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Cloning, Annotation and Developmental Expression of the Chicken Intestinal MUC2 Gene

Intestinal mucin 2 (MUC2) encodes a heavily glycosylated, gel-forming mucin, which creates an important protective mucosal layer along the gastrointestinal tract in humans and other species. This first line of defense guards against attacks from microorganisms and is integral to the innate immune sy...

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Autores principales: Jiang, Zhengyu, Applegate, Todd J., Lossie, Amy C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549977/
https://www.ncbi.nlm.nih.gov/pubmed/23349743
http://dx.doi.org/10.1371/journal.pone.0053781
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author Jiang, Zhengyu
Applegate, Todd J.
Lossie, Amy C.
author_facet Jiang, Zhengyu
Applegate, Todd J.
Lossie, Amy C.
author_sort Jiang, Zhengyu
collection PubMed
description Intestinal mucin 2 (MUC2) encodes a heavily glycosylated, gel-forming mucin, which creates an important protective mucosal layer along the gastrointestinal tract in humans and other species. This first line of defense guards against attacks from microorganisms and is integral to the innate immune system. As a first step towards characterizing the innate immune response of MUC2 in different species, we report the cloning of a full-length, 11,359 bp chicken MUC2 cDNA, and describe the genomic organization and functional annotation of this complex, 74.5 kb locus. MUC2 contains 64 exons and demonstrates distinct spatiotemporal expression profiles throughout development in the gastrointestinal tract; expression increases with gestational age and from anterior to posterior along the gut. The chicken protein has a similar domain organization as the human orthologue, with a signal peptide and several von Willebrand domains in the N-terminus and the characteristic cystine knot at the C-terminus. The PTS domain of the chicken MUC2 protein spans ∼1600 amino acids and is interspersed with four CysD motifs. However, the PTS domain in the chicken diverges significantly from the human orthologue; although the chicken domain is shorter, the repetitive unit is 69 amino acids in length, which is three times longer than the human. The amino acid composition shows very little similarity to the human motif, which potentially contributes to differences in the innate immune response between species, as glycosylation across this rapidly evolving domain provides much of the musical barrier. Future studies of the function of MUC2 in the innate immune response system in chicken could provide an important model organism to increase our understanding of the biological significance of MUC2 in host defense and highlight the potential of the chicken for creating new immune-based therapies.
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spelling pubmed-35499772013-01-24 Cloning, Annotation and Developmental Expression of the Chicken Intestinal MUC2 Gene Jiang, Zhengyu Applegate, Todd J. Lossie, Amy C. PLoS One Research Article Intestinal mucin 2 (MUC2) encodes a heavily glycosylated, gel-forming mucin, which creates an important protective mucosal layer along the gastrointestinal tract in humans and other species. This first line of defense guards against attacks from microorganisms and is integral to the innate immune system. As a first step towards characterizing the innate immune response of MUC2 in different species, we report the cloning of a full-length, 11,359 bp chicken MUC2 cDNA, and describe the genomic organization and functional annotation of this complex, 74.5 kb locus. MUC2 contains 64 exons and demonstrates distinct spatiotemporal expression profiles throughout development in the gastrointestinal tract; expression increases with gestational age and from anterior to posterior along the gut. The chicken protein has a similar domain organization as the human orthologue, with a signal peptide and several von Willebrand domains in the N-terminus and the characteristic cystine knot at the C-terminus. The PTS domain of the chicken MUC2 protein spans ∼1600 amino acids and is interspersed with four CysD motifs. However, the PTS domain in the chicken diverges significantly from the human orthologue; although the chicken domain is shorter, the repetitive unit is 69 amino acids in length, which is three times longer than the human. The amino acid composition shows very little similarity to the human motif, which potentially contributes to differences in the innate immune response between species, as glycosylation across this rapidly evolving domain provides much of the musical barrier. Future studies of the function of MUC2 in the innate immune response system in chicken could provide an important model organism to increase our understanding of the biological significance of MUC2 in host defense and highlight the potential of the chicken for creating new immune-based therapies. Public Library of Science 2013-01-21 /pmc/articles/PMC3549977/ /pubmed/23349743 http://dx.doi.org/10.1371/journal.pone.0053781 Text en © 2013 Jiang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jiang, Zhengyu
Applegate, Todd J.
Lossie, Amy C.
Cloning, Annotation and Developmental Expression of the Chicken Intestinal MUC2 Gene
title Cloning, Annotation and Developmental Expression of the Chicken Intestinal MUC2 Gene
title_full Cloning, Annotation and Developmental Expression of the Chicken Intestinal MUC2 Gene
title_fullStr Cloning, Annotation and Developmental Expression of the Chicken Intestinal MUC2 Gene
title_full_unstemmed Cloning, Annotation and Developmental Expression of the Chicken Intestinal MUC2 Gene
title_short Cloning, Annotation and Developmental Expression of the Chicken Intestinal MUC2 Gene
title_sort cloning, annotation and developmental expression of the chicken intestinal muc2 gene
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549977/
https://www.ncbi.nlm.nih.gov/pubmed/23349743
http://dx.doi.org/10.1371/journal.pone.0053781
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