Association of connexin gene polymorphism with essential hypertension in Kazak and Han Chinese in Xinjiang, China

Li-jie Wang , Wen-wen Zhang , Liang Zhang , Wen-yan Shi , Ying-zi Wang , Ke-tao Ma , Wei-dong Liu , Lei Zhao , Li Li , Jun-qiang Si

Current Medical Science ›› 2017, Vol. 37 ›› Issue (2) : 197 -203.

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Current Medical Science ›› 2017, Vol. 37 ›› Issue (2) : 197 -203. DOI: 10.1007/s11596-017-1715-y
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Association of connexin gene polymorphism with essential hypertension in Kazak and Han Chinese in Xinjiang, China

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Abstract

Essential hypertension (EH) is affected by both genetic and environmental factors. The polymorphism of connexin (Cx) genes is found associated with the development of hypertension. However, the association of the polymorphism of Cxs with EH has not been investigated. This study aimed to investigate the association of the polymorphism of connexin (Cx) genes Cx37, Cx40, and Cx43 with EH in Kazak and Han Chinese in Xinjiang, China. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method and matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) were used to analyze the polymorphism of Cx genes in Kazak and Han EH patients as well as their normotensive controls. The results showed that there were no significant differences in the frequencies of different three genotypes (A/A, A/G, and G/G) and A and G alleles of Cx40 rs35594137 and rs11552588 between EH patients and normotensive controls. However, in Kazak EH patients, the frequencies of three genotypes (A/A, A/G, and G/G) of Cx37 rs1630310 were 24.8%, 47.2% and 28.0%, respectively, which were significantly different from those in Han EH patients. In Han EH patients, the frequencies of the three genotypes (C/C, C/G and G/G) of Cx43 rs1925223 were 6.4%, 35.6% and 58.0%, respectively. Frequencies of the other four genotypes had no statistical differences among Kazak and Han EH patients and their normotensive controls. These results suggest polymorphisms of Cx37 rs1630310 and Cx43 rs1925223 genes may be associated with the pathogenesis of EH. Carrying Cx37 rs1630310-A or Cx43 rs1925223-G genotypes may protect against the development of EH.

Keywords

essential hypertension / Kazak Chinese / Han Chinese / connexin genes / single nucleotide polymorphism

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Li-jie Wang, Wen-wen Zhang, Liang Zhang, Wen-yan Shi, Ying-zi Wang, Ke-tao Ma, Wei-dong Liu, Lei Zhao, Li Li, Jun-qiang Si. Association of connexin gene polymorphism with essential hypertension in Kazak and Han Chinese in Xinjiang, China. Current Medical Science, 2017, 37(2): 197-203 DOI:10.1007/s11596-017-1715-y

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References

[1]

AugustP. Initial treatment of hypertension. N Engl J Med, 2003, 348(7): 610-617 PMID: 12584370

[2]

MelanderO. Genetic factors in hypertension–what is known and what does it mean?. Blood Press, 2001, 10(5-6): 254-270 PMID: 11822531

[3]

PausovaZ, TremblayJ, HametP. Gene–environment interactions in hypertension. Curr Hypertens Rep, 1999, 1(1): 42-50 PMID: 10981041

[4]

LuftFC. Molecular genetics of human hypertension. J Hypertens, 1998, 16: 1871-1878 PMID: 9886871

[5]

ZhaoD, HuQH, DengFM, et al. . Aßsociation of the TGF-ß1 gene polymorphisms and blood TGF-ß1 level with essential hypertension in Kazakh Chinese. Chin J Med Genet, 2010, 27(4): 463-468

[6]

SeversNJ, RotheryS, DupontE, et al. . Immunocytochemical analysis of connexin expression in the healthy and diseased cardiovascular system. Microsc Res Tech, 2001, 52(3): 301-322 PMID: 11180622

[7]

MeseG, RichardG, WhiteTW. Gap junctions: basic structure and function. J Invest Dermatol, 2007, 127(11): 2516-2524 PMID: 17934503

[8]

RamR, WestcottAP, VerandasK, et al. . Mena associates and modulates connexin 43 remodeling in cardiomyocytes. Am J Physiol Heart Circ Physiol, 2014, 306(1): 154-159

[9]

LinJ, KeenerJP. Microdomain effects on transverse cardiac propagation. Biophys J, 2014, 106(4): 925-931 PMID: 24559995 PMCID: 3945098

[10]

SmythJW, ShawRM. Autoregulation of connexin43 gap junction formation by internally translated isoforms. Cell Rep, 2013, 5(3): 611-618 PMID: 24210816 PMCID: 3898934

[11]

ZhangSS, ShawRM. Trafficking highways to the intercalated disc: new insights unlocking the specificity of connexin43 localization. Cell Commun Aches, 2014, 21(1): 43-54

[12]

Looft-WilsonRC, BillaudM, JohnstonSR, et al. . Interaction between nitric oxide signaling and gap junctions: effects on vascular function. Biochem Biophys Acta, 2012, 1818(8): 1895-1902 PMID: 21835160

[13]

SimonAM, McWhorterAR. Vascular abnormalities in mice lacking the endothelial gap junction proteins connexin 37 and connexin 40. Dev Biol, 2002, 251(2): 206-220 PMID: 12435353

[14]

MaK-T, LiX-Z, LiL, et al. . Role of gap junctions in the contractile response to agonists in the mesenteric artery of spontaneously hypertensive rats. Hypertens Res, 2014, 37(2): 110-115 PMID: 24048484

[15]

