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Insights into the Evolution of the Suppressors of Cytokine Signaling (SOCS) Gene Family in Vertebrates
The SOCS family are key negative regulators of cytokine and growth factor signaling. Typically, 8–17 SOCS genes are present in vertebrate species with eight known in mammals, classified as type I (SOCS4–7) and type II (CISH and SOCS1–3) SOCS. It was believed that the type II SOCS were expanded throu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368001/ https://www.ncbi.nlm.nih.gov/pubmed/30521052 http://dx.doi.org/10.1093/molbev/msy230 |
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author | Wang, Bei Wangkahart, Eakapol Secombes, Christopher J Wang, Tiehui |
author_facet | Wang, Bei Wangkahart, Eakapol Secombes, Christopher J Wang, Tiehui |
author_sort | Wang, Bei |
collection | PubMed |
description | The SOCS family are key negative regulators of cytokine and growth factor signaling. Typically, 8–17 SOCS genes are present in vertebrate species with eight known in mammals, classified as type I (SOCS4–7) and type II (CISH and SOCS1–3) SOCS. It was believed that the type II SOCS were expanded through the two rounds of whole genome duplication (1R and 2R WGDs) from a single CISH/SOCS1–3 precursor. Previously, 12 genes were identified in rainbow trout but here we report 15 additional loci are present, and confirm 26 of the genes are expressed, giving rainbow trout the largest SOCS gene repertoire identified to date. The discovery of the additional SOCS genes in trout has led to a novel model of SOCS family evolution, whereby the vertebrate SOCS gene family was derived from CISH/SOCS2, SOCS1/SOCS3, SOCS4/5, SOCS6, and SOCS7 ancestors likely present before the two WGD events. It is also apparent that teleost SOCS2b, SOCS4, and SOCS5b molecules are not true orthologues of mammalian SOCS2, SOCS4, and SOCS5, respectively. The rate of SOCS gene structural changes increased from 2R vertebrates, to 4R rainbow trout, and the genes with structural changes show large differences and low correlation coefficient of expression levels relative to their paralogues, suggesting a role of structural changes in expression and functional diversification. This study has important impacts in the functional prediction and understanding of the SOCS gene family in different vertebrates, and provides a framework for determining how many SOCS genes could be expected in a particular vertebrate species/lineage. |
format | Online Article Text |
id | pubmed-6368001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63680012019-02-20 Insights into the Evolution of the Suppressors of Cytokine Signaling (SOCS) Gene Family in Vertebrates Wang, Bei Wangkahart, Eakapol Secombes, Christopher J Wang, Tiehui Mol Biol Evol Discoveries The SOCS family are key negative regulators of cytokine and growth factor signaling. Typically, 8–17 SOCS genes are present in vertebrate species with eight known in mammals, classified as type I (SOCS4–7) and type II (CISH and SOCS1–3) SOCS. It was believed that the type II SOCS were expanded through the two rounds of whole genome duplication (1R and 2R WGDs) from a single CISH/SOCS1–3 precursor. Previously, 12 genes were identified in rainbow trout but here we report 15 additional loci are present, and confirm 26 of the genes are expressed, giving rainbow trout the largest SOCS gene repertoire identified to date. The discovery of the additional SOCS genes in trout has led to a novel model of SOCS family evolution, whereby the vertebrate SOCS gene family was derived from CISH/SOCS2, SOCS1/SOCS3, SOCS4/5, SOCS6, and SOCS7 ancestors likely present before the two WGD events. It is also apparent that teleost SOCS2b, SOCS4, and SOCS5b molecules are not true orthologues of mammalian SOCS2, SOCS4, and SOCS5, respectively. The rate of SOCS gene structural changes increased from 2R vertebrates, to 4R rainbow trout, and the genes with structural changes show large differences and low correlation coefficient of expression levels relative to their paralogues, suggesting a role of structural changes in expression and functional diversification. This study has important impacts in the functional prediction and understanding of the SOCS gene family in different vertebrates, and provides a framework for determining how many SOCS genes could be expected in a particular vertebrate species/lineage. Oxford University Press 2019-02 2018-12-05 /pmc/articles/PMC6368001/ /pubmed/30521052 http://dx.doi.org/10.1093/molbev/msy230 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Wang, Bei Wangkahart, Eakapol Secombes, Christopher J Wang, Tiehui Insights into the Evolution of the Suppressors of Cytokine Signaling (SOCS) Gene Family in Vertebrates |
title | Insights into the Evolution of the Suppressors of Cytokine Signaling (SOCS) Gene Family in Vertebrates |
title_full | Insights into the Evolution of the Suppressors of Cytokine Signaling (SOCS) Gene Family in Vertebrates |
title_fullStr | Insights into the Evolution of the Suppressors of Cytokine Signaling (SOCS) Gene Family in Vertebrates |
title_full_unstemmed | Insights into the Evolution of the Suppressors of Cytokine Signaling (SOCS) Gene Family in Vertebrates |
title_short | Insights into the Evolution of the Suppressors of Cytokine Signaling (SOCS) Gene Family in Vertebrates |
title_sort | insights into the evolution of the suppressors of cytokine signaling (socs) gene family in vertebrates |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368001/ https://www.ncbi.nlm.nih.gov/pubmed/30521052 http://dx.doi.org/10.1093/molbev/msy230 |
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