Differential regulation of Tbx5 protein expression and sub-cellular localization during heart development

被引:31
作者
Bimber, Benjamin
Dettman, Robert W.
Simon, Hans-Georg
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Pediat, CMRC, Chicago, IL 60614 USA
[2] Northwestern Univ, Feinberg Cardiovasc Res Inst, Chicago, IL 60611 USA
关键词
Tbx5; LMP4; myocardium; epicardium; coronary artery; cardiac myocyte; cytoskeleton; heart development;
D O I
10.1016/j.ydbio.2006.09.023
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The T-box transcription factor Tbx5 can interact with Nkx2.5 and Gata4 transcription factors to synergistically regulate heart-specific genes in the nucleus. While a nuclear role for Tbx5 is clearly defined, we have previously shown that Tbx5 shuttles from nuclear to cytoplasmic sites, forming a complex with the PDZ-LIM protein LMP4 on the actin cytoskeleton. In this study, using a developmental series of chicken hearts, we provide the first evidence for differential Tbx5 protein expression and sub-cellular localization during cardiogenesis. At the tissue level, we show temporally and spatially restricted Tbx5 co-expression with LMP4. In cells co-expressing LMP4 and Tbx5 we demonstrate dynamic Tbx5 relocalization from exclusively nuclear to nuclear and cytoplasmic expression in the atrio-ventricular cushion. Furthermore, in coronary vessel development we show exclusive cytoplasmic localization of Tbx5, indicating a function for Tbx5 in the cytoplasm. In addition, we discover unknown regulation of Tbx5 and LMP4 expression in epicardial tissue, suggesting a specific role for Tbx5 in epicardial formation. These studies provide in vivo significance of the LMP4/Tbx5 protein interaction, suggesting both nuclear and cytoplasmic roles for Tbx5. The shuttling between nuclear and cytoplasmic sites reveals a novel mechanism for Tbx transcription factor regulation in chicken heart development allowing new insights for a better understanding of the molecular basis of hand/heart birth defects associated with TBX5 mutations. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:230 / 242
页数:13
相关论文
共 41 条
[1]   Tbx5 is essential for forelimb bud initiation following patterning of the limb field in the mouse embryo [J].
Agarwal, P ;
Wylie, JN ;
Galceran, J ;
Arkhitko, O ;
Li, CL ;
Deng, CX ;
Grosschedl, R ;
Bruneau, BG .
DEVELOPMENT, 2003, 130 (03) :623-633
[2]   Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations [J].
Basson, CT ;
Huang, TS ;
Lin, RC ;
Bachinsky, DR ;
Weremowicz, S ;
Vaglio, A ;
Bruzzone, R ;
Quadrelli, R ;
Lerone, M ;
Romeo, G ;
Silengo, M ;
Pereira, A ;
Krieger, J ;
Mesquita, SF ;
Kamisago, M ;
Morton, CC ;
Pierpont, MEM ;
Müller, CW ;
Seidman, JG ;
Seidman, CE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :2919-2924
[3]   Developmental regulation of Tbx5 in zebrafish embryogenesis [J].
Begemann, G ;
Ingham, PW .
MECHANISMS OF DEVELOPMENT, 2000, 90 (02) :299-304
[4]  
BRASSINGTON AE, 2003, AM J HUM, V73
[5]   Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome [J].
Bruneau, BG ;
Logan, M ;
Davis, N ;
Levi, T ;
Tabin, CJ ;
Seidman, JG ;
Seidman, CE .
DEVELOPMENTAL BIOLOGY, 1999, 211 (01) :100-108
[6]   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
[7]   LMP4 regulates Tbx5 protein subcellular localization and activity [J].
Camarata, Troy ;
Bimber, Benjamin ;
Kulisz, Andre ;
Chew, Teng-Leong ;
Yeung, Jennifer ;
Simon, Hans-Georg .
JOURNAL OF CELL BIOLOGY, 2006, 174 (03) :339-348
[8]   THE CONTRIBUTION OF THE INFERIOR ENDOCARDIAL CUSHION OF THE ATRIOVENTRICULAR-CANAL TO CARDIAC SEPTATION AND TO THE DEVELOPMENT OF THE ATRIOVENTRICULAR VALVES - STUDY IN THE CHICK-EMBRYO [J].
DELACRUZ, MV ;
GIMENEZRIBOTTA, M ;
SARAVALLI, O ;
CAYRE, R .
AMERICAN JOURNAL OF ANATOMY, 1983, 166 (01) :63-72
[9]   Common epicardial origin of coronary vascular smooth muscle, perivascular fibroblasts, and intermyocardial fibroblasts in the avian heart [J].
Dettman, RW ;
Denetclaw, W ;
Ordahl, CP ;
Bristow, J .
DEVELOPMENTAL BIOLOGY, 1998, 193 (02) :169-181
[10]   Epicardial outgrowth inhibition leads to compensatory mesothelial outflow tract collar and abnormal cardiac septation and coronary formation [J].
Gittenberger-de Groot, AC ;
Peeters, MPFMV ;
Bergwerff, M ;
Mentink, MMT ;
Poelmann, RE .
CIRCULATION RESEARCH, 2000, 87 (11) :969-971