Cellular oxygen sensing: Importins and exportins are mediators of intracellular localisation of prolyl-4-hydroxylases PHD1 and PHD2

被引:33
作者
Steinhoff, Amrei [1 ]
Pientka, Friederike Katharina [1 ]
Moeckel, Sylvia [1 ]
Kettelhake, Antje [1 ]
Hartmann, Enno [2 ]
Koehler, Matthias [3 ,4 ,5 ]
Depping, Reinhard [1 ]
机构
[1] Med Univ Lubeck, Dept Physiol, Ctr Struct & Cell Biol Med, D-23538 Lubeck, Germany
[2] Med Univ Lubeck, Dept Biol, Ctr Struct & Cell Biol Med, D-23538 Lubeck, Germany
[3] Ostsee Clin, Ctr Nephrol & Hypertens, D-24351 Damp, Germany
[4] Reha Clin Damp, D-24351 Damp, Germany
[5] Univ Kiel, Dept Hypertens & Nephrol, D-24105 Kiel, Germany
关键词
Hypoxia; HIF; Prolyl-hydroxylase; Importin; NLS; NES; Leptomycin; HYDROXYLASE DOMAIN PROTEIN-2; HYPOXIA-INDUCIBLE FACTORS; TUMOR-SUPPRESSOR PROTEIN; CRYSTALLOGRAPHIC ANALYSIS; NUCLEAR TRANSLOCATION; KARYOPHERIN ALPHA; HIF-ALPHA; RECOGNITION; SEQUENCES; SIGNAL;
D O I
10.1016/j.bbrc.2009.07.090
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
Hypoxia-inducible factors are crucial in the regulatory process of oxygen homeostasis of vertebrate cells. Inhibition of prolyl hydroxylation of HIF-alpha subunits by prolyl-hydroxylases (PHD1, PHD2 and PHD3) leads to transcription of a greater number of hypoxia responsive genes. We have investigated the subcellular distribution and the molecular mechanisms regulating the intracellular allocation of PHD1 and PHD2. As reported earlier we find PHD1 located exclusively in the nucleus. We demonstrate that nuclear import of PHD1 occurs importin alpha/beta dependently and relies on a nuclear localisation signal (NLS). By contrast PHD2 is cycling between nucleus and cytoplasm, and nuclear import seems to be independent of "classical" importin alpha/beta receptors. Furthermore, we reveal that the exit of PHD2 from the nucleus requires CRM1 and the N-terminal 100 amino acids of the protein. Our findings provide new insights into the mechanisms of the regulation of the oxygen sensor cascade of PHDs in different cellular compartments. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:705 / 711
页数:7
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