Fish 'n' chips: the use of microarrays for aquatic toxicology

被引:66
作者
Denslow, Nancy D. [1 ]
Garcia-Reyero, Natalia
Barber, David S.
机构
[1] Univ Florida, Dept Physiol Sci, Gainesville, FL 32610 USA
[2] Univ Florida, Ctr Environm & Human Toxicol, Gainesville, FL 32610 USA
关键词
D O I
10.1039/b612802p
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
Gene expression analysis is changing the way that we look at toxicity, allowing toxicologists to perform parallel analyses of entire transcriptomes. While this technology is not as advanced in aquatic toxicology as it is for mammalian models, it has shown promise for determining modes of action, identifying biomarkers and developing "signatures" of chemicals that can be used for field and mixture studies. A major hurdle for the use of microarrays in aquatic toxicology is the lack of sequence information for non-model species. Custom arrays based on gene libraries enriched for genes that are expressed in response to specific contaminants have been used with excellent success for some non-model species, suggesting that this approach will work well for ecotoxicology and spurring on the sequencing of cDNA libraries for species of interest. New sequencing technology and development of repositories for gene expression data will accelerate the use of microarrays in aquatic toxicology. Notwithstanding the preliminary successes that have been achieved even with partial cDNA libraries printed on arrays, ecological samples present elevated challenges for this technology due to the high degree of variation of the samples. Furthermore, recent studies that show nonlinear toxic responses for ecological species underscore the necessity of establishing time and dose dependence of effects on gene expression and comparing these results with traditional markers of toxicity. To realize the full potential of microarrays, researchers must do the experiments required to bridge the gap between the 'omics' technologies and traditional toxicology to demonstrate that microarrays have predictive value in ecotoxicology.
引用
收藏
页码:172 / 177
页数:6
相关论文
共 62 条
[21]  
2-7
[22]   Molecular biology of channel catfish brain cytochrome P450 aromatase (CYP19A2): cloning, preovulatory induction of gene expression, hormonal gene regulation and analysis of promoter region [J].
Kazeto, Y ;
Trant, JM .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2005, 35 (03) :571-583
[23]   Ontological analysis of gene expression data: current tools, limitations, and open problems [J].
Khatri, P ;
Draghici, S .
BIOINFORMATICS, 2005, 21 (18) :3587-3595
[24]   Microarray analysis of altered gene expression in murine fibroblasts transformed by nickel(II) to nickel(II)-resistant malignant phenotype [J].
Kowara, R ;
Karaczyn, A ;
Cheng, RYS ;
Salnikow, K ;
Kasprzak, KS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 205 (01) :1-10
[25]   Modeling liver cancer using zebrafish - A comparative oncogenomics approach [J].
Lam, Siew Hong ;
Gong, Zhiyuan .
CELL CYCLE, 2006, 5 (06) :573-577
[26]   Anthropogenic, ecological and genetic factors in extinction and conservation [J].
Lande, R .
RESEARCHES ON POPULATION ECOLOGY, 1998, 40 (03) :259-269
[27]  
Larkin Patrick, 2003, Environmental Health Perspectives, V111, P29
[28]  
Lee PH, 1998, MOL REPROD DEV, V49, P112, DOI 10.1002/(SICI)1098-2795(199802)49:2&lt
[29]  
112::AID-MRD2&gt
[30]  
3.0.CO