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5号染色体长臂远端肾上腺素能和多巴胺受体基因与收缩压变异的连锁及关联

Linkage and association of adrenergic and dopamine receptor genes in the distal portion of the long arm of chromosome 5 with systolic blood pressure variation.

作者信息

Krushkal J, Xiong M, Ferrell R, Sing C F, Turner S T, Boerwinkle E

机构信息

Institute of Molecular Medicine and Human Genetics Center, The University of Texas-Houston Health Science Center, Houston, TX 77225, USA.

出版信息

Hum Mol Genet. 1998 Sep;7(9):1379-83. doi: 10.1093/hmg/7.9.1379.

DOI:10.1093/hmg/7.9.1379
PMID:9700190
Abstract

Elevated blood pressure is an important risk factor for renal-, cerebro- and cardiovascular diseases. We used an efficient discordant sib-pair ascertainment scheme to investigate the impact of the distal end of the long arm of human chromosome 5 (chromosomal region 5q31.1-qter) containing genes for the alpha1B and beta2 adrenergic receptors and the dopamine receptor type 1A on variation of systolic blood pressure in young Caucasians. We measured eight highly polymorphic markers spanning this positional candidate gene-rich region in 427 individuals from 55 three-generation pedigrees containing 69 discordant sibling pairs, and calculated multipoint identity by descent (MIBD) probabilities. The results of genetic linkage and association tests indicate that the region between markers D5S2093 and D5S462 is significantly linked to one or more polymorphic genes influencing interindividual variation in systolic blood pressure levels. Since the alpha1B adrenergic receptor and dopamine receptor type 1A genes are located close to these markers, these data suggest that genetic variation in one or both of these G protein-coupled receptors, which participate in the control of vascular tone, plays an important role in influencing interindividual variation in systolic blood pressure levels.

摘要

血压升高是肾脏、脑血管和心血管疾病的重要危险因素。我们采用了一种高效的不一致同胞对确定方案,来研究人类5号染色体长臂远端(染色体区域5q31.1-qter),该区域包含α1B和β2肾上腺素能受体以及1A型多巴胺受体的基因,对年轻白种人收缩压变异的影响。我们在来自55个三代家系的427名个体中测量了跨越这个富含位置候选基因区域的8个高度多态性标记,这些家系包含69对不一致的同胞对,并计算了多位点同源系数(MIBD)概率。遗传连锁和关联测试结果表明,标记D5S2093和D5S462之间的区域与一个或多个影响收缩压水平个体间变异的多态性基因显著连锁。由于α1B肾上腺素能受体和1A型多巴胺受体基因位于这些标记附近,这些数据表明,这两种参与血管张力控制的G蛋白偶联受体中的一种或两种的遗传变异,在影响收缩压水平个体间变异中起重要作用。

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