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Corepressor diversification by alternative mRNA splicing is species specific
BACKGROUND: SMRT and NCoR are corepressor paralogs that help mediate transcriptional repression by a variety of transcription factors, including the nuclear hormone receptors. The functions of both corepressors are extensively diversified in mice by alternative mRNA splicing, generating a series of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069798/ https://www.ncbi.nlm.nih.gov/pubmed/27756201 http://dx.doi.org/10.1186/s12862-016-0781-2 |
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author | Privalsky, Martin L. Snyder, Chelsea A. Goodson, Michael L. |
author_facet | Privalsky, Martin L. Snyder, Chelsea A. Goodson, Michael L. |
author_sort | Privalsky, Martin L. |
collection | PubMed |
description | BACKGROUND: SMRT and NCoR are corepressor paralogs that help mediate transcriptional repression by a variety of transcription factors, including the nuclear hormone receptors. The functions of both corepressors are extensively diversified in mice by alternative mRNA splicing, generating a series of protein variants that differ in different tissues and that exert different, even diametrically opposite, biochemical and biological effects from one another. RESULTS: We report here that the alternative splicing previously reported for SMRT appears to be a relatively recent evolutionary phenomenon, with only one of these previously identified sites utilized in a teleost fish and a limited additional number of the additional known sites utilized in a bird, reptile, and marsupial. In contrast, extensive SMRT alternative splicing at these sites was detected among the placental mammals. The alternative splicing of NCoR previously identified in mice (and shown to regulate lipid and carbohydrate metabolism) is likely to have arisen separately and after that of SMRT, and includes an example of convergent evolution. CONCLUSIONS: We propose that the functions of both SMRT and NCoR have been diversified by alternative splicing during evolution to allow customization for different purposes in different tissues and different species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0781-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5069798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50697982016-10-24 Corepressor diversification by alternative mRNA splicