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Searching the Evolutionary Origin of Epithelial Mucus Protein Components—Mucins and FCGBP

The gel-forming mucins are large glycosylated proteins that are essential components of the mucus layers covering epithelial cells. Using novel methods of identifying mucins based on profile hidden Markov models, we have found a large number of such proteins in Metazoa, aiding in their classificatio...

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Detalles Bibliográficos
Autores principales: Lang, Tiange, Klasson, Sofia, Larsson, Erik, Johansson, Malin E. V., Hansson, Gunnar C., Samuelsson, Tore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948705/
https://www.ncbi.nlm.nih.gov/pubmed/27189557
http://dx.doi.org/10.1093/molbev/msw066
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author Lang, Tiange
Klasson, Sofia
Larsson, Erik
Johansson, Malin E. V.
Hansson, Gunnar C.
Samuelsson, Tore
author_facet Lang, Tiange
Klasson, Sofia
Larsson, Erik
Johansson, Malin E. V.
Hansson, Gunnar C.
Samuelsson, Tore
author_sort Lang, Tiange
collection PubMed
description The gel-forming mucins are large glycosylated proteins that are essential components of the mucus layers covering epithelial cells. Using novel methods of identifying mucins based on profile hidden Markov models, we have found a large number of such proteins in Metazoa, aiding in their classification and allowing evolutionary studies. Most vertebrates have 5–6 gel-forming mucin genes and the genomic arrangement of these genes is well conserved throughout vertebrates. An exception is the frog Xenopus tropicalis with an expanded repertoire of at least 26 mucins of this type. Furthermore, we found that the ovomucin protein, originally identified in chicken, is characteristic of reptiles, birds, and amphibians. Muc6 is absent in teleost fish, but we now show that it is present in animals such as ghost sharks, demonstrating an early origin in vertebrate evolution. Public RNA-Seq data were analyzed with respect to mucins in zebrafish, frog, and chicken, thus allowing comparison in regard of tissue and developmental specificity. Analyses of invertebrate proteins reveal that gel-forming-mucin type of proteins is widely distributed also in this group. Their presence in Cnidaria, Porifera, and in Ctenophora (comb jellies) shows that these proteins were present early in metazoan evolution. Finally, we examined the evolution of the FCGBP protein, abundant in mucus and related to gel-forming mucins in terms of structure and localization. We demonstrate that FCGBP, ubiquitous in vertebrates, has a conserved N-terminal domain. Interestingly, this domain is also present as an N-terminal sequence in a number of bacterial proteins.
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spelling pubmed-49487052016-07-20 Searching the Evolutionary Origin of Epithelial Mucus Protein Components—Mucins and FCGBP Lang, Tiange Klasson, Sofia Larsson, Erik Johansson, Malin E. V. Hansson, Gunnar C. Samuelsson, Tore Mol Biol Evol Discoveries The gel-forming mucins are large glycosylated proteins that are essential components of the mucus layers covering epithelial cells. Using novel methods of identifying mucins based on profile hidden Markov models, we have found a large number of such proteins in Metazoa, aiding in their classification and allowing evolutionary studies. Most vertebrates have 5–6 gel-forming mucin genes and the genomic arrangement of these genes is well conserved throughout vertebrates. An exception is the frog Xenopus tropicalis with an expanded repertoire of at least 26 mucins of this type. Furthermore, we found that the ovomucin protein, originally identified in chicken, is characteristic of reptiles, birds, and amphibians. Muc6 is absent in teleost fish, but we now show that it is present in animals such as ghost sharks, demonstrating an early origin in vertebrate evolution. Public RNA-Seq data were analyzed with respect to mucins in zebrafish, frog, and chicken, thus allowing comparison in regard of tissue and developmental specificity. Analyses of invertebrate proteins reveal that gel-forming-mucin type of proteins is widely distributed also in this group. Their presence in Cnidaria, Porifera, and in Ctenophora (comb jellies) shows that these proteins were present early in metazoan evolution. Finally, we examined the evolution of the FCGBP protein, abundant in mucus and related to gel-forming mucins in terms of structure and localization. We demonstrate that FCGBP, ubiquitous in vertebrates, has a conserved N-terminal domain. Interestingly, this domain is also present as an N-terminal sequence in a number of bacterial proteins. Oxford University Press 2016-08 2016-04-04 /pmc/articles/PMC4948705/ /pubmed/27189557 http://dx.doi.org/10.1093/molbev/msw066 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Lang, Tiange
Klasson, Sofia
Larsson, Erik
Johansson, Malin E. V.
Hansson, Gunnar C.
Samuelsson, Tore
Searching the Evolutionary Origin of Epithelial Mucus Protein Components—Mucins and FCGBP
title Searching the Evolutionary Origin of Epithelial Mucus Protein Components—Mucins and FCGBP
title_full Searching the Evolutionary Origin of Epithelial Mucus Protein Components—Mucins and FCGBP
title_fullStr Searching the Evolutionary Origin of Epithelial Mucus Protein Components—Mucins and FCGBP
title_full_unstemmed Searching the Evolutionary Origin of Epithelial Mucus Protein Components—Mucins and FCGBP
title_short Searching the Evolutionary Origin of Epithelial Mucus Protein Components—Mucins and FCGBP
title_sort searching the evolutionary origin of epithelial mucus protein components—mucins and fcgbp
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948705/
https://www.ncbi.nlm.nih.gov/pubmed/27189557
http://dx.doi.org/10.1093/molbev/msw066
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