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
[1]   Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome [J].
Basson, CT ;
Bachinsky, DR ;
Lin, RC ;
Levi, T ;
Elkins, JA ;
Soults, J ;
Grayzel, D ;
Kroumpouzou, E ;
Traill, TA ;
LeblancStraceski, J ;
Renault, B ;
Kucherlapati, R ;
Seidman, JG ;
Seidman, CE .
NATURE GENETICS, 1997, 15 (01) :30-35
[2]   The developmental genetics of congenital heart disease [J].
Bruneau, Benoit G. .
NATURE, 2008, 451 (7181) :943-948
[3]   EXPRESSION OF HOMEOBOX GENES MSX-1 (HOX-7) AND MSX-2 (HOX-8) DURING CARDIAC DEVELOPMENT IN THE CHICK [J].
CHANTHOMAS, PS ;
THOMPSON, RP ;
ROBERT, B ;
YACOUB, MH ;
BARTON, PJR .
DEVELOPMENTAL DYNAMICS, 1993, 197 (03) :203-216
[4]   REGIONALLY RESTRICTED DEVELOPMENTAL DEFECTS RESULTING FROM TARGETED DISRUPTION OF THE MOUSE HOMEOBOX GENE HOX-1.5 [J].
CHISAKA, O ;
CAPECCHI, MR .
NATURE, 1991, 350 (6318) :473-479
[5]   GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5 [J].
Garg, V ;
Kathiriyra, IS ;
Barnes, R ;
Schluterman, MK ;
King, IN ;
Butler, CA ;
Rothrock, CR ;
Eapen, RS ;
Hirayama-Yamada, K ;
Joo, K ;
Matsuoka, R ;
Cohen, JC ;
Srivastava, D .
NATURE, 2003, 424 (6947) :443-447
[6]   An SNP-guided microRNA map of fifteen common human disorders identifies a consensus disease phenocode aiming at principal components of the nuclear import pathway [J].
Glinsky, Gennadi V. .
CELL CYCLE, 2008, 7 (16) :2570-2583
[7]   Intracardiac septation requires hedgehog-dependent cellular contributions from outside the heart [J].
Goddeeris, Matthew M. ;
Rho, Silvia ;
Petiet, Alexandra ;
Davenport, Chandra L. ;
Johnson, G. Allan ;
Meyers, Erik N. ;
Klingensmith, John .
DEVELOPMENT, 2008, 135 (10) :1887-1895
[8]   Independent requirements for Hedgehog signaling by both the anterior heart field and neural crest cells for outflow tract development [J].
Goddeeris, Matthew M. ;
Schwartz, Robert ;
Klingensmith, John ;
Meyers, Erik N. .
DEVELOPMENT, 2007, 134 (08) :1593-1604
[9]  
Gong Li-guo, 2005, Zhonghua Yixue Yichuanxue Zazhi, V22, P497
[10]   Congenital abnormalities of body patterning: embryology revisited [J].
Goodman, FR .
LANCET, 2003, 362 (9384) :651-662