Comprehensive analysis of the mouse metabolome based on the transcriptome

被引:17
|
作者
Bono, H
Nikaido, I
Kasukawa, T
Hayashizaki, Y
Okazaki, Y
机构
[1] RIKEN, Genom Sci Ctr GSC, Yokohama Inst, Lab Genome Explorat Res Grp,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] Yokohama City Univ, Grad Sch Integrated Sci, Sci Biol Supramol Syst, Div Genom Informat Resource Explorat,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[3] NTT Software Corp, Adv Technol Dev Dept, Multimedia Dev Ctr, Naka Ku, Yokohama, Kanagawa 2318554, Japan
[4] RIKEN, Genome Sci Lab, Wako, Saitama 3510198, Japan
关键词
D O I
10.1101/gr.974603
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
The complete set of cDNAs encoding the enzymes of known metabolic pathways has not previously been available for any mammal. Here, transcripts encoding the metabolic pathways of the mouse (mouse metabolome) were reconstructed by making use of the KEGG metabolic pathway database and gene ontology (GO) assignment to the mouse representative transcript and protein set (RTPS), which contains all available mouse transcript sequences including the FANTOM set of RIKEN mouse cDNA clones. By assigning EC numbers extracted from the molecular function ontology in GO, the known mouse transcriptome was predicted to encode enzymes with 726 unique EC numbers. Of these, 648 EC numbers were newly assigned based on the FANTOM set. The mouse metabolome confirmed by cDNA analysis includes almost all of the enzymes of well known pathways such as the tricarboxylic acid cycle and urea cycle. On the other hand, analysis of enzymes required for the tryptophan metabolism pathway revealed a lack of connectivity, indicating that cDNAs/genes encoding several key enzymes remain to be identified. The information derived from coexpression from the cDNA microarray analysis of enzymes of known function may lead to identification of the missing components of the metabolome, and will add new insights into the connectivity of the mammalian metabolic pathways.
引用
收藏
页码:1345 / 1349
页数:5
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