Title of article :
The Effect of Aspartate-Lysine-Isoleucine and Aspartate-Arginine-Tyrosine Mutations on the Expression and Activity of Vasopressin V2 Receptor Gene
Author/Authors :
Najafzadeh, Hossein shahid chamran university of ahvaz - School of Veterinary Medicine - Dept of Pharmacology and Toxicology, اهواز, ايران , Safaeian, Leila isfahan university of medical sciences - School of Pharmacy and Pharmaceutical Sciences - Dept of Pharmacology and Toxicology, اصفهان, ايران , Sadeghi, Hamid Mirmohammad isfahan university of medical sciences - School of Pharmacy and Pharmaceutical Sciences - Dept of Pharmacology and Toxicology, اصفهان, ايران , Rabbani, Mohammad isfahan university of medical sciences - School of Pharmacy and Pharmaceutical Sciences - Dept of Pharmacology and Toxicology, اصفهان, ايران , Jafarian, Abbas isfahan university of medical sciences - Isfahan Pharmaceutical Sciences Research Center - School of Pharmacy and Pharmaceutical Sciences, اصفهان, ايران
From page :
17
To page :
22
Abstract :
Vasopressin type 2 receptor (V2R) plays an important role in the water reabsorption in thekidney collecting ducts. V2R is a G protein coupled receptor (GPCR) and the triplet of amino acids aspartatearginine- histidine (DRH) in this receptor might significantly influence its activity similar to other GPCR.However, the role of this motif has not been fully confirmed. Therefore, the present study attempted to shed some more light on the role of DRH motif in G protein coupling and V2R function with the use of sitedirected mutagenesis. Methods: Nested PCR using specific primers was used to produce DNA fragmentscontaining aspartate-lysine-isoleucine and aspartate-arginine-tyrosine mutations with replacements of the arginine to lysine and histidine to tyrosine, respectively. After digestion, these inserts were ligated into the pcDNA3 vector and transformation into E. coli HB101 was performed using heat shock method. The obtained colonies were analyzed for the presence and orientation of the inserts using proper restriction enzymes. After transient transfection of COS-7 cells using diethylaminoethyl-dextran method, the adenylyl cyclase activity assay was performed for functional study. The cell surface expression was analyzed by indirect ELISAmethod. Results: The functional assay indicated that none of these mutations significantly altered cAMP production and cell surface expression of V2R in these cells. Conclusion: Since some substitutions in arginine residue have shown to lead to the inactive V2 receptor, further studies are required to define the role of this residue more precisely. However, it seems that the role of the histidine residue is not critical in the V2receptor function. Iran. Biomed. J. 14 (1 2): 17-22, 2010
Keywords :
Mutation , Polymerase chain reaction , Vasopressin receptor
Journal title :
Iranian Biomedical Journal(IBJ)
Journal title :
Iranian Biomedical Journal(IBJ)
Record number :
2567393
Link To Document :
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