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

Developmental Biology

Volumn 302, Issue 1, 2007, Pages 230-242

  Bimber, Benjamin ^a   Dettman, Robert W ^a   Simon, Hans Georg ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Cardiac myocyte; Coronary artery; Cytoskeleton; Epicardium; Heart development; LMP4; Myocardium; Tbx5

Indexed keywords

ACTIN; CYTOSKELETON PROTEIN; LIM PROTEIN; MUTANT PROTEIN; NUCLEAR PROTEIN; PDZ PROTEIN; PROTEIN LMP4; TRANSCRIPTION FACTOR GATA 4; TRANSCRIPTION FACTOR NKX2.5; TRANSCRIPTION FACTOR TBX5; UNCLASSIFIED DRUG;

ANGIOGENESIS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BIRTH DEFECT; CELL NUCLEUS; CHICKEN; CORONARY BLOOD VESSEL; CYTOPLASM; CYTOSKELETON; EMBRYO; FUNCTIONAL PROTEOMICS; GENE CONTROL; HEART DEVELOPMENT; IN VIVO STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PROTEIN TRANSPORT;

EID: 33846232336     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2006.09.023     Document Type: Article

References (40)

1. Agarwal P., Wylie J.N., Galceran J., Arkhitko O., Li C., Deng C., Grosschedl R., and Bruneau B.G. Tbx5 is essential for forelimb bud initiation following patterning of the limb field in the mouse embryo. Development 130 (2003) 623-633
2. Basson C.T., Huang T., Lin R.C., Bachinsky D.R., Weremowicz S., Vaglio A., Bruzzone R., Quadrelli R., Lerone M., Romeo G., Silengo M., Pereira A., Krieger J., Mesquita S.F., Kamisago M., Morton C.C., Pierpont M.E., Muller C.W., Seidman J.G., and Seidman C.E. Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 2919-2924
3. Begemann G., and Ingham P.W. Developmental regulation of Tbx5 in zebrafish embryogenesis. Mech. Dev. 90 (2000) 299-304
4. Brassington A.E., Sung S.S., Toydemir R.M., Le T., Roeder A.D., Rutherford A.E., Whitby F.G., Jorde L.B., and Bamshad M.J. Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype. Am. J. Hum. (2003) 73
5. Bruneau B.G., Logan M., Davis N., Levi T., Tabin C.J., Seidman J.G., and Seidman C.E. Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome. Dev. Biol. 211 (1999) 100-108
6. Bruneau B.G., Nemer G., Schmitt J.P., Charron F., Robitaille L., Caron S., Conner D.A., Gessler M., Nemer M., Seidman C.E., and Seidman J.G. A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease. Cell 106 (2001) 709-721
7. Camarata T., Bimber B., Kulisz A., Yeung J., Chew T.L., and Simon H.G. LMP4 regulates Tbx5 protein sub-cellular localization and activity. J. Cell Biol. 174 (2001) 339-348
8. De la Cruz M.V., Gimenez-Ribotta M., Saravalli O., and Cayre R. 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. Am. J. Anat. 166 (1983) 63-72
9. Dettman R.W., Denetclaw Jr. W., Ordahl C.P., and Bristow J. Common epicardial origin of coronary vascular smooth muscle, perivascular fibroblasts, and intermyocardial fibroblasts in the avian heart. Dev. Biol. 193 (1998) 169-181
10. Gittenberger-de Groot A.C., Vrancken Peeters M.P., Mentink M.M., Gourdie R.G., and Poelmann R.E. Epicardium-derived cells contribute a novel population to the myocardial wall and the atrioventricular cushions. Circ. Res. 82 (1998) 1043-1052
11. Gittenberger-de Groot A.C., Vrancken Peeters M.P., Bergwerff M., Mentink M.M., and Poelmann R.E. Epicardial outgrowth inhibition leads to compensatory mesothelial outflow tract collar and abnormal cardiac septation and coronary formation. Circ. Res. 87 (2000) 969-971
12. Guy P.M., Kenny D.A., and Gill G.N. The PDZ domain of the LIM protein enigma binds to beta-tropomyosin. Mol. Biol. Cell 10 (1999) 1973-1984
13. Hamburger V., and Hamilton H.L. A series of normal stages in the development of the chick embryo. J. Morphol. 88 (1951) 49-92
14. Hatcher C.J., and McDermott D.A. Using the TBX5 transcription factor to grow and sculpt the heart. Am. J. Med. Genet. A 140 (2006) 1414-1418
15. Hatcher C.J., Kim M.S., Mah C.S., Goldstein M.M., Wong B., Mikawa T., and Basson C.T. TBX5 transcription factor regulates cell proliferation during cardiogenesis. Dev. Biol. 230 (2001) 177-188
16. Hatcher C.J., Diman N.Y., Kim M.S., Pennisi D., Song Y., Goldstein M.M., Mikawa T., and Basson C.T. A role for Tbx5 in proepicardial cell migration during cardiogenesis. Physiol. Genomics 18 (2004) 129-140
17. Kadrmas J.L., and Beckerle M.C. The LIM domain: from the cytoskeleton to the nucleus. Nat. Rev., Mol. Cell Biol. 5 (2004) 920-931
18. Kang J.O., and Sucov H.M. Convergent proliferative response and divergent morphogenic pathways induced by epicardial and endocardial signaling in fetal heart development. Mech. Dev. 122 (2005) 57-65
