The hypoxic proteome is influenced by gene-specific changes in mRNA translation

被引:99
作者
Koritzinsky, M [1 ]
Seigneuric, R [1 ]
Magagnin, MG [1 ]
van den Beucken, T [1 ]
Lambin, P [1 ]
Wouters, BG [1 ]
机构
[1] Dept Radiat Oncol, Res Inst Growth & Dev, MAASTRO Lab, NL-6200 MD Maastricht, Netherlands
关键词
hypoxia; translation; microarray;
D O I
10.1016/j.radonc.2005.06.036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: Hypoxia causes a rapid reduction in mRNA translation efficiency. This inhibition does not affect all mRNA species to the same extent and can therefore contribute significantly to hypoxia-induced differential protein expression. Our aim in this study was to characterize changes in gene expression during acute hypoxia and evaluate the contribution of regulation via mRNA translation on these changes. For each gene, the contribution of changes in mRNA abundance versus mRNA translation was determined. Materials and methods: DU145 prostate carcinoma cells were exposed to 4 h of hypoxia (<0.02% O-2). Efficiently translated mRNAs were isolated by sedimentation through a sucrose gradient. Affymetrix microarray technology was used to evaluate both the transcriptional and translational contribution to gene expression. Results were validated by quantitative PCR. Results: One hundred and twenty genes were more than 4-fold upregulated by hypoxia in the efficiently translated fraction of mRNA, in comparison to only 76 genes at the level of transcription. Of the 50 genes demonstrating the largest changes in translation, 11 were found to be more than 2-fold over represented in the translated fraction in comparison to their overall transcriptional level. The gene with the highest translational contribution to its induction was CITED-2, which is a negative regulator of HIF-1 transcriptional activity. Conclusions: Gene-specific regulation of mRNA translation contributes significantly to differential gene expression during hypoxia. (C) 2005 Elsevier Ireland Ltd.
引用
收藏
页码:177 / 186
页数:10
相关论文
共 64 条
[11]   Mitochondrial reactive oxygen species control the transcription factor CHOP-10/GADD153 and adipocyte differentiation -: A mechanism for hypoxia-dependent effect [J].
Carrière, A ;
Carmona, MC ;
Fernandez, Y ;
Rigoulet, M ;
Wenger, RH ;
Pénicaud, L ;
Casteilla, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (39) :40462-40469
[12]  
De Jaeger K, 2001, BRIT J CANCER, V84, P1280
[13]  
Denko N, 2000, CLIN CANCER RES, V6, P480
[14]   Hypoxia-mediated down-regulation of bid and bax in tumors occurs via hypoxia-inducible factor 1-dependent and -independent mechanisms and contributes to drug resistance [J].
Erler, JT ;
Cawthorne, CJ ;
Williams, KJ ;
Koritzinsky, M ;
Wouters, BG ;
Wilson, C ;
Miller, C ;
Demonacos, C ;
Stratford, IJ ;
Dive, C .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (07) :2875-2889
[15]   Effect of VEGF receptor-2 antibody on vascular function and oxygenation in spontaneous and transplanted tumors [J].
Fenton, BM ;
Paoni, SF ;
Ding, I .
RADIOTHERAPY AND ONCOLOGY, 2004, 72 (02) :221-230
[16]   Structural basis for negative regulation of hypoxia-inducible factor-1α by CITED2 [J].
Freedman, SJ ;
Sun, ZYJ ;
Kung, AL ;
France, DS ;
Wagner, G ;
Eck, MJ .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (07) :504-512
[17]   Oxygenation predicts radiation response and survival in patients with cervix cancer [J].
Fyles, AW ;
Milosevic, M ;
Wong, R ;
Kavanagh, MC ;
Pintilie, M ;
Sun, A ;
Chapman, W ;
Levin, W ;
Manchul, L ;
Keane, TJ ;
Hill, RP .
RADIOTHERAPY AND ONCOLOGY, 1998, 48 (02) :149-156
[18]   REGULATION OF ANGIOGENIC GROWTH-FACTOR EXPRESSION BY HYPOXIA, TRANSITION-METALS, AND CHELATING-AGENTS [J].
GLEADLE, JM ;
EBERT, BL ;
FIRTH, JD ;
RATCLIFFE, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 268 (06) :C1362-C1368
[19]   Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours [J].
Graeber, TG ;
Osmanian, C ;
Jacks, T ;
Housman, DE ;
Koch, CJ ;
Lowe, SW ;
Giaccia, AJ .
NATURE, 1996, 379 (6560) :88-91
[20]   Regulated translation initiation controls stress-induced gene expression in mammalian cells [J].
Harding, HP ;
Novoa, I ;
Zhang, YH ;
Zeng, HQ ;
Wek, R ;
Schapira, M ;
Ron, D .
MOLECULAR CELL, 2000, 6 (05) :1099-1108