Msx1 and Msx2 are functional interacting partners of T-box factors in the regulation of Connexin43

被引:65
作者
Boogerd, Kees-Jan [1 ]
Wong, L. Y. Elaine [1 ]
Christoffels, Vincent M. [1 ]
Klarenbeek, Meinke [1 ]
Ruijter, Jan M. [1 ]
Moorman, Antoon F. M. [1 ]
Barnett, Phil [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Heart Failure Res Ctr, Dept Anat & Embryol, NL-1105 AZ Amsterdam, Netherlands
关键词
T-box transcription factor; heart development; Tbx2; Tbx3; Msx1; Msx2; Connexin43; atrioventricutar canal; working myocardium; cardiac conduction system; mouse; chicken;
D O I
10.1093/cvr/cvn049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims T-box factors Tbx2 and Tbx3 play key roles in the development of the cardiac conduction system, atrioventricular canal, and outflow tract of the heart. They regulate the gap-junction-encoding gene Connexin43 (Cx43) and other genes critical for heart development and function. Discovering protein partners of Tbx2 and Tbx3 wilt shed light on the mechanisms by which these factors regulate these gene programs. Methods and results Employing an yeast 2-hybrid screen and subsequent in vitro pull-down experiments we demonstrate that muscle segment homeobox genes Msx1 and Msx2 are able to bind the cardiac T-box proteins Tbx2, Tbx3, and Tbx5. This interaction, as that of the related Nkx2.5 protein, is supported by the T-box and homeodomain alone. Overlapping spatiotemporal expression patterns of Msx1 and Msx2 together with the T-box genes during cardiac development in mouse and chicken underscore the biological significance of this interaction. We demonstrate that Msx proteins together with Tbx2 and Tbx3 suppress Cx43 promoter activity and down regulate Cx43 gene activity in a rat heart-derived cell line. Using chromatin immunoprecipitation analysis we demonstrate that Msx1 can bind the Cx43 promoter at a conserved binding site located in close proximity to a previously defined T-box binding site, and that the activity of Msx proteins on this promoter appears dependent in the presence of Tbx3. Conclusion Msx1 and Msx2 can function in concert with the T-box proteins to suppress Cx43 and other working myocardial genes.
引用
收藏
页码:485 / 493
页数:9
相关论文
共 46 条
[1]   Overlapping and differential localization of Bmp-2, Bmp-4, Msx-2 and apoptosis in the endocardial cushion and adjacent tissues of the developing mouse heart [J].
Abdelwahid, E ;
Rice, D ;
Pelliniemi, LJ ;
Jokinen, E .
CELL AND TISSUE RESEARCH, 2001, 305 (01) :67-78
[2]   Msx homeobox gene family and craniofacial development [J].
Alappat, S ;
Zhang, ZY ;
Chen, YP .
CELL RESEARCH, 2003, 13 (06) :429-442
[3]   The peroxisomal membrane protein Pex13p shows a novel mode of SH3 interaction [J].
Barnett, P ;
Bottger, G ;
Klein, ATJ ;
Tabak, HF ;
Distel, B .
EMBO JOURNAL, 2000, 19 (23) :6382-6391
[4]   Tension-induced reduction in connexin 43 expression in cranial sutures is linked to transcriptional regulation by TBX2 [J].
Borke, JL ;
Yu, JC ;
Isales, CM ;
Wagle, N ;
Do, NN ;
Chen, JR ;
Bollag, RJ .
ANNALS OF PLASTIC SURGERY, 2003, 51 (05) :499-504
[5]  
Borke JL, 2003, CLEFT PALATE-CRAN J, V40, P284, DOI 10.1597/1545-1569(2003)040<0284:NTROCB>2.0.CO
[6]  
2
[7]   A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease [J].
Bruneau, BG ;
Nemer, G ;
Schmitt, JP ;
Charron, F ;
Robitaille, L ;
Caron, S ;
Conner, DA ;
Gessler, M ;
Nemer, M ;
Seidman, CE ;
Seidman, JG .
CELL, 2001, 106 (06) :709-721
[8]   NUCLEOTIDES FLANKING A CONSERVED TAAT CORE DICTATE THE DNA-BINDING SPECIFICITY OF 3 MURINE HOMEODOMAIN PROTEINS [J].
CATRON, KM ;
ILER, N ;
ABATE, C .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) :2354-2365
[9]   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
[10]   Tbx2 represses expression of Connexin43 in osteoblastic-like cells [J].
Chen, JR ;
Chatterjee, B ;
Meyer, R ;
Yu, JC ;
Borke, JL ;
Isales, CM ;
Kirby, ML ;
Lo, CW ;
Bollag, RJ .
CALCIFIED TISSUE INTERNATIONAL, 2004, 74 (06) :561-573