Identification of a novel polymorphism in the 3'UTR of the L-arginine transporter gene SLC7A1: contribution to hypertension and endothelial dysfunction

Circulation. 2007 Mar 13;115(10):1269-74. doi: 10.1161/CIRCULATIONAHA.106.665836. Epub 2007 Feb 26.

Abstract

Background: Endothelial dysfunction because of reduced nitric oxide bioavailability is a key feature of essential hypertension. We have found that normotensive siblings of subjects with essential hypertension have impaired endothelial function accompanied by altered arginine metabolism.

Methods and results: We have identified a novel C/T polymorphism in the 3'UTR of the principal arginine transporter, solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 gene (SLC7A1). The minor T allele significantly attenuates reporter gene expression (P<0.01) and is impaired in its capacity to form DNA-protein complexes (P<0.05). In 278 hypertensive subjects the frequency of the T allele was 13.3% compared with 7.6% in 498 normotensive subjects (P<0.001). Moreover, the overall genotype distribution observed in hypertensives differed significantly from that in normotensives (P<0.001). To complement these studies, we generated an endothelial-specific transgenic mouse overexpressing L-arginine transporter SLC7A1. The Slc7A1 transgenic mice exhibited significantly enhanced responses to the endothelium-dependent vasodilator acetylcholine (-log EC50 for wild-type versus Slc7A1 transgenic: 6.87+/-0.10 versus 7.56+/-0.13; P<0.001). This was accompanied by elevated production of nitric oxide by isolated aortic endothelial cells.

Conclusions: The present study identifies a key, functionally active polymorphism in the 3'UTR of SLC7A1. As such, this polymorphism may account for the apparent link between altered endothelial function, L-arginine, and nitric oxide metabolism and predisposition to essential hypertension.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Flanking Region / genetics*
  • Animals
  • Aorta / drug effects
  • Aorta / physiopathology
  • Arginine / metabolism
  • CHO Cells
  • Cationic Amino Acid Transporter 1 / genetics*
  • Cells, Cultured
  • Cricetinae
  • Cricetulus
  • Electrophoretic Mobility Shift Assay
  • Endothelial Cells / metabolism*
  • Gene Frequency
  • Gene Transfer Techniques
  • Genes, Reporter
  • Genotype
  • HeLa Cells
  • Humans
  • Hypertension / genetics*
  • Mice
  • Nitric Oxide
  • Organ Culture Techniques
  • Polymorphism, Genetic*
  • Vasodilation / drug effects
  • Vasodilation / genetics
  • Vasodilator Agents / pharmacology

Substances

  • Cationic Amino Acid Transporter 1
  • SLC7A1 protein, human
  • Vasodilator Agents
  • Nitric Oxide
  • Arginine