|
|
| Research article summary (published 29 Sep 2009): |
The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment.
Full Abstract
The skeletal muscle basement membrane fulfils several crucial functions during development and in the mature myotome and defects in its composition underlie certain forms of muscular dystrophy. A major component of this extracellular structure is the laminin polymer, which assembles into a resilient meshwork that protects the sarcolemma during contraction. Here we describe a zebrafish mutant, softy, which displays severe embryonic muscle degeneration as a result of initial basement membrane failure. The softy phenotype is caused by a mutation in the lamb2 gene, identifying laminin beta2 as an essential component of this basement membrane. Uniquely, softy homozygotes are able to recover and survive to adulthood despite the loss of myofibre adhesion. We identify the formation of ectopic, stable basement membrane attachments as a novel means by which detached fibres are able to maintain viability. This demonstration of a muscular dystrophy model possessing innate fibre viability following muscle detachment suggests basement membrane augmentation as a therapeutic strategy to inhibit myofibre loss.
Author information
Author/s: Jacoby, Arie S (AS); Busch-Nentwich, Elisabeth (E); Bryson-Richardson, Robert J (RJ); Hall, Thomas E (TE); Berger, Joachim (J); Berger, Silke (S); Sonntag, Carmen (C); Sachs, Caroline (C); Geisler, Robert (R); Stemple, Derek L (DL); Currie, Peter D (PD);
Affiliation: The Victor Chang Cardiac Research Institute, Darlinghurst, NSW 2010, Australia.
Grants: WT 077037/Z/05/Z (Agency:Wellcome Trust) ; WT 077047/Z/05/Z (Agency:Wellcome Trust)
Journal and publication information
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal: Development (Cambridge, England) (Development), published in England. (Language: eng)
Reference: 2009-Oct; vol 136 (issue 19) : pp 3367-76
Dates: Created 2009/09/08; Completed 2009/10/14;
PMID: 19736328, status: MEDLINE (last retrieval date: 10/14/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
External Links for this article
(including full text providers, if available):
Click Electronic Full-text Provider Links to see options for finding the electronic full text links to this article. Note there may be a subscription or fee required for access to the full text. See our FAQ for information on finding FREE full text articles.
This article may also be located in paper journal collections available in many libraries. Use the Journal and Publication Information above to find the full article.
MeSH headings (categories)
This article was linked to the MESH Headings shown below.
Related articles
These are the highest related articles currently in the database:
- Transient axonal glycoprotein-1 (TAG-1) and laminin-alpha1 regulate dynamic growth cone behaviors and initial axon direction in vivo.
18 Feb 2008 - Regulation and function of foxe3 during early zebrafish development.
28 Feb 2008 - Ectopic expression and knockdown of a zebrafish sox21 reveal its role as a transcriptional repressor in early development.
30 Jan 2004 - Positional cloning of a temperature-sensitive mutant emmental reveals a role for sly1 during cell proliferation in zebrafish fin regeneration.
13 Jun 2003 - Gene duplication and functional divergence of the zebrafish insulin-like growth factor 1 receptors.
14 May 2006 - A direct role for Sox10 in specification of neural crest-derived sensory neurons.
23 Oct 2006 - Essential and overlapping roles for laminin alpha chains in notochord and blood vessel formation.
30 Dec 2005 - Tbx2b is essential for neuronal differentiation along the dorsal/ventral axis of the zebrafish retina.
6 Mar 2005 - Misty somites, a maternal effect gene identified by transposon-mediated insertional mutagenesis in zebrafish that is essential for the somite boundary maintenance.
11 Feb 2008 - laminin alpha 1 gene is essential for normal lens development in zebrafish.
5 Mar 2006
Related Article Map
Legend:
- FREE Full text Article.
- Abstract only.
- Title only. More help.
See a large map of 100+ related articles.