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加拿大奥吉-克里人的G蛋白β3亚基基因变异与血压变化

G protein beta3 subunit gene variant and blood pressure variation in Canadian Oji-Cree.

作者信息

Hegele R A, Harris S B, Hanley A J, Cao H, Zinman B

机构信息

Robarts Research Institute and Department of Medicine, Thames Valley Family Practice Research Unit, University of Western Ontario, London, Ontario, Canada.

出版信息

Hypertension. 1998 Oct;32(4):688-92. doi: 10.1161/01.hyp.32.4.688.

DOI:10.1161/01.hyp.32.4.688
PMID:9774364
Abstract

The subunits of the heterotrimeric G proteins are attractive candidate gene products for both susceptibility to essential hypertension and interindividual variation in blood pressure. There is alternative splicing of exon 9 of the gene encoding the beta3 subunit of heterotrimeric G proteins (GNB3) associated with a C-->T change at nucleotide 825, which activates a cryptic splice site. The 825T allele results in a gene product that is 41 amino acids smaller than the wild-type gene product. G protein heterotrimers containing the shorter variant are more reactive than those containing the wild type, and the 825T allele appears to be associated with essential hypertension. To evaluate whether this variant is associated with hypertension or blood pressure in other human samples, we genotyped 447 young adult Oji-Cree for the GNB3 C825T variation. We found that the frequency of the GNB3 825T allele was 0.501 in the Oji-Cree, which is considerably higher than the frequency observed in whites. Furthermore, genetic variation of the GNB3 nucleotide 825 was significantly associated with variation in systolic pressure but not diastolic pressure. Specifically, subjects with the 825T/T genotype had significantly lower systolic pressure than subjects with the 825C/T and 825C/C genotypes; the association was independent of sex. Furthermore, the 825T allele frequency tended to be higher in subjects who took antihypertensive medications than in subjects who did not (0.571 versus 0.496; P=NS), although this young sample had relatively few subjects with hypertension. The findings support an association of variation in this gene with variation in blood pressure.

摘要

异源三聚体G蛋白的亚基是原发性高血压易感性和个体间血压差异的有吸引力的候选基因产物。编码异源三聚体G蛋白β3亚基(GNB3)的基因外显子9存在选择性剪接,与核苷酸825处的C→T变化相关,该变化激活了一个隐蔽剪接位点。825T等位基因导致一种基因产物,其比野生型基因产物小41个氨基酸。含有较短变体的G蛋白异源三聚体比含有野生型的更具反应性,并且825T等位基因似乎与原发性高血压相关。为了评估该变体是否与其他人类样本中的高血压或血压相关,我们对447名年轻成年奥吉 - 克里人进行了GNB3 C825T变异的基因分型。我们发现,奥吉 - 克里人中GNB3 825T等位基因的频率为0.501,这明显高于在白人中观察到的频率。此外,GNB3核苷酸825的基因变异与收缩压变异显著相关,但与舒张压变异无关。具体而言,825T/T基因型的受试者收缩压明显低于825C/T和825C/C基因型的受试者;这种关联与性别无关。此外,服用抗高血压药物的受试者中825T等位基因频率往往高于未服用的受试者(0.571对0.496;P=无显著性差异),尽管这个年轻样本中患有高血压的受试者相对较少。这些发现支持该基因变异与血压变异之间的关联。

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