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Genetic networks of liver metabolism revealed by integration of metabolic and transcriptional profiling.

Publication ,  Journal Article
Ferrara, CT; Wang, P; Neto, EC; Stevens, RD; Bain, JR; Wenner, BR; Ilkayeva, OR; Keller, MP; Blasiole, DA; Kendziorski, C; Yandell, BS ...
Published in: PLoS Genet
March 14, 2008

Although numerous quantitative trait loci (QTL) influencing disease-related phenotypes have been detected through gene mapping and positional cloning, identification of the individual gene(s) and molecular pathways leading to those phenotypes is often elusive. One way to improve understanding of genetic architecture is to classify phenotypes in greater depth by including transcriptional and metabolic profiling. In the current study, we have generated and analyzed mRNA expression and metabolic profiles in liver samples obtained in an F2 intercross between the diabetes-resistant C57BL/6 leptin(ob/ob) and the diabetes-susceptible BTBR leptin(ob/ob) mouse strains. This cross, which segregates for genotype and physiological traits, was previously used to identify several diabetes-related QTL. Our current investigation includes microarray analysis of over 40,000 probe sets, plus quantitative mass spectrometry-based measurements of sixty-seven intermediary metabolites in three different classes (amino acids, organic acids, and acyl-carnitines). We show that liver metabolites map to distinct genetic regions, thereby indicating that tissue metabolites are heritable. We also demonstrate that genomic analysis can be integrated with liver mRNA expression and metabolite profiling data to construct causal networks for control of specific metabolic processes in liver. As a proof of principle of the practical significance of this integrative approach, we illustrate the construction of a specific causal network that links gene expression and metabolic changes in the context of glutamate metabolism, and demonstrate its validity by showing that genes in the network respond to changes in glutamine and glutamate availability. Thus, the methods described here have the potential to reveal regulatory networks that contribute to chronic, complex, and highly prevalent diseases and conditions such as obesity and diabetes.

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Published In

PLoS Genet

DOI

EISSN

1553-7404

Publication Date

March 14, 2008

Volume

4

Issue

3

Start / End Page

e1000034

Location

United States

Related Subject Headings

  • RNA, Messenger
  • Quantitative Trait Loci
  • Phenotype
  • Models, Genetic
  • Mice, Mutant Strains
  • Mice, Inbred C57BL
  • Mice
  • Metabolic Networks and Pathways
  • Male
  • Liver
 

Citation

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Ferrara, C. T., Wang, P., Neto, E. C., Stevens, R. D., Bain, J. R., Wenner, B. R., … Attie, A. D. (2008). Genetic networks of liver metabolism revealed by integration of metabolic and transcriptional profiling. PLoS Genet, 4(3), e1000034. https://doi.org/10.1371/journal.pgen.1000034
Ferrara, Christine T., Ping Wang, Elias Chaibub Neto, Robert D. Stevens, James R. Bain, Brett R. Wenner, Olga R. Ilkayeva, et al. “Genetic networks of liver metabolism revealed by integration of metabolic and transcriptional profiling.PLoS Genet 4, no. 3 (March 14, 2008): e1000034. https://doi.org/10.1371/journal.pgen.1000034.
Ferrara CT, Wang P, Neto EC, Stevens RD, Bain JR, Wenner BR, et al. Genetic networks of liver metabolism revealed by integration of metabolic and transcriptional profiling. PLoS Genet. 2008 Mar 14;4(3):e1000034.
Ferrara, Christine T., et al. “Genetic networks of liver metabolism revealed by integration of metabolic and transcriptional profiling.PLoS Genet, vol. 4, no. 3, Mar. 2008, p. e1000034. Pubmed, doi:10.1371/journal.pgen.1000034.
Ferrara CT, Wang P, Neto EC, Stevens RD, Bain JR, Wenner BR, Ilkayeva OR, Keller MP, Blasiole DA, Kendziorski C, Yandell BS, Newgard CB, Attie AD. Genetic networks of liver metabolism revealed by integration of metabolic and transcriptional profiling. PLoS Genet. 2008 Mar 14;4(3):e1000034.

Published In

PLoS Genet

DOI

EISSN

1553-7404

Publication Date

March 14, 2008

Volume

4

Issue

3

Start / End Page

e1000034

Location

United States

Related Subject Headings

  • RNA, Messenger
  • Quantitative Trait Loci
  • Phenotype
  • Models, Genetic
  • Mice, Mutant Strains
  • Mice, Inbred C57BL
  • Mice
  • Metabolic Networks and Pathways
  • Male
  • Liver