Literature DB >> 10656773

Subdivision of the cardiac Nkx2.5 expression domain into myogenic and nonmyogenic compartments.

M Raffin1, L M Leong, M S Rones, D Sparrow, T Mohun, M Mercola.   

Abstract

Nkx2.5 is expressed in the cardiogenic mesoderm of avian, mouse, and amphibian embryos. To understand how various cardiac fates within this domain are apportioned, we fate mapped the mesodermal XNkx2.5 domain of neural tube stage Xenopus embryos. The lateral portions of the XNkx2.5 expression domain in the neural tube stage embryo (stage 22) form the dorsal mesocardium and roof of the pericardial cavity while the intervening ventral region closes to form the myocardial tube. XNkx2.5 expression is maintained throughout the period of heart tube morphogenesis and differentiation of myocardial, mesocardial, and pericardial tissues. A series of microsurgical experiments showed that myocardial differentiation in the lateral portion of the field is suppressed during normal development by signals from the prospective myocardium and by tissues located more dorsally in the embryo, in particular the neural tube. These signals combine to block myogenesis downstream of XNkx2.5 and at or above the level of contractile protein gene expression. We propose that the entire XNkx2.5/heart field is transiently specified as cardiomyogenic. Suppression of this program redirects lateral cells to adopt dorsal mesocardial and dorsal pericardial fates and subdivides the field into distinct myogenic and nonmyogenic compartments. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10656773     DOI: 10.1006/dbio.1999.9579

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


  21 in total

1.  Inhibition of Wnt activity induces heart formation from posterior mesoderm.

Authors:  M J Marvin; G Di Rocco; A Gardiner; S M Bush; A B Lassar
Journal:  Genes Dev       Date:  2001-02-01       Impact factor: 11.361

2.  Dlx proteins position the neural plate border and determine adjacent cell fates.

Authors:  Juliana M Woda; Julie Pastagia; Mark Mercola; Kristin Bruk Artinger
Journal:  Development       Date:  2003-01       Impact factor: 6.868

3.  Left and right contributions to the Xenopus heart: implications for asymmetric morphogenesis.

Authors:  Joseph P Gormley; Nanette M Nascone-Yoder
Journal:  Dev Genes Evol       Date:  2003-05-23       Impact factor: 0.900

Review 4.  Ciona intestinalis as a model for cardiac development.

Authors:  Brad Davidson
Journal:  Semin Cell Dev Biol       Date:  2006-12-20       Impact factor: 7.727

5.  Vessel and blood specification override cardiac potential in anterior mesoderm.

Authors:  Jeffrey J Schoenebeck; Brian R Keegan; Deborah Yelon
Journal:  Dev Cell       Date:  2007-08       Impact factor: 12.270

6.  SHP-2 is required for the maintenance of cardiac progenitors.

Authors:  Yvette G Langdon; Sarah C Goetz; Anna E Berg; Jackie Thomas Swanik; Frank L Conlon
Journal:  Development       Date:  2007-10-10       Impact factor: 6.868

7.  Wnt signals from the neural tube block ectopic cardiogenesis.

Authors:  E Tzahor; A B Lassar
Journal:  Genes Dev       Date:  2001-02-01       Impact factor: 11.361

8.  Proteomic profiling of cardiac tissue by isolation of nuclei tagged in specific cell types (INTACT).

Authors:  Nirav M Amin; Todd M Greco; Lauren M Kuchenbrod; Maggie M Rigney; Mei-I Chung; John B Wallingford; Ileana M Cristea; Frank L Conlon
Journal:  Development       Date:  2014-02       Impact factor: 6.868

Review 9.  Xenopus as a model system for vertebrate heart development.

Authors:  Andrew S Warkman; Paul A Krieg
Journal:  Semin Cell Dev Biol       Date:  2006-11-24       Impact factor: 7.727

10.  sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling.

Authors:  Natalie Gibb; Danielle L Lavery; Stefan Hoppler
Journal:  Development       Date:  2013-04       Impact factor: 6.868

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