spacer gif spacer gif spacer gif spacer gif ARCHIVE ANNOUNCEMENT! spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sater, A. K.
Right arrow Articles by Jacobson, A. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sater, A. K.
Right arrow Articles by Jacobson, A. G.

Development, Vol 105, Issue 4 821-830, Copyright © 1989 by Company of Biologists


JOURNAL ARTICLES

The specification of heart mesoderm occurs during gastrulation in Xenopus laevis

AK Sater and AG Jacobson
Department of Zoology, University of Texas, Austin 78712.

The establishment of heart mesoderm during Xenopus development has been examined using an assay for heart differentiation in explants and explant combinations in culture. Previous studies using urodele embryos have shown that the heart mesoderm is induced by the prospective pharyngeal endoderm during neurula and postneurula stages. In this study, we find that the specification of heart mesoderm must begin well before the end of gastrulation in Xenopus embryos. Explants of prospective heart mesoderm isolated from mid- or late neurula stages were capable of heart formation in nearly 100% of cases, indicating that the specification of heart mesoderm is complete by midneurula stages. Moreover, inclusion of pharyngeal endoderm had no statistically significant effect upon either the frequency of heart formation or the timing of the initiation of heartbeat in explants of prospective heart mesoderm isolated after the end of gastrulation. When the superficial pharyngeal endoderm was removed at the beginning of gastrulation, experimental embryos formed hearts, as did explants of prospective heart mesoderm from such embryos. These results indicate that the inductive interactions responsible for the establishment of heart mesoderm occur prior to the end of gastrulation and do not require the participation of the superficial pharyngeal endoderm.


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
K. Harada, A. Ogai, T. Takahashi, M. Kitakaze, H. Matsubara, and H. Oh
Crossveinless-2 Controls Bone Morphogenetic Protein Signaling during Early Cardiomyocyte Differentiation in P19 Cells
J. Biol. Chem., September 26, 2008; 283(39): 26705 - 26713.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
Y. G. Langdon, S. C. Goetz, A. E. Berg, J. T. Swanik, and F. L. Conlon
SHP-2 is required for the maintenance of cardiac progenitors
Development, November 15, 2007; 134(22): 4119 - 4130.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
A. Litsiou, S. Hanson, and A. Streit
A balance of FGF, BMP and WNT signalling positions the future placode territory in the head
Development, September 15, 2005; 132(18): 4051 - 4062.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
K.-H. Lee, S. Evans, T. Y. Ruan, and A. B. Lassar
SMAD-mediated modulation of YY1 activity regulates the BMP response and cardiac-specific expression of a GATA4/5/6-dependent chick Nkx2.5 enhancer
Development, October 1, 2004; 131(19): 4709 - 4723.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
V. A. Schneider and M. Mercola
Wnt antagonism initiates cardiogenesis in Xenopus laevis
Genes & Dev., February 1, 2001; 15(3): 304 - 315.
[Abstract] [Full Text]


Home page
DevelopmentHome page
M. Rones, K. McLaughlin, M Raffin, and M Mercola
Serrate and Notch specify cell fates in the heart field by suppressing cardiomyogenesis
Development, January 9, 2000; 127(17): 3865 - 3876.
[Abstract] [PDF]


Home page
DevelopmentHome page
J. Reecy, X Li, M Yamada, F. DeMayo, C. Newman, R. Harvey, and R. Schwartz
Identification of upstream regulatory regions in the heart-expressed homeobox gene Nkx2-5
Development, January 2, 1999; 126(4): 839 - 849.
[Abstract] [PDF]


Home page
DevelopmentHome page
G. Serbedzija, J. Chen, and M. Fishman
Regulation in the heart field of zebrafish
Development, January 3, 1998; 125(6): 1095 - 1101.
[Abstract] [PDF]


Home page
Genes Dev.Home page
T M Schultheiss, J B Burch, and A B Lassar
A role for bone morphogenetic proteins in the induction of cardiac myogenesis.
Genes & Dev., February 15, 1997; 11(4): 451 - 462.
[Abstract] [PDF]


Home page
DevelopmentHome page
K Sampath, A. Cheng, A Frisch, and C. Wright
Functional differences among Xenopus nodal-related genes in left-right axis determination
Development, January 9, 1997; 124(17): 3293 - 3302.
[Abstract] [PDF]


Home page
DevelopmentHome page
P. Tam, M Parameswaran, S. Kinder, and R. Weinberger
The allocation of epiblast cells to the embryonic heart and other mesodermal lineages: the role of ingression and tissue movement during gastrulation
Development, January 5, 1997; 124(9): 1631 - 1642.
[Abstract] [PDF]


Home page
DevelopmentHome page
O. Cleaver, K. Patterson, and P. Krieg
Overexpression of the tinman-related genes XNkx-2.5 and XNkx-2.3 in Xenopus embryos results in myocardial hyperplasia
Development, January 11, 1996; 122(11): 3549 - 3556.
[Abstract] [PDF]


Home page
DevelopmentHome page
T. Schultheiss, S Xydas, and A. Lassar
Induction of avian cardiac myogenesis by anterior endoderm
Development, January 12, 1995; 121(12): 4203 - 4214.
[Abstract] [PDF]


Home page
DevelopmentHome page
S. Evans, W Yan, M. Murillo, J Ponce, and N Papalopulu
tinman, a Drosophila homeobox gene required for heart and visceral mesoderm specification, may be represented by a family of genes in vertebrates: XNkx-2.3, a second vertebrate homologue of tinman
Development, January 11, 1995; 121(11): 3889 - 3899.
[Abstract] [PDF]


Home page
DevelopmentHome page
M Gannon and D Bader
Initiation of cardiac differentiation occurs in the absence of anterior endoderm
Development, January 8, 1995; 121(8): 2439 - 2450.
[Abstract] [PDF]


Home page
DevelopmentHome page
N Nascone and M Mercola
An inductive role for the endoderm in Xenopus cardiogenesis
Development, January 2, 1995; 121(2): 515 - 523.
[Abstract] [PDF]


Home page
Genes Dev.Home page
A E Chambers, M Logan, S Kotecha, N Towers, D Sparrow, and T J Mohun
The RSRF/MEF2 protein SL1 regulates cardiac muscle-specific transcription of a myosin light-chain gene in Xenopus embryos.
Genes & Dev., June 1, 1994; 8(11): 1324 - 1334.
[Abstract] [PDF]


Home page
DevelopmentHome page
M Logan and T Mohun
Induction of cardiac muscle differentiation in isolated animal pole explants of Xenopus laevis embryos
Development, January 7, 1993; 118(3): 865 - 875.
[Abstract] [PDF]


Home page
Genes Dev.Home page
H L Sive, B W Draper, R M Harland, and H Weintraub
Identification of a retinoic acid-sensitive period during primary axis formation in Xenopus laevis.
Genes & Dev., June 1, 1990; 4(6): 932 - 942.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
L. M. Pabon-Pena, R. L. Goodwin, L. J. Cise, and D. Bader
Analysis of CMF1 Reveals a Bone Morphogenetic Protein-independent Component of the Cardiomyogenic Pathway
J. Biol. Chem., July 7, 2000; 275(28): 21453 - 21459.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1989