Functional Variant in microRNA-196a2 Contributes to the Susceptibility of Congenital Heart Disease in a Chinese Population

被引:120
作者
Xu, Jing [1 ]
Hu, Zhibin [2 ]
Xu, ZhengFeng [3 ]
Gu, Haiyong [1 ]
Yi, Long [4 ]
Cao, Hailong [1 ]
Chen, Jiaping [2 ]
Tian, Tian [2 ]
Liang, Jie [2 ]
Lin, Ying [3 ]
Qiu, Wanshan [5 ]
Ma, Hongxia [2 ]
Shen, Hongbing [2 ]
Chen, Yijiang [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Thorac & Cardiovasc Surg, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Nanjing 210029, Peoples R China
[3] Nanjing Med Univ, Affiliated Nanjing Matern & Child Hlth Hosp, Ctr Prenatal Diag, Nanjing 210029, Peoples R China
[4] Nanjing Univ, Sch Med, Dept Pathol, Nanjing 210008, Peoples R China
[5] Nanjing Med Univ, Affiliated Hosp 2, Dept Thorac & Cardiovasc Surg, Nanjing 210029, Peoples R China
基金
中国国家自然科学基金;
关键词
congenital heart disease; CHD; microRNA-196a2; VENTRICULAR SEPTAL-DEFECT; CARDIOVASCULAR DEFECTS; MUTATIONS; GENE; EXPRESSION; CARDIOGENESIS; ASSOCIATION; TARGETS; HOXB8; CELLS;
D O I
10.1002/humu.21044
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hox gene clusters play an important role during cardiac septation to valve formation in different species, and the miR-196a-HOXB8-Sonic hedgehog signaling pathway is of particular interest. Recently, we found that a genetic variant of rs11614913 in the miR-196a2 sequence could alter mature miR-196a expression and target mRNA binding; this observation led us to hypothesize that rs11614913 might influence susceptibility to sporadic congenital heart disease (CHD). We conducted a three-stage case-control study of CHD in Chinese to test our hypothesis by genotyping miR-196a2 rs11614913 and three other pre-miRNA SNPs (miR-146a rs2910164, miR-149 rs2292832, and miR-499 rs3746444) in 1,324 CHD cases and 1,783 non,CHD controls. We found that rs 11614913 CC was associated with a significantly increased risk of CHD in all three stages combined (P = 6.81 x 10(-6)). In a genotype-phenotype correlation analysis using 29 cardiac tissue samples of CHD, rs11614913 CC was associated with significantly increased mature miR-196a expression (P=0.001). In vitro binding assays further revealed that the rs 11614913 variant affects HOXB8 binding to mature miR-196a. This is the first study to indicate that miR-196a2 rs 11614913 plays a role in sporadic CHD susceptibility. Hum Mutat 30,1231-1236, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1231 / 1236
页数:6
相关论文
共 32 条
[11]   The microRNA Registry [J].
Griffiths-Jones, S .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D109-D111
[12]   The incidence of congenital heart disease [J].
Hoffman, JIE ;
Kaplan, S .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 39 (12) :1890-1900
[13]   The microRNA miR-196 acts upstream of Hoxb8 and Shh in limb development [J].
Hornstein, E ;
Mansfield, JH ;
Yekta, S ;
Hu, JKH ;
Harfe, BD ;
McManus, MT ;
Baskerville, S ;
Bartel, DP ;
Tabin, CJ .
NATURE, 2005, 438 (7068) :671-674
[14]   Genetic variants of miRNA sequences and non-small cell lung cancer survival [J].
Hu, Zhibin ;
Chen, Jiaping ;
Tian, Tian ;
Zhou, Xiaoyi ;
Gu, Haiyong ;
Xu, Lin ;
Zeng, Yi ;
Miao, Ruifen ;
Jin, Guangfu ;
Ma, Hongxia ;
Chen, Yijiang ;
Shen, Hongbing .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (07) :2600-2608
[15]   Noninherited risk factors and congenital cardiovascular defects: Current knowledge a scientific statement from the American Heart Association Council on cardiovascular disease in the young [J].
Jenkins, Kathy J. ;
Correa, Adolfo ;
Feinstein, Jeffrey A. ;
Botto, Lorenzo ;
Britt, Amy E. ;
Daniels, Stephen R. ;
Elixson, Marsha ;
Warnes, Carole A. ;
Webb, Catherine L. .
CIRCULATION, 2007, 115 (23) :2995-3014
[16]   HOX GENES IN VERTEBRATE DEVELOPMENT [J].
KRUMLAUF, R .
CELL, 1994, 78 (02) :191-201
[17]   Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice [J].
Lindsay, EA ;
Vitelli, F ;
Su, H ;
Morishima, M ;
Huynh, T ;
Pramparo, T ;
Jurecic, V ;
Ogunrinu, G ;
Sutherland, HF ;
Scambler, PJ ;
Bradley, A ;
Baldini, A .
NATURE, 2001, 410 (6824) :97-101
[18]   MicroRNA-responsive 'sensor' transgenes uncover Hox-like and other developmentally regulated patterns of vertebrate microRNA expression [J].
Mansfield, JH ;
Harfe, BD ;
Nissen, R ;
Obenauer, J ;
Srineel, J ;
Chaudhuri, A ;
Farzan-Kashani, R ;
Zuker, M ;
Pasquinelli, AE ;
Ruvkun, G ;
Sharp, PA ;
Tabin, CJ ;
McManus, MT .
NATURE GENETICS, 2004, 36 (10) :1079-1083
[19]   TBX1 is responsible for cardiovascular defects in Velo-Cardio-Facial/DiGeorge syndrome [J].
Merscher, S ;
Funke, B ;
Epstein, JA ;
Heyer, J ;
Puech, A ;
Lu, MM ;
Xavier, RJ ;
Demay, MB ;
Russell, RG ;
Factor, S ;
Tokooya, K ;
Jore, BS ;
Lopez, M ;
Pandita, RK ;
Lia, M ;
Carrion, D ;
Xu, H ;
Schorle, H ;
Kobler, JB ;
Scambler, P ;
Wynshaw-Boris, A ;
Skoultchi, AI ;
Morrow, BE ;
Kucherlapati, R .
CELL, 2001, 104 (04) :619-629
[20]   Steroid-dependent modification of Hox function drives myocyte reprogramming in the Drosophila heart [J].
Monier, B ;
Astier, M ;
Sémériva, M ;
Perrin, L .
DEVELOPMENT, 2005, 132 (23) :5283-5293