Usami Satoru, Kishimoto Ichiro, Saito Yoshihiko, Harada Masaki, Kuwahara Koichiro, Nakagawa Yasuaki, Nakanishi Michio, Yasuno Shinji, Kangawa Kenji, Nakao Kazuwa
Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Japan.
Hypertens Res. 2008 Jan;31(1):89-96. doi: 10.1291/hypres.31.89.
Guanylyl cyclase (GC)-A (natriuretic peptide receptor [NPR]-1), the receptor for atrial and brain natriuretic peptide, is important in the regulation of blood pressure in animal models and, possibly, in humans. In this study, we examined the association between dinucleotide repeat polymorphism within the 5'-flanking region of the GC-A gene and essential hypertension in a group of Japanese subjects. By genotyping 177 hypertensive and 170 normotensive subjects, we identified 5 allele types with 6, 9, 10, 11 and 12 CT dinucleotide repeats, respectively, around position -293, upstream of the ATG codon in the human GC-A gene. The frequency of the (CT)n=6 allele was significantly higher among hypertensive than normotensive subjects, while the frequencies of the other allele types did not differ between the two groups. We also examined the linkage between G/A polymorphism at position -77 (rs13306004), downstream of the (CT)n polymorphism, and found that the (CT)n=6 allele was tightly linked to an A at position -77, while all other (CT)n alleles were linked to G. Promoter-reporter analyses carried out in cultured human aortic smooth muscle cells using a luciferase gene fused to the 5'-flanking region of the GC-A gene revealed that the promoter containing (CT)n=6 drove less transcriptional activity than that containing (CT)n=10. Finally, site-directed mutation showed that the (CT)n and G/A polymorphisms act synergistically to affect GC-A promoter activity. Our results thus define the (CT)n polymorphism in the 5'-flanking region of the GC-A gene as a potent and novel susceptibility marker for hypertension.
鸟苷酸环化酶(GC)-A(利钠肽受体[NPR]-1)是心房钠尿肽和脑钠尿肽的受体,在动物模型以及可能在人类的血压调节中起重要作用。在本研究中,我们检测了一组日本受试者中GC-A基因5'侧翼区域内二核苷酸重复多态性与原发性高血压之间的关联。通过对177名高血压患者和170名血压正常者进行基因分型,我们在人类GC-A基因ATG密码子上游约-293位置处分别鉴定出5种等位基因类型,其CT二核苷酸重复次数分别为6、9、10、11和12次。高血压患者中(CT)n = 6等位基因的频率显著高于血压正常者,而其他等位基因类型在两组之间的频率没有差异。我们还检测了(CT)n多态性下游-77位置处的G/A多态性(rs13306004)之间的连锁关系,发现(CT)n = 6等位基因与-77位置处的A紧密连锁,而所有其他(CT)n等位基因与G连锁。在培养的人主动脉平滑肌细胞中使用与GC-A基因5'侧翼区域融合的荧光素酶基因进行启动子-报告基因分析,结果显示含有(CT)n = 6的启动子驱动的转录活性低于含有(CT)n = 10的启动子。最后,定点突变表明(CT)n和G/A多态性协同作用影响GC-A启动子活性。因此,我们的结果将GC-A基因5'侧翼区域的(CT)n多态性定义为一种强大且新的高血压易感性标志物。