|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 118, Issue 3 865-875, Copyright © 1993 by Company of Biologists
JOURNAL ARTICLES |
M Logan and T Mohun
Laboratory of Developmental Biochemistry, National Institute for Medical Research, London, UK.
We have isolated a cDNA fragment encoding a portion of the myosin heavy chain alpha-isoform (XMHC alpha) in the amphibian, Xenopus laevis. The XMHC alpha transcript is highly enriched in adult heart RNA and is expressed exclusively in embryonic heart tissue. It therefore provides a tissue-specific marker for cardiac muscle differentiation during early embryogenesis. Using an RNAase protection assay, we can detect the onset of cardiac muscle differentiation in an anterior, ventral region of tailbud embryos, many hours before the appearance of a beating heart. Whole-mount in situ RNA hybridisation indicates that expression of the XMHC alpha gene is restricted to the developing heart primordium. XMHC alpha gene expression can also be induced in isolated animal pole explants of blastulae by treatment with the growth factor, activin A. Induction is dose-dependent, requiring high doses of the growth factor compared with that required for myotomal (skeletal) muscle differentiation. In contrast, no XMHC alpha transcripts are detected in explants incubated with basic FGF, despite the induction of myotomal muscle differentiation. Activin-induced explants show a similar temporal pattern of XMHC alpha gene expression to that found in normal embryogenesis. Furthermore, cells expressing this gene appear clustered in one or two foci within fused explant aggregates, which often show regular, spontaneous contractions after several days in culture. These results show that terminal differentiation of cardiac muscle can occur in growth factor-induced explants and may be distinguished from skeletal muscle differentiation by the dose and nature of the inducing factor.
This article has been cited by other articles:
![]() |
D. D. Brown, S. N. Martz, O. Binder, S. C. Goetz, B. M. J. Price, J. C. Smith, and F. L. Conlon Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis Development, February 1, 2005; 132(3): 553 - 563. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Dell'Era, R. Ronca, L. Coco, S. Nicoli, M. Metra, and M. Presta Fibroblast Growth Factor Receptor-1 Is Essential for In Vitro Cardiomyocyte Development Circ. Res., September 5, 2003; 93(5): 414 - 420. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. V. Latinkic, S. Kotecha, and T. J. Mohun Induction of cardiomyocytes by GATA4 in Xenopus ectodermal explants Development, August 15, 2003; 130(16): 3865 - 3876. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Nakamura, M. Sano, Z. Songyang, and M. D. Schneider A Wnt- and beta -catenin-dependent pathway for mammalian cardiac myogenesis PNAS, May 13, 2003; 100(10): 5834 - 5839. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. L. Waldo, D. H. Kumiski, K. T. Wallis, H. A. Stadt, Mary. R. Hutson, D. H. Platt, and M. L. Kirby Conotruncal myocardium arises from a secondary heart field Development, August 15, 2001; 128(16): 3179 - 3188. [Abstract] [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
Y Fu, W Yan, T. Mohun, and S. Evans Vertebrate tinman homologues XNkx2-3 and XNkx2-5 are required for heart formation in a functionally redundant manner Development, January 11, 1998; 125(22): 4439 - 4449. [Abstract] [PDF] |
||||
![]() |
D. Sparrow, W. Jen, S Kotecha, N Towers, C Kintner, and T. Mohun Thylacine 1 is expressed segmentally within the paraxial mesoderm of the Xenopus embryo and interacts with the Notch pathway Development, January 6, 1998; 125(11): 2041 - 2051. [Abstract] [PDF] |
||||
![]() |
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] |
||||
![]() |
C. A. Eisenberg and D. M. Bader Establishment of the Mesodermal Cell Line QCE-6 : A Model System for Cardiac Cell Differentiation Circ. Res., February 1, 1996; 78(2): 205 - 216. [Abstract] [Full Text] |
||||
![]() |
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] |
||||
![]() |
I Lyons, L M Parsons, L Hartley, R Li, J E Andrews, L Robb, and R P Harvey Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5. Genes & Dev., July 1, 1995; 9(13): 1654 - 1666. [Abstract] [PDF] |
||||
![]() |
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] |
||||
![]() |
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] |
||||