Gene expression profile of zebrafish exposed to hypoxia during development

被引:236
作者
Ton, C
Stamatiou, D
Liew, CC
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Cardiovasc Genome Unit, Boston, MA 02115 USA
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 1L5, Canada
关键词
Danio rerio; cDNA microarray;
D O I
10.1152/physiolgenomics.00128.2002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Understanding how vertebrates respond to hypoxia can have important clinical implications. Fish have evolved the ability to survive long exposure to low oxygen levels. However, little is known about the specific changes in gene expression that result from hypoxia. In this study we used a zebrafish cDNA microarray to examine the expression of > 4,500 genes in zebrafish embryos exposed to 24 h of hypoxia during development. We tested the hypotheses that hypoxia changes gene expression profile of the zebrafish embryos and that these changes can be reverted by reexposure to a normoxic (20.8% O-2) environment. Our data were consistent with both of these hypotheses: indicating that zebrafish embryos undergo adaptive changes in gene expression in response to hypoxia. Our study provides a striking genetic portrait of the zebrafish embryos' adaptive responses to hypoxic stress and demonstrates the utility of the microarray technology as a tool for analyzing complex developmental processes in the zebrafish.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 50 条
[1]   Construction of a human cardiovascular cDNA microarray: Portrait of the failing heart [J].
Barrans, JD ;
Stamatiou, D ;
Liew, CC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 280 (04) :964-969
[2]   ACTIVATION OF THE HEAT-SHOCK TRANSCRIPTION FACTOR BY HYPOXIA IN MAMMALIAN-CELLS [J].
BENJAMIN, IJ ;
KROGER, B ;
WILLIAMS, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6263-6267
[3]  
Bernier NJ, 1996, J EXP BIOL, V199, P485
[4]  
Bernier NJ, 1996, J EXP BIOL, V199, P497
[5]   COACTIVATION OF RANGTPASE AND INHIBITION OF GTP DISSOCIATION BY RAN GTP-BINDING PROTEIN RANBP1 [J].
BISCHOFF, FR ;
KREBBER, H ;
SMIRNOVA, E ;
DONG, WH ;
PONSTINGL, H .
EMBO JOURNAL, 1995, 14 (04) :705-715
[6]   Surviving hypoxia without really dying [J].
Boutilier, RG ;
St-Pierre, J .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 2000, 126 (04) :481-490
[7]   Ran-GTP coordinates regulation of microtubule nucleation and dynamics during mitotic-spindle assembly [J].
Carazo-Salas, RE ;
Gruss, OJ ;
Mattaj, IW ;
Karsenti, E .
NATURE CELL BIOLOGY, 2001, 3 (03) :228-234
[8]   Effects of p21Waf1/Cip1/Sdi1 on cellular gene expression:: Implications for carcinogenesis, senescence, and age-related diseases [J].
Chang, BD ;
Watanabe, K ;
Broude, EV ;
Fang, J ;
Poole, JC ;
Kalinichenko, TV ;
Roninson, IB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :4291-4296
[9]   The role of ARF and Rab GTPases in membrane transport [J].
Chavrier, P ;
Goud, B .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (04) :466-475
[10]   Cardiovascular genomics: Estimating the total number of genes expressed in the human cardiovascular system [J].
Dempsey, AA ;
Dzau, VJ ;
Liew, CC .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (10) :1879-1886