|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
First published online 1 September 2004
doi: 10.1242/dev.01374
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 MRC Human Genetics Unit, Western General Hospital, Crewe Road, Edinburgh EH4
2XU, UK
2 The Victor Chang Cardiac Research Institute, 384 Victoria Street, Darlinghurst
2010, NSW, Australia
* Author for correspondence (e-mail: p.currie{at}victorchang.unsw.edu.au)
Accepted 15 July 2004
Somites give rise to a number of different embryonic cell types, including the precursors of skeletal muscle populations. The lateral aspect of amniote and fish somites have been shown to give rise specifically to hypaxial muscle, including the appendicular muscle that populates fins and limbs. We have investigated the morphogenetic basis for formation of specific hypaxial muscles within the zebrafish embryo and larvae. Transplantation experiments have revealed a developmentally precocious commitment of cells derived from pectoral fin level somites to forming hypaxial and specifically appendicular muscle. The fate of transplanted somites cannot be over-ridden by local inductive signals, suggesting that somitic tissue may be fixed at an early point in their developmental history to produce appendicular muscle. We further show that this restriction in competence is mirrored at the molecular level, with the exclusive expression of the receptor tyrosine kinase met within somitic regions fated to give rise to appendicular muscle. Loss-of-function experiments reveal that Met and its ligand, hepatocyte growth factor, are required for the correct morphogenesis of the hypaxial muscles in which met is expressed. Furthermore, we demonstrate a requirement for Met signaling in the process of proneuromast deposition from the posterior lateral line primordia.
Key words: Hypaxial muscle, Met, Zebrafish
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati
Twitter What's this?
This article has been cited by other articles:
![]() |
D. Hava, U. Forster, M. Matsuda, S. Cui, B. A. Link, J. Eichhorst, B. Wiesner, A. Chitnis, and S. Abdelilah-Seyfried Apical membrane maturation and cellular rosette formation during morphogenesis of the zebrafish lateral line J. Cell Sci., March 1, 2009; 122(5): 687 - 695. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Hinits, D. P. S. Osborn, and S. M. Hughes Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations Development, February 1, 2009; 136(3): 403 - 414. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Elworthy, M. Hargrave, R. Knight, K. Mebus, and P. W. Ingham Expression of multiple slow myosin heavy chain genes reveals a diversity of zebrafish slow twitch muscle fibres with differing requirements for Hedgehog and Prdm1 activity Development, June 15, 2008; 135(12): 2115 - 2126. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. J. Carney, S. von der Hardt, C. Sonntag, A. Amsterdam, J. Topczewski, N. Hopkins, and M. Hammerschmidt Inactivation of serine protease Matriptase1a by its inhibitor Hai1 is required for epithelial integrity of the zebrafish epidermis Development, October 1, 2007; 134(19): 3461 - 3471. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Ghysen and C. Dambly-Chaudiere The lateral line microcosmos Genes & Dev., September 1, 2007; 21(17): 2118 - 2130. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Svetic, G. E. Hollway, S. Elworthy, T. R. Chipperfield, C. Davison, R. J. Adams, J. S. Eisen, P. W. Ingham, P. D. Currie, and R. N. Kelsh Sdf1a patterns zebrafish melanophores and links the somite and melanophore pattern defects in choker mutants Development, March 1, 2007; 134(5): 1011 - 1022. [Abstract] [Full Text] [PDF] |
||||