CaiWJ, KocsisE, ScholzD, et al. . Presence of Cx37 and lack of desmin in smooth muscle cells are early markers for arteriogenesis. Mol Cell Biochem, 2004, 262(1): 17-23 PMID: 15532705

[16]

LeuHB, ChungCM, ChuangSY, et al. . Genetic variants of connexin 37 are associated with carotid intima-medial thickness and future onset of ischemic stroke. Atherosclerosis, 2011, 214(1): 101-106 PMID: 21044781

[17]

LairdDW. Life cycle of connexins in health and disease. Biochem J, 2006, 394: 527-543 PMID: 16492141 PMCID: 1383703

[18]

GraysonTH. Is Cx40 a marker for hypertension?. J Hypertens, 2006, 24(2): 279-280 PMID: 16508571

[19]

FirouziM, KokB, SpieringW, et al. . Polymorphisms in human connexin40 gene promoter are associated with increased risk of hypertension in men. J Hypertens, 2006, 24(2): 325-330 PMID: 16508580

[20]

LübkemeierI, MachuraK, KurtzL, et al. . The connexin40 A96S mutation causes rennin-dependent hypertension. J Am Soc Nephrol, 2011, 22(6): 1031-1040 PMID: 21597036 PMCID: 3103723

[21]

ChastonDJ, BaillieBK, GraysonTH, et al. . Polymorphism in endothelial connexin40 enhances sensitivity to intraluminal pressure and increases arterial stiffness. Arterioscler Thromb Vasc Biol, 2013, 33(5): 962-970 PMID: 23471232

[22]

GuoS, ChenW, YangY, et al. . Association between 1019C/T polymorphism in the connexin 37 gene and essential hypertension. Heart Lung Circ, 2014, 23(10): 924-929 PMID: 24685073

[23]

ChobanianAV, BakrisGL, BlackHR, et al. . The seventh report of the joint national committee on prevention, detection, evaluation, and treatment of high blood pressure: The JNC report. JAMA, 2003, 289(19): 2560-2572 PMID: 12748199

[24]

YuanL, MaW, LiuJ, et al. . Effects of GSTM1/GSTT1 gene polymorphism and fruit & vegetable consumption on antioxidant biomarkers and cognitive function in the elderly: A community based cross-sectional study. Plos One, 2014, 9(11): e113588 PMID: 25420021 PMCID: 4242636

[25]

WangJ, LiuS, WangB, et al. . Association between gout and polymorphisms in GCKR in male Han Chinese. Hum Genet, 2012, 131(7): 1261-1265 PMID: 22395765

[26]

GroenewegenWA, FirouziM, BezzinaCR, et al. . A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill. Circ Res, 2003, 92(1): 14-22 PMID: 12522116

[27]

FirouziM, RamannaH, KokB, et al. . Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation. Circ Res, 2004, 95(4): 29-33

[28]

KumarNM, GilulaNB. The gap junction communication channel. Cell, 1996, 84(3): 381-318 PMID: 8608591

[29]

RyanMJ, LiuB, HerbowyMT, et al. . Intercellular communication between renin expressing As4.1 cells, endothelial cells and smooth muscle cells. Life Sci, 2003, 72(11): 1289-1301 PMID: 12570929

[30]

MeensMJ, PfennigerA, KwakBR, et al. . Regulation of cardiovascular connexins by mechanical forces and junctions. Cardiovasc Res, 2013, 99(2): 304-314 PMID: 23612582 PMCID: 3695747

[31]

GollobMH, JonesDL, KrahnAD, et al. . Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation. N Engl J Med, 2006, 354(25): 2677-2688 PMID: 16790700

[32]

GemelJ, LevyAE, SimonAR, et al. . Connexin40 abnormalities and atrial fibrillation in the human heart. J Mol Cell Cardiol, 2014, 76: 159-168 PMID: 25200600

[33]

PfenniqerA w d, LaanSW, SanderW, et al. . Lack of association between connexin40 polymorphisms and coronary artery disease. Atherosclerosis, 2012, 222(1): 148-153

[34]

ZhangC, ZhengL. Distribution of Cx37 gene C1019T polymorphism in Cantonese Han nationality population of China. Laboratory Med, 2008, 23(5): 509-512

[35]

ListiF, CandoreG, BalistreriCR, et al. . Connexin 37(1019) gene polymorphism in myocardial infarction patients and centenarians. Atherosclerosis, 2007, 191(2): 460-461 PMID: 16970956

[36]

PithaJ, HubacekJA, PithovaP. The connexin 37(1019C>T) gene polymorphism is associated with subclinical atherosclerosis in women with type 1 and 2 diabetes and in women with central obesity. Physiol Res, 2010, 59(6): 1029-1032 PMID: 21208019

[37]

FengW, WangH, WangY. Relevance of connexin 37gene-C1019T polymorphism and coronary artery disease in han population in Anhui region. Chin J Cardiovasc Rehabil Med, 2010, 19(1): 33-36

[38]

WongCW, ChristenT, RothI, et al. . Connexin 37 protects against atherosclerosis by regulating monocyte adhesion. Nat Med, 2006, 12(8): 950-954 PMID: 16862155

[39]

GuoS, ChenW, YangY, et al. . Association between 1019C/T polymorphism in the connexin 37 gene and essential hypertensi. Heart Lung Circ, 2014, 23(10): 924-929 PMID: 24685073

[40]

TheiM, de WitC, SchlaegerTM, et al. . Endonthelium-specific replacement of the connexin 43 coding region by a lacZ reporter gene. Genesis, 2001, 29(1): 1-13

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