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Genetic Variation in Renal Expression of Folate Receptor 1 (Folr1) Gene Predisposes Spontaneously Hypertensive Rats to Metabolic Syndrome.

Abstract
Metabolism of homocysteine and other sulfur amino acids is closely associated with metabolism of folates. In this study, we analyzed the possible role of folates and sulfur amino acids in the development of features of the metabolic syndrome in the BXH/HXB recombinant inbred strains derived from the spontaneously hypertensive rat (SHR) and Brown Norway progenitors. We mapped a quantitative trait locus for cysteine concentrations to a region of chromosome 1 that contains a cis-acting expression quantitative trait locus regulating mRNA levels of folate receptor 1 (Folr1) in the kidney. Sequence analysis revealed a deletion variant in the Folr1 promoter region of the SHR. Transfection studies demonstrated that the SHR-promoter region of Folr1 is less effective in driving luciferase reporter gene expression than the Brown Norway promoter region of Folr1. Results in the SHR.BN-chr.1 congenic strain confirmed that the SHR variant in Folr1 cosegregates with markedly reduced renal expression of Folr1 and renal folate reabsorption, decreased serum levels of folate, increased serum levels of cysteine and homocysteine, increased adiposity, ectopic fat accumulation in liver and muscle, reduced muscle insulin sensitivity, and increased blood pressure. Transgenic rescue experiments performed by expressing a Folr1 transgene in the SHR ameliorated most of the metabolic disturbances. These findings are consistent with the hypothesis that inherited variation in the expression of Folr1 in the kidney influences the development of the metabolic syndrome and constitutes a previously unrecognized genetic mechanism that may contribute to increased risk for diabetes mellitus and cardiovascular disease.
AuthorsMichal Pravenec, Viktor Kožich, Jakub Krijt, Jitka Sokolová, Václav Zídek, Vladimír Landa, Petr Mlejnek, Jan Šilhavý, Miroslava Šimáková, Vojtěch Škop, Jaroslava Trnovská, Ludmila Kazdová, Takashi Kajiya, Jiaming Wang, Theodore W Kurtz
JournalHypertension (Dallas, Tex. : 1979) (Hypertension) Vol. 67 Issue 2 Pg. 335-41 (Feb 2016) ISSN: 1524-4563 [Electronic] United States
PMID26667416 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2015 American Heart Association, Inc.
Chemical References
  • Folate Receptor 1
  • RNA
Topics
  • Animals
  • Blood Pressure (physiology)
  • Folate Receptor 1 (biosynthesis, genetics)
  • Gene Expression Regulation
  • Genetic Predisposition to Disease
  • Genetic Variation
  • Hypertension (complications, genetics, metabolism)
  • Kidney (metabolism)
  • Male
  • Metabolic Syndrome (etiology, genetics, metabolism)
  • RNA (genetics)
  • Rats
  • Rats, Inbred BN
  • Rats, Inbred SHR
  • Real-Time Polymerase Chain Reaction

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