- VernacularTitle:CACNB2基因多态性与原发性高血压的关联性研究
- Author:
Qian SUN
1
;
Xin WANG
;
Ying HUANG
;
Yunliang HU
;
Jifei TANG
;
Yan LIN
;
Yuxin NIU
;
Xiaoou WANG
;
Bing DU
Author Information
- Publication Type:Journal Article
- MeSH: Aged; Alleles; Base Sequence; Calcium Channels, L-Type; genetics; Case-Control Studies; Cell Line; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Hypertension; genetics; Male; Middle Aged; Polymorphism, Single Nucleotide
- From: Chinese Journal of Medical Genetics 2013;30(3):340-344
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo assess the association between single nucleotide polymorphisms (SNPs) of calcium channel β 2 subunit (CACNB2) gene and essential hypertension (EH) in ethnic Han Chinese in Wenzhou area, and to study the influence of rs7069292 alleles on gene expression with luciferase reporter technique.
METHODSSixty hundred and thirty seven Han Chinese with EH and 600 normal controls were enrolled. Genotypes of 6 SNP within CACNB2 gene including rs2228645, rs2357928, rs7069292, rs7099380, rs10764319 and rs11014166 were determined with matrix assisted laser desorption ionization/time of flight mass spectrometer (MALDI-TOF MS). A luciferase reporter gene plasmid containing the fragment flanking rs7069292 (-2831 bp to -2460 bp) in the 5' regulatory region of CACNB2 was constructed.
RESULTSCompared with the control, CT and TT genotypes for the rs7069292 locus were significantly more common in EH group (5.20% vs. 2.17%, 2.59% vs. 1.08%, P< 0.05). CC genotype was not found. Promoter activity for allele C of the rs7069292 locus was significantly increased compared with allele T (P< 0.05). No significant difference was detected for other 5 SNPs in terms of genotypes and allele frequency.
CONCLUSIONThe rs7069292 CT polymorphism of the CACNB2 gene is associated with EH in ethnic Han Chinese from Wenzhou area. A T>C mutation may affect the expression of CACNB2.