Literature DB >> 9576835

The bHLH factors, dHAND and eHAND, specify pulmonary and systemic cardiac ventricles independent of left-right sidedness.

T Thomas1, H Yamagishi, P A Overbeek, E N Olson, D Srivastava.   

Abstract

dHAND and eHAND are basic helix-loop-helix transcription factors that play critical roles in cardiac development. The HAND genes have a complementary left-right cardiac asymmetry of expression with dHAND predominantly on the right side and eHAND on the left side of the looped heart tube. Here we show that although eHAND is asymmetrically expressed along the anterior-posterior and dorsal-ventral embryonic axes, it is symmetrically expressed along the left-right axis at early stages of embryonic and cardiac development. After cardiac looping, dHAND and eHAND are expressed in the right (pulmonary) and left (systemic) ventricles, respectively. The left-right (LR) sidedness of dHAND and eHAND expression is demonstrated to be anatomically reversed in situs inversus (inv/inv) mouse embryos; however, dHAND expression persists in the pulmonary ventricle and eHAND in the systemic ventricle regardless of anatomic position, indicating chamber specificity of expression. Previously we showed that dHAND-null mice fail to form a right-sided pulmonary ventricle. Here mice homozygous for the dHAND and inv mutations are demonstrated to have only a right-sided ventricle which is morphologically a left (systemic) ventricle. These data suggest that the HAND genes are involved in development of segments of the heart tube which give rise to specific chambers of the heart during cardiogenesis, rather than controlling the direction of cardiac looping by interpreting the cascade of LR embryonic signals.

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Year:  1998        PMID: 9576835     DOI: 10.1006/dbio.1998.8849

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  44 in total

Review 1.  The basic helix-loop-helix transcription factor, dHAND, is required for vascular development.

Authors:  H Yamagishi; E N Olson; D Srivastava
Journal:  J Clin Invest       Date:  2000-02       Impact factor: 14.808

2.  Disruption of hyaluronan synthase-2 abrogates normal cardiac morphogenesis and hyaluronan-mediated transformation of epithelium to mesenchyme.

Authors:  T D Camenisch; A P Spicer; T Brehm-Gibson; J Biesterfeldt; M L Augustine; A Calabro; S Kubalak; S E Klewer; J A McDonald
Journal:  J Clin Invest       Date:  2000-08       Impact factor: 14.808

3.  Full intrauterine development is compatible with cardia bifida in humans.

Authors:  V Demarchi Aiello; J Xavier-Neto
Journal:  Pediatr Cardiol       Date:  2006 May-Jun       Impact factor: 1.655

Review 4.  Transcriptional pathways in second heart field development.

Authors:  Brian L Black
Journal:  Semin Cell Dev Biol       Date:  2007-01-17       Impact factor: 7.727

5.  The Drosophila Hand gene is required for remodeling of the developing adult heart and midgut during metamorphosis.

Authors:  Patrick C H Lo; Stéphane Zaffran; Sébastien Sénatore; Manfred Frasch
Journal:  Dev Biol       Date:  2007-08-17       Impact factor: 3.582

6.  Wnt5a and Wnt11 are essential for second heart field progenitor development.

Authors:  Ethan David Cohen; Mayumi F Miller; Zichao Wang; Randall T Moon; Edward E Morrisey
Journal:  Development       Date:  2012-06       Impact factor: 6.868

7.  Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.

Authors:  Elizabeth Goldmuntz; Prasuna Paluru; Joseph Glessner; Hakon Hakonarson; Jaclyn A Biegel; Peter S White; Xiaowu Gai; Tamim H Shaikh
Journal:  Congenit Heart Dis       Date:  2011-10-20       Impact factor: 2.007

8.  A positive GATA element and a negative vitamin D receptor-like element control atrial chamber-specific expression of a slow myosin heavy-chain gene during cardiac morphogenesis.

Authors:  G F Wang; W Nikovits; M Schleinitz; F E Stockdale
Journal:  Mol Cell Biol       Date:  1998-10       Impact factor: 4.272

9.  The Polycomb-group gene Rae28 sustains Nkx2.5/Csx expression and is essential for cardiac morphogenesis.

Authors:  Manabu Shirai; Tomoaki Osugi; Hideyuki Koga; Yoshikazu Kaji; Eiki Takimoto; Issei Komuro; Junichi Hara; Takeshi Miwa; Keiko Yamauchi-Takihara; Yoshihiro Takihara
Journal:  J Clin Invest       Date:  2002-07       Impact factor: 14.808

10.  Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart.

Authors:  Chen-Leng Cai; Xingqun Liang; Yunqing Shi; Po-Hsien Chu; Samuel L Pfaff; Ju Chen; Sylvia Evans
Journal:  Dev Cell       Date:  2003-12       Impact factor: 12.270

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