting functions. Here we discuss the regulation, targets, and functions of PHD3.
引用
收藏
页码:449 / 457
页数:9
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