19. Khan P., Linkhart B., and Simon H.G. Different regulation of T-box genes Tbx4 and Tbx5 during limb development and limb regeneration. Dev. Biol. 250 (2002) 383-392
20. Krause A., Zacharias W., Camarata T., Linkhart B., Law E., Lischke A., Miljan E., and Simon H.G. Tbx5 and Tbx4 transcription factors interact with a new chicken PDZ-LIM protein in limb and heart development. Dev. Biol. 273 (2004) 106-120
21. Li Q.Y., Newbury-Ecob R.A., Terrett J.A., Wilson D.I., Curtis A.R.J., Yi C.H., Gebuhr T., Bullen P.J., Robson S.C., Strachan T., Bonnet D., Lyonnet S., Young I.D., Raeburn J.A., Buckler A.J., Law D.J., and Brook J.D. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. Nat. Genet. 15 (1997) 21-29
22. Liberatore C.M., Searcy-Schrick R.D., and Yutzey K.E. Ventricular expression of tbx5 inhibits normal heart chamber development. Dev. Biol. 223 (2000) 169-180
23. Lu J., Landerholm T.E., Wei J.S., Dong X.R., Wu S.P., Liu X., Nagata K., Inagaki M., and Majesky M.W. Coronary smooth muscle differentiation from proepicardial cells requires rhoA-mediated actin reorganization and p160 rho-kinase activity. Dev. Biol. 240 (2001) 404-418
24. Männer J. The development of pericardial villi in the chick embryo. Anat. Embryol. 186 (1992) 379-385
25. Manner J., Perez-Pomares J.M., Macias D., and Munoz-Chapuli R. The origin, formation and developmental significance of the epicardium: a review. Cells Tissues Organs 169 (2001) 89-103
26. Markwald R., Eisenberg C., Eisenberg L., Trusk T., and Sugi Y. Epithelial-mesenchymal transformations in early avian heart development. Acta Anat. (Basel) 156 (1996) 173-186
27. Merki E., Zamora M., Raya A., Kawakami Y., Wang J., Zhang X., Burch J., Kubalak S.W., Kaliman P., Belmonte J.C., Chien K.R., and Ruiz-Lozano P. Epicardial retinoid × receptor alpha is required for myocardial growth and coronary artery formation. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 18455-18460
28. Mori A.D., and Bruneau B.G. TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed. Curr. Opin. Cardiol. 19 (2004) 211-215
29. Mu H., Ohashi R., Lin P., Yao Q., and Chen C. Cellular and molecular mechanisms of coronary vessel development. Vasc. Med. 10 (2005) 37-44
30. Perez-Pomares J.M., Macias D., Garcia-Garrido L., and Munoz-Chapuli R. The origin of the subepicardial mesenchyme in the avian embryo: an immunohistochemical and quail-chick chimera study. Dev. Biol. 200 (1998) 57-68
31. Perez-Pomares J.M., Carmona R., Gonzalez-Iriarte M., Atencia G., Wessels A., and Munoz-Chapuli R. Origin of coronary endothelial cells from epicardial mesothelium in avian embryos. Int. J. Dev. Biol. 46 (2002) 1005-1013
32. Perez-Pomares J.M., Phelps A., Sedmerova M., and Wessels A. Epicardial-like cells on the distal arterial end of the cardiac outflow tract do not derive from the proepicardium but are derivatives of the cephalic pericardium. Dev. Dyn. 227 (2003) 56-68
33. Stuckmann I., Evans S., and Lassar A.B. Erythropoietin and retinoic acid, secreted from the epicardium, are required for cardiac myocyte proliferation. Dev. Biol. 255 (2003) 334-349
34. Takeuchi J.K., Ohgi M., Koshiba-Takeuchi K., Shiratori H., Sakaki I., Ogura K., Saijoh Y., and Ogura T. Tbx5 specifies the left/right ventricles and ventricular septum position during cardiogenesis. Development 130 (2003) 5953-5964
35. Vallenius T., Luukko K., and Makela T.P. CLP-36 PDZ-LIM protein associates with nonmuscle alpha-actinin-1 and alpha-actinin-4. J. Biol. Chem. 275 (2000) 11100-11105
36. Vaughan C.J., and Basson C.T. Molecular determinants of atrial and ventricular septal defects and patent ductus arteriosus. Am. J. Med. Genet. 97 (2000) 304-309
37. Viragh S., and Challice C.E. The origin of the epicardium and the embryonic myocardial circulation in the mouse. Anat. Rec. 201 (1981) 157-168
38. Viragh S., Szabo E., and Challice C.E. Formation of the primitive myo- and endocardial tubes in the chicken embryo. J. Mol. Cell Cardiol. 21 (1989) 123-137
39. Vrancken Peeters M.P., Gittenberger-de Groot A.C., Mentink M.M., and Poelmann R.E. Smooth muscle cells and fibroblasts of the coronary arteries derive from epithelial-mesenchymal transformation of the epicardium. Anat. Embryol. (Berl) 199 (1999) 367-378
40. Zhou Q., Ruiz-Lozano P., Martone M.E., and Chen J. Cypher, a striated muscle-restricted PDZ and LIM domain-containing protein, binds to alpha-actinin-2 and protein kinase C. J. Biol. Chem. 274 (1999) 19807-19813