TY - JOUR
T1 - Decreased transcriptional activity of calcium-sensing receptor gene promoter 1 is associated with calcium nephrolithiasis
AU - GENIAL network
AU - Vezzoli, Giuseppe
AU - Terranegra, Annalisa
AU - Aloia, Andrea
AU - Arcidiacono, Teresa
AU - Milanesi, Luciano
AU - Mosca, Ettore
AU - Mingione, Alessandra
AU - Spotti, Donatella
AU - Cusi, Daniele
AU - Hou, Jianghui
AU - Hendy, Geoffrey N.
AU - Soldati, Laura
PY - 2013
Y1 - 2013
N2 - Background: CaSR gene is a candidate for calcium nephrolithiasis. Single-nucleotide polymorphisms (SNPs) encompassing its regulatory region were associated with calcium nephrolithiasis. Aims: We tested SNPs in the CaSR gene regulatory region associated with calcium nephrolithiasis and their effects in kidney. Subjects and Methods: One hundred sixty-seven idiopathic calcium stone formers and 214 healthy controls were genotyped for four CaSR gene SNPs identified by bioinformatics analysis as modifying transcription factor binding sites. Strontium excretion afteranoral loadwastested in 55 stone formers. Transcriptional activity induced by variant alleles at CaSR gene promoters was compared by luciferase reporter gene assay in HEK-293 and HKC-8 cells. CaSR and claudin-14 mRNA levels were measured by real-Time PCR in 107 normal kidney medulla samples and compared in patients with different CaSR genotype. Results: Only rs6776158 (A>G), located in the promoter 1, was associated with nephrolithiasis. Its minor G allele was more frequent in stone formers than controls (37.8% vs 26.4%, P = .001). A reduced strontium excretion was observed in GG homozygous stone formers. Luciferase fluorescent activity was lower in cells transfected with the promoter 1 including G allele at rs6776158 than cells transfected with the A allele. CaSRmRNAlevels were lower in kidney medulla samples from homozygous carriers for theGallele at rs6776158 than carriers for the A allele. Claudin-14 mRNA levels were also lower in GG homozygous subjects. Conclusions: Minor allele at rs6776158 may predispose to calcium stones by decreasing transcriptional activity of theCaSRgenepromoter 1andCaSRexpression in kidney tubules.
AB - Background: CaSR gene is a candidate for calcium nephrolithiasis. Single-nucleotide polymorphisms (SNPs) encompassing its regulatory region were associated with calcium nephrolithiasis. Aims: We tested SNPs in the CaSR gene regulatory region associated with calcium nephrolithiasis and their effects in kidney. Subjects and Methods: One hundred sixty-seven idiopathic calcium stone formers and 214 healthy controls were genotyped for four CaSR gene SNPs identified by bioinformatics analysis as modifying transcription factor binding sites. Strontium excretion afteranoral loadwastested in 55 stone formers. Transcriptional activity induced by variant alleles at CaSR gene promoters was compared by luciferase reporter gene assay in HEK-293 and HKC-8 cells. CaSR and claudin-14 mRNA levels were measured by real-Time PCR in 107 normal kidney medulla samples and compared in patients with different CaSR genotype. Results: Only rs6776158 (A>G), located in the promoter 1, was associated with nephrolithiasis. Its minor G allele was more frequent in stone formers than controls (37.8% vs 26.4%, P = .001). A reduced strontium excretion was observed in GG homozygous stone formers. Luciferase fluorescent activity was lower in cells transfected with the promoter 1 including G allele at rs6776158 than cells transfected with the A allele. CaSRmRNAlevels were lower in kidney medulla samples from homozygous carriers for theGallele at rs6776158 than carriers for the A allele. Claudin-14 mRNA levels were also lower in GG homozygous subjects. Conclusions: Minor allele at rs6776158 may predispose to calcium stones by decreasing transcriptional activity of theCaSRgenepromoter 1andCaSRexpression in kidney tubules.
UR - https://www.scopus.com/pages/publications/84883724024
U2 - 10.1210/jc.2013-1834
DO - 10.1210/jc.2013-1834
M3 - Article
C2 - 23864702
AN - SCOPUS:84883724024
SN - 0021-972X
VL - 98
SP - 3839
EP - 3847
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 9
ER -