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Physiol. Genomics (June 17, 2008). doi:10.1152/physiolgenomics.00007.2008
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Submitted on January 9, 2008
Accepted on June 17, 2008

Characterization of dietary protein dependent amino acid metabolism by linking free amino acids with transcriptional profiles through analysis of correlation

Yasushi Noguchi1*, Nahoko Shikata2, Yasufumi Furuhata2, Takeshi Kimura3, and Michio Takahashi2

1 Research Institute for Health Fundamentals, Ajinomoto Co., Inc., Kawasaki, Kanagawa, Japan
2 Research Institute for Health Fundamentals, Ajinomoto Co., Inc., Kawasaki, Japan
3 Quality Assurance & External Scientific Affairs Department, Ajinomoto Co., Inc., Tokyo, Japan

* To whom correspondence should be addressed. E-mail: yasushi_noguchi{at}ajinomoto.com.

This study aims to characterize diet dependent amino acid metabolism by linking profiles of amino acids concentrations (aminograms) with transcript datasets through the analysis of correlation. We used a dietary model of protein restriction-to-excess, where rats were fed diets with different levels of casein (5, 10, 15, 20, 30, 50 and 70%) for 2 weeks. Twenty-five different amino acids in the plasma, liver, kidney, small intestine and muscle, and 71 gene transcripts in these compartments were measured together with general physiologic variables. Under low-protein diet (LPD) condition, the plasma aminogram for EAAs and EAA were alike to the liver and the small intestine one, respectively. Under high-protein diet (HPD), however, the plasma aminogram for EAAs was changed to be alike with muscle one, while that of NEAA was similar with that of both liver and muscle. To assess the impact of gene expressions in each tissue on the plasma aminograms, correlations were obtained between aminograms and transcripts in each tissue under a diet with different protein levels. Based on the correlations obtained, amino acids and transcripts were systematically connected and then metabolite-to-gene network was constructed for either LPD or HPD condition. The networks obtained and some other metabolically meaningful relationships such as ureagenesis and serine metabolism clearly illustrated activation of either body protein breakdown with LPD or amino acid catabolism with HPD.







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