Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
Development
2005 Feb 01;1323:553-63. doi: 10.1242/dev.01596.
Show Gene links
Show Anatomy links
Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis.
Brown DD
,
Martz SN
,
Binder O
,
Goetz SC
,
Price BM
,
Smith JC
,
Conlon FL
.
???displayArticle.abstract???
Members of the T-box family of proteins play a fundamental role in patterning the developing vertebrate heart; however, the precise cellular requirements for any one family member and the mechanism by which individual T-box genes function remains largely unknown. In this study, we have investigated the cellular and molecular relationship between two T-box genes, Tbx5 and Tbx20. We demonstrate that blocking Tbx5 or Tbx20 produces phenotypes that display a high degree of similarity, as judged by overall gross morphology, molecular marker analysis and cardiac physiology, implying that the two genes are required for and have non-redundant functions in early heart development. In addition, we demonstrate that although co-expressed, Tbx5 and Tbx20 are not dependent on the expression of one another, but rather have a synergistic role during early heart development. Consistent with this proposal, we show that TBX5 and TBX20 can physically interact and map the interaction domains, and we show a cellular interaction for the two proteins in cardiac development, thus providing the first evidence for direct interaction between members of the T-box gene family.
Fig. 5. TBX5 and TBX20 morphants display dramatic morphological defects. Whole-mount in situ hybridization of cleared stage 36 embryos. (A-C) ANF whole-mount in situ hybridization. (D-F) XTnIc whole-mount in situ hybridization. (A,D) ControlMO. (B,E) TBX5MO and (C,F) TBX20MO.
Fig. 9. Tbx5 and Tbx20 synergistically act to regulate cardiac gene expression. (A-L) Embryos injected with the indicated morpholinos at the one-cell stage. (A-D) Nkx2-5 whole-mount in situ hybridization. (E-H) XANF whole-mount in situ hybridization. (I-L) XTnIc whole-mount in situ hybridization. (A,E,I) ControlMO, (B,F,J) TBX5MO injected at suboptimal dose, (C,G,K) TBX20MO injected at suboptimal dose, (D,H,L) TBX5MO and TBX20MO injected in combination at suboptimal doses. All embryo were cleared to reveal heart expression. (M) Statistics for embryos injected with suboptimal doses of TBX5MO and TBX20MO in combination with each other or with ControlMO. Hearts were judged as having defects if they displayed a pericardial edema, an unlooped heart tube or reduction in cardiac mass.
Fig. 3. TBX5 and TBX20 morphants fail to undergo looping and chamber formation and display reduced cardiac cell numbers. Cryosections of TBX5 and TBX20 morphant hearts taken at the anterior (outflow), middle (ventricular) and posterior (atrial) regions. (A-D) ControlMO, (E-H) TBX5MO and (I-L) TBX20MO. Sections stained for tropomyosin (red), DAPI (blue) and cardiac actin (green). (D,H,L) Same sections as B, F and J stained with cardiac actin. In the looped control heart, the middle ventricular section also contains the atrium. (M) Mean number of cells per heart obtained by cell counts of hearttissue in serial sections derived from a minimum of three embryos.
Fig. 4. Cardiac specification is unaltered in TBX5 and TBX20 morphants. Whole-mount in situ with Nkx2.5 on stage matched (A,D,G,J) ControlMO-, (B,E,H,K) TBX5MO- or (C,F,I,L) TBX20MO-derived embryos.
Fig. 7. Tbx5 and Tbx20 are not required for the expression of each other. Embryos injected at the one-cell stage with ControlMO, TBX5MO or TBX20MO. (A,C) Whole-mount in situ hybridization showing Tbx5 expression. (B,D) Whole-mount in situ hybridization showing Tbx20 expression.
Fig. S2. Tbx5 is expressed in the common cardinal and anterior hepatic veins. (A,B) Whole-mount in situ hybridization of Xenopus embryos at stage 36 (A) and 42 (B). Parasaggital section show expression in the myocardium (m), endocardium (e) and pericardium (p). (C,D) Oblique sections through a stage 36 embryo showing expression in the common cardinal (cc) and anterior hepatic veins (h).
Fig. S3. Tbx5 and Tbx20 morpholinos block the formation of a functional heart as assayed by benzidine staining of erythrocytes in stage 42 tadpoles. (A) Uninjected control, (B) TBX5MO injected at optimal dose, (C) TBX20MO injected at optimal dose, (D) TBX5MO and TBX20MO injected together at suboptimal doses. There is blood staining in the heart region (h) of control embryos but not in morphant embryos.
Fig. 2. Tbx5 and Tbx20 are required for proper cardiogenesis.
(A-F) Morpholino injected tadpoles at the indicated stages. Control morphant embryos (A,D), TBX5 morphant embryos (B,E) and TBX20 morphant embryos (C,F). Arrows indicate the heart region, arrowheads indicate the eye. (G) Chart displaying the percentage of morphants surviving and displaying cardiac abnormalities, as scored by the presence of an unlooped heart tube, a reduction in cardiac mass and the presence of a pericardial edema.
Baldini,
DiGeorge syndrome: an update.
2004, Pubmed
Baldini,
DiGeorge syndrome: an update.
