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The evolution of S100A7: an unusual gene expansion in Myotis bats

BACKGROUND: The S100A7 gene, also called psoriasin, was first described as an upregulated protein in psoriatic skin. For the past years, the importance of this protein as a key effector of innate immunity has been clearly established, not only due to its importance protecting against bacteria skin i...

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Autores principales: Águeda-Pinto, Ana, Castro, L. Filipe C., Esteves, Pedro J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518696/
https://www.ncbi.nlm.nih.gov/pubmed/31088346
http://dx.doi.org/10.1186/s12862-019-1433-0
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author Águeda-Pinto, Ana
Castro, L. Filipe C.
Esteves, Pedro J.
author_facet Águeda-Pinto, Ana
Castro, L. Filipe C.
Esteves, Pedro J.
author_sort Águeda-Pinto, Ana
collection PubMed
description BACKGROUND: The S100A7 gene, also called psoriasin, was first described as an upregulated protein in psoriatic skin. For the past years, the importance of this protein as a key effector of innate immunity has been clearly established, not only due to its importance protecting against bacteria skin insult in humans, but also because of its important role in amplifying inflammatory processes. Given the importance of S100A7 in host defense, S100A7 genes have been mostly studied in humans. Here we provide a detailed analysis of the evolution of the gene family encoding for the S100A7 protein in mammals. RESULTS: Examination of several mammalian genomes revealed an unexpected variation in the copy number of S100A7. Among the most representative mammalian groups, we report that multiple events of duplication, gene loss and high mutation rates are shaping the evolution of this gene family. An unexpected result comes from Myotis species (order Chiroptera), where we found an outstanding S100A7 gene radiation, resulting in more than 10 copies in M. lucifugus and 5 copies in M. brandtii. These findings suggest a unique adaptive road in these species and are suggestive of special role of this protein in their immune system. CONCLUSIONS: We found different evolutionary histories among different mammalian groups. Overall, our results suggest that this gene family is evolving under the birth-and-death model of evolution. To our knowledge, this work represents the first detailed analysis of phylogenetic relationships of S100A7 within mammals and therefore will pave the way to further clarify their unique function in the immune system. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1433-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-65186962019-05-21 The evolution of S100A7: an unusual gene expansion in Myotis bats Águeda-Pinto, Ana Castro, L. Filipe C. Esteves, Pedro J. BMC Evol Biol Research Article BACKGROUND: The S100A7 gene, also called psoriasin, was first described as an upregulated protein in psoriatic skin. For the past years, the importance of this protein as a key effector of innate immunity has been clearly established, not only due to its importance protecting against bacteria skin insult in humans, but also because of its important role in amplifying inflammatory processes. Given the importance of S100A7 in host defense, S100A7 genes have been mostly studied in humans. Here we provide a detailed analysis of the evolution of the gene family encoding for the S100A7 protein in mammals. RESULTS: Examination of several mammalian genomes revealed an unexpected variation in the copy number of S100A7. Among the most representative mammalian groups, we report that multiple events of duplication, gene loss and high mutation rates are shaping the evolution of this gene family. An unexpected result comes from Myotis species (order Chiroptera), where we found an outstanding S100A7 gene radiation, resulting in more than 10 copies in M. lucifugus and 5 copies in M. brandtii. These findings suggest a unique adaptive road in these species and are suggestive of special role of this protein in their immune system. CONCLUSIONS: We found different evolutionary histories among different mammalian groups. Overall, our results suggest that this gene family is evolving under the birth-and-death model of evolution. To our knowledge, this work represents the first detailed analysis of phylogenetic relationships of S100A7 within mammals and therefore will pave the way to further clarify their unique function in the immune system. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1433-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-14 /pmc/articles/PMC6518696/ /pubmed/31088346 http://dx.doi.org/10.1186/s12862-019-1433-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Águeda-Pinto, Ana
Castro, L. Filipe C.
Esteves, Pedro J.
The evolution of S100A7: an unusual gene expansion in Myotis bats
title The evolution of S100A7: an unusual gene expansion in Myotis bats
title_full The evolution of S100A7: an unusual gene expansion in Myotis bats
title_fullStr The evolution of S100A7: an unusual gene expansion in Myotis bats
title_full_unstemmed The evolution of S100A7: an unusual gene expansion in Myotis bats
title_short The evolution of S100A7: an unusual gene expansion in Myotis bats
title_sort evolution of s100a7: an unusual gene expansion in myotis bats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518696/
https://www.ncbi.nlm.nih.gov/pubmed/31088346
http://dx.doi.org/10.1186/s12862-019-1433-0
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