The case for regulating indispensable amino acid metabolism: the branched-chain alpha-keto acid dehydrogenase kinase-knockout mouse
- PMID: 17061958
- PMCID: PMC1635442
- DOI: 10.1042/BJ20061506
The case for regulating indispensable amino acid metabolism: the branched-chain alpha-keto acid dehydrogenase kinase-knockout mouse
Abstract
BCAAs (branched-chain amino acids) are indispensable (essential) amino acids that are required for body protein synthesis. Indispensable amino acids cannot be synthesized by the body and must be acquired from the diet. The BCAA leucine provides hormone-like signals to tissues such as skeletal muscle, indicating overall nutrient sufficiency. BCAA metabolism provides an important transport system to move nitrogen throughout the body for the synthesis of dispensable (non-essential) amino acids, including the neurotransmitter glutamate in the central nervous system. BCAA metabolism is tightly regulated to maintain levels high enough to support these important functions, but at the same time excesses are prevented via stimulation of irreversible disposal pathways. It is well known from inborn errors of BCAA metabolism that dysregulation of the BCAA catabolic pathways that leads to excess BCAAs and their alpha-keto acid metabolites results in neural dysfunction. In this issue of Biochemical Journal, Joshi and colleagues have disrupted the murine BDK (branched-chain alpha-keto acid dehydrogenase kinase) gene. This enzyme serves as the brake on BCAA catabolism. The impaired growth and neurological abnormalities observed in this animal show conclusively the importance of tight regulation of indispensable amino acid metabolism.
Comment on
-
Impaired growth and neurological abnormalities in branched-chain alpha-keto acid dehydrogenase kinase-deficient mice.Biochem J. 2006 Nov 15;400(1):153-62. doi: 10.1042/BJ20060869. Biochem J. 2006. PMID: 16875466 Free PMC article.
References
-
- Hutson S. M., Sweatt A. J., Lanoue K. F. Branched-chain amino acid metabolism: implications for establishing safe intakes. J. Nutr. 2005;135:1557S–1564S. - PubMed
-
- Harris R. A., Zhang B., Goodwin G. W., Kuntz M. J., Shimomura Y., Rougraff P., Dexter P., Zhao Y., Gibson R., Crabb D. W. Regulation of branched-chain α-ketoacid dehydrogenase and elucidation of a molecular basis for maple syrup urine disease. Adv. Enzyme Regul. 1990;30:245–263. - PubMed
-
- Shimomura Y., Obayashi M., Murakami T., Harris R. A. Regulation of branched-chain amino acid catabolism: nutritional and hormonal regulation of activity and expression of the branched-chain α-keto acid dehydrogenase kinase. Curr. Opin. Clin. Nutr. Metab. Care. 2001;4:419–423. - PubMed
-
- Suryawan A., Hawes J. W., Harris R. A., Shimomura Y., Jenkins A. E., Hutson S. M. A molecular model of human branched-chain amino acid metabolism. Am. J. Clin. Nutr. 1998;68:72–81. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous
