An extensive (co-)expression analysis tool for the cytochrome P450 superfamily in Arabidopsis thaliana

被引:102
作者
Ehlting, Juergen [1 ]
Sauveplane, Vincent [1 ]
Olry, Alexandre [1 ]
Ginglinger, Jean-Francois [1 ]
Provart, Nicholas J. [2 ]
Werck-Reichhart, Daniele [1 ]
机构
[1] Univ Strasbourg 1, CNRS, Inst Plant Mol Biol, UPR 2357, F-67000 Strasbourg, France
[2] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON M5S 3B2, Canada
关键词
D O I
10.1186/1471-2229-8-47
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Sequencing of the first plant genomes has revealed that cytochromes P450 have evolved to become the largest family of enzymes in secondary metabolism. The proportion of P450 enzymes with characterized biochemical function(s) is however very small. If P450 diversification mirrors evolution of chemical diversity, this points to an unexpectedly poor understanding of plant metabolism. We assumed that extensive analysis of gene expression might guide towards the function of P450 enzymes, and highlight overlooked aspects of plant metabolism. Results: We have created a comprehensive database, 'CYPedia', describing P450 gene expression in four data sets: organs and tissues, stress response, hormone response, and mutants of Arabidopsis thaliana, based on public Affymetrix ATH1 microarray expression data. P450 expression was then combined with the expression of 4,130 re-annotated genes, predicted to act in plant metabolism, for co-expression analyses. Based on the annotation of co-expressed genes from diverse pathway annotation databases, co-expressed pathways were identified. Predictions were validated for most P450s with known functions. As examples, co-expression results for P450s related to plastidial functions/photosynthesis, and to phenylpropanoid, triterpenoid and jasmonate metabolism are highlighted here. Conclusion: The large scale hypothesis generation tools presented here provide leads to new pathways, unexpected functions, and regulatory networks for many P450s in plant metabolism. These can now be exploited by the community to validate the proposed functions experimentally using reverse genetics, biochemistry, and metabolic profiling.
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页数:19
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