2004,
Pubmed
Basson,
Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.
1997,
Pubmed
Basson,
Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations.
1999,
Pubmed
Benson,
New understandings in the genetics of congenital heart disease.
1996,
Pubmed
Brown,
Developmental expression of the Xenopus laevis Tbx20 orthologue.
2003,
Pubmed
,
Xenbase
Bruneau,
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease.
2001,
Pubmed
Carson,
Tbx12 regulates eye development in Xenopus embryos.
2004,
Pubmed
,
Xenbase
Chapman,
Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.
1996,
Pubmed
Chieffo,
Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.
1997,
Pubmed
,
Xenbase
Collavoli,
TBX5 nuclear localization is mediated by dual cooperative intramolecular signals.
2003,
Pubmed
Cripps,
Control of cardiac development by an evolutionarily conserved transcriptional network.
2002,
Pubmed
Drysdale,
Cardiac troponin I is a heart-specific marker in the Xenopus embryo: expression during abnormal heart morphogenesis.
1994,
Pubmed
,
Xenbase
Elliott,
Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
2003,
Pubmed
,
Xenbase
Fan,
Functional analysis of TBX5 missense mutations associated with Holt-Oram syndrome.
2003,
Pubmed
Garrity,
The heartstrings mutation in zebrafish causes heart/fin Tbx5 deficiency syndrome.
2002,
Pubmed
Goldmuntz,
NKX2.5 mutations in patients with tetralogy of fallot.
2001,
Pubmed
,
Xenbase
Harland,
In situ hybridization: an improved whole-mount method for Xenopus embryos.
1991,
Pubmed
,
Xenbase
Harvey,
Patterning the vertebrate heart.
2002,
Pubmed
Heasman,
Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach.
2000,
Pubmed
,
Xenbase
Hiroi,
Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation.
2001,
Pubmed
,
Xenbase
Hoffman,
Incidence of congenital heart disease: I. Postnatal incidence.
1995,
Pubmed
Hoffman,
Incidence of congenital heart disease: II. Prenatal incidence.
1995,
Pubmed
Horb,
A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation.
1997,
Pubmed
,
Xenbase
Horb,
Tbx5 is essential for heart development.
1999,
Pubmed
,
Xenbase
Jerome,
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.
2001,
Pubmed
Kolker,
Confocal imaging of early heart development in Xenopus laevis.
2000,
Pubmed
,
Xenbase
Koshiba-Takeuchi,
Tbx5 and the retinotectum projection.
2000,
Pubmed
Laverriere,
GATA-4/5/6, a subfamily of three transcription factors transcribed in developing heart and gut.
1994,
Pubmed
Leconte,
Pax6 interacts with cVax and Tbx5 to establish the dorsoventral boundary of the developing eye.
2004,
Pubmed
Li,
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
1997,
Pubmed
Lindsay,
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
2001,
Pubmed
Logan,
Induction of cardiac muscle differentiation in isolated animal pole explants of Xenopus laevis embryos.
1993,
Pubmed
,
Xenbase
Marcellini,
Evolution of Brachyury proteins: identification of a novel regulatory domain conserved within Bilateria.
2003,
Pubmed
,
Xenbase
Merscher,
TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
2001,
Pubmed
Mohun,
The morphology of heart development in Xenopus laevis.
2000,
Pubmed
,
Xenbase
Moskowitz,
The T-Box transcription factor Tbx5 is required for the patterning and maturation of the murine cardiac conduction system.
2004,
Pubmed
Newbury-Ecob,
Holt-Oram syndrome: a clinical genetic study.
1996,
Pubmed
Packham,
T-box genes in human disorders.
2003,
Pubmed
Payne,
Toward a molecular understanding of congenital heart disease.
1995,
Pubmed
Plageman,
Differential expression and function of Tbx5 and Tbx20 in cardiac development.
2004,
Pubmed
Prall,
Developmental paradigms in heart disease: insights from tinman.
2002,
Pubmed
,
Xenbase
Ryan,
T-box genes and cardiac development.
2003,
Pubmed
Serbedzija,
Regulation in the heart field of zebrafish.
1998,
Pubmed
,
Xenbase
Showell,
T-box genes in early embryogenesis.
2004,
Pubmed
,
Xenbase
Small,
Expression of atrial natriuretic factor (ANF) during Xenopus cardiac development.
2000,
Pubmed
,
Xenbase
Stennard,
Cardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heart.
2003,
Pubmed
,
Xenbase
Szeto,
HrT is required for cardiovascular development in zebrafish.
2002,
Pubmed
Tonissen,
XNkx-2.5, a Xenopus gene related to Nkx-2.5 and tinman: evidence for a conserved role in cardiac development.
1994,
Pubmed
,
Xenbase
Wilson,
Induction of epidermis and inhibition of neural fate by Bmp-4.
1995,
Pubmed
,
Xenbase
Yagi,
Role of TBX1 in human del22q11.2 syndrome.
2003,
Pubmed
Zaffran,
Early signals in cardiac development.
2002,
Pubmed
Zaragoza,
Identification of the TBX5 transactivating domain and the nuclear localization signal.
2004,
Pubmed