Identification of two human dimethylarginine dimethylaminohydrolases with distinct tissue distributions and homology with microbial arginine deiminases

Author:

LEIPER James M.1,MARIA Joanne SANTA1,CHUBB Ann2,MACALLISTER Raymond J.3,CHARLES Ian G.2,WHITLEY Guy St. J.1,VALLANCE Patrick3

Affiliation:

1. Department of Cellular and Molecular Sciences, St. George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, U.K.

2. Wolfson Institute for Biomedical Research, The Rayne Institute, University College London, 5 University Street, London WC1E 6JJ, U.K.

3. Centre for Clinical Pharmacology, The Rayne Institute, University College London, 5 University Street, London WC1E 6JJ, U.K.

Abstract

Methylarginines inhibit nitric oxide synthases (NOS). Cellular concentrations of methylarginines are determined in part by the activity of dimethylarginine dimethylaminohydrolase (DDAH; EC 3.5.3.18). We have cloned human DDAH and identified and expressed a second novel DDAH isoform (DDAH I and II respectively). DDAH I predominates in tissues that express neuronal NOS. DDAH II predominates in tissues expressing endothelial NOS. These results strengthen the hypothesis that methylarginine concentration is actively regulated and identify molecular targets for the tissue and cell-specific regulation of methylarginine concentration.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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