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Desmosomal cadherins in zebrafish epiboly and gastrulation

BACKGROUND: The desmosomal cadherins (DCs), desmocollin (Dsc) and desmoglein (Dsg), are the adhesion molecules of desmosomes, intercellular adhesive junctions of epithelia and cardiac muscle. Both the DCs and desmosomes have demonstrably essential roles in mammalian development. In order to initiate...

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Autores principales: Goonesinghe, Alexander, Luan, Xing-Ming, Hurlstone, Adam, Garrod, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268089/
https://www.ncbi.nlm.nih.gov/pubmed/22235774
http://dx.doi.org/10.1186/1471-213X-12-1
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author Goonesinghe, Alexander
Luan, Xing-Ming
Hurlstone, Adam
Garrod, David
author_facet Goonesinghe, Alexander
Luan, Xing-Ming
Hurlstone, Adam
Garrod, David
author_sort Goonesinghe, Alexander
collection PubMed
description BACKGROUND: The desmosomal cadherins (DCs), desmocollin (Dsc) and desmoglein (Dsg), are the adhesion molecules of desmosomes, intercellular adhesive junctions of epithelia and cardiac muscle. Both the DCs and desmosomes have demonstrably essential roles in mammalian development. In order to initiate their study in a more tractable developmental system we have characterised zebrafish DCs and examined their roles in early zebrafish development. RESULTS: We find that zebrafish possess one Dsc, the orthologue of mammalian Dsc1, which we designate zfDsc. Unlike mammalian Dscs, zfDsc exists only as the "a" form since it lacks the alternatively-spliced mini-exon that shortens the cytoplasmic domain to produce the "b" form. Zebrafish possess two Dsgs, designated zfDsgα and zfDsgβ, orthologues of mammalian Dsg2. They show 43.8% amino acid identity and the α form has a 43 amino acid glycine-rich sequence of unknown function in its extracellular domain. Both zfDsc and zfDsgα were present as maternal and zygotic transcripts whereas zfDsgβ was first expressed from 8 hours post-fertilisation (hpf). All three transcripts were present throughout subsequent stages of development. Morpholino knockdown of both zfDsc and zfDsgα expression produced similar defects in epiboly, axis elongation and somite formation, associated with abnormal desmosomes or reduced desmosome numbers. CONCLUSIONS: These results demonstrate an important role for DCs and desmosomes in the early morphogenesis of the zebrafish embryo, provide a basis for more detailed analysis of their role and raise interesting questions relating to the evolution and functional significance of DC isoforms.
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spelling pubmed-32680892012-01-30 Desmosomal cadherins in zebrafish epiboly and gastrulation Goonesinghe, Alexander Luan, Xing-Ming Hurlstone, Adam Garrod, David BMC Dev Biol Research Article BACKGROUND: The desmosomal cadherins (DCs), desmocollin (Dsc) and desmoglein (Dsg), are the adhesion molecules of desmosomes, intercellular adhesive junctions of epithelia and cardiac muscle. Both the DCs and desmosomes have demonstrably essential roles in mammalian development. In order to initiate their study in a more tractable developmental system we have characterised zebrafish DCs and examined their roles in early zebrafish development. RESULTS: We find that zebrafish possess one Dsc, the orthologue of mammalian Dsc1, which we designate zfDsc. Unlike mammalian Dscs, zfDsc exists only as the "a" form since it lacks the alternatively-spliced mini-exon that shortens the cytoplasmic domain to produce the "b" form. Zebrafish possess two Dsgs, designated zfDsgα and zfDsgβ, orthologues of mammalian Dsg2. They show 43.8% amino acid identity and the α form has a 43 amino acid glycine-rich sequence of unknown function in its extracellular domain. Both zfDsc and zfDsgα were present as maternal and zygotic transcripts whereas zfDsgβ was first expressed from 8 hours post-fertilisation (hpf). All three transcripts were present throughout subsequent stages of development. Morpholino knockdown of both zfDsc and zfDsgα expression produced similar defects in epiboly, axis elongation and somite formation, associated with abnormal desmosomes or reduced desmosome numbers. CONCLUSIONS: These results demonstrate an important role for DCs and desmosomes in the early morphogenesis of the zebrafish embryo, provide a basis for more detailed analysis of their role and raise interesting questions relating to the evolution and functional significance of DC isoforms. BioMed Central 2012-01-11 /pmc/articles/PMC3268089/ /pubmed/22235774 http://dx.doi.org/10.1186/1471-213X-12-1 Text en Copyright ©2012 Goonesinghe et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Goonesinghe, Alexander
Luan, Xing-Ming
Hurlstone, Adam
Garrod, David
Desmosomal cadherins in zebrafish epiboly and gastrulation
title Desmosomal cadherins in zebrafish epiboly and gastrulation
title_full Desmosomal cadherins in zebrafish epiboly and gastrulation
title_fullStr Desmosomal cadherins in zebrafish epiboly and gastrulation
title_full_unstemmed Desmosomal cadherins in zebrafish epiboly and gastrulation
title_short Desmosomal cadherins in zebrafish epiboly and gastrulation
title_sort desmosomal cadherins in zebrafish epiboly and gastrulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268089/
https://www.ncbi.nlm.nih.gov/pubmed/22235774
http://dx.doi.org/10.1186/1471-213X-12-1
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