Much has been learned about the molecular mechanisms that regulate the differentiation of the skeletal muscle lineages during mammalian development. In contrast, relatively little is currently understood about molecular bases of cardiac myocyte differentiation. Recent studies have demonstrated that distinct transcriptional pathways regulate skeletal and cardiac- specific gene expression and differentiation. However, until recently, the identity of the important transcription factors that regulate cardiac-specific gene expression have remained unclear. Members of the GATA family of zinc finger transcription factors have been shown to play important roles in the differentiation of multiple hematopoietic lineages. Recent evidence from the applicant and others suggests an important role for a new member of this family, GATA-4, in the coordinate regulation of cardiac-specific gene expression during heart development. GATA-4 expression is restricted to the pre-cardiac mesoderm and folding heart tube in the early mouse embryo. Moreover, GATA-4 expression precedes that of the cardiac contractile proteins by 0.5-1 day during mouse embryogenesis. Most importantly, GATA-4 binds to the promoter-enhancer elements of multiple cardiac genes, including the cardiac troponin C and troponin T genes, the ANF gene, the myosin light chain 1 gene, and the alpha-MHC gene. In addition, the forced expression of GATA-4 can directly transactivate the expression of at least some of these cardiac- specific promoter-enhancers in non-muscle cells. Taken together, these studies are consistent with the hypothesis that GATA-4 is one of the important cardiac myocyte determining genes. The studies described in this application are intended to (i) map the important functional domains of the GATA-4 transcription factor, (ii) directly test the role of GATA-4 in the regulation of cardiac gene expression and cardiac myocyte differentiation by studying the effects of targeted disruptions of the GATA-4 gene on cardiac myocyte development in vitro and in vivo, and (iii) map the regions of GATA-4 that are necessary for cardiac myocyte differentiation and gene expression during the in vitro differentiation of ES cells into embryoid bodies.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL054592-01
Application #
2232978
Study Section
Cardiovascular and Pulmonary Research A Study Section (CVA)
Project Start
1995-09-25
Project End
1999-08-31
Budget Start
1995-09-25
Budget End
1996-08-31
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Watson, Peter A; Birdsey, Nicholas; Huggins, Gordon S et al. (2010) Cardiac-specific overexpression of dominant-negative CREB leads to increased mortality and mitochondrial dysfunction in female mice. Am J Physiol Heart Circ Physiol 299:H2056-68
Gupta, Amitabh; Hou, Rong; Liu, Liming et al. (2009) Daxx inhibits muscle differentiation by repressing E2A-mediated transcription. J Cell Biochem 107:438-47
Dean, Jarrod; Plante, Jeremy; Huggins, Gordon S et al. (2009) Role of cyclic AMP-dependent kinase response element-binding protein in recombinant adeno-associated virus-mediated transduction of heart muscle cells. Hum Gene Ther 20:1005-12
Aikawa, Ryuichi; Huggins, Gordon S; Snyder, Richard O (2002) Cardiomyocyte-specific gene expression following recombinant adeno-associated viral vector transduction. J Biol Chem 277:18979-85
Huggins, G S; Bacani, C J; Boltax, J et al. (2001) Friend of GATA 2 physically interacts with chicken ovalbumin upstream promoter-TF2 (COUP-TF2) and COUP-TF3 and represses COUP-TF2-dependent activation of the atrial natriuretic factor promoter. J Biol Chem 276:28029-36
Fentzke, R C; Korcarz, C E; Shroff, S G et al. (2001) The left ventricular stress-velocity relation in transgenic mice expressing a dominant negative CREB transgene in the heart. J Am Soc Echocardiogr 14:209-18
Svensson, E C; Huggins, G S; Lin, H et al. (2000) A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding Fog-2. Nat Genet 25:353-6
Svensson, E C; Huggins, G S; Dardik, F B et al. (2000) A functionally conserved N-terminal domain of the friend of GATA-2 (FOG-2) protein represses GATA4-dependent transcription. J Biol Chem 275:20762-9
Arteaga, G M; Palmiter, K A; Leiden, J M et al. (2000) Attenuation of length dependence of calcium activation in myofilaments of transgenic mouse hearts expressing slow skeletal troponin I. J Physiol 526 Pt 3:541-9
Svensson, E C; Tufts, R L; Polk, C E et al. (1999) Molecular cloning of FOG-2: a modulator of transcription factor GATA-4 in cardiomyocytes. Proc Natl Acad Sci U S A 96:956-61

Showing the most recent 10 out of 19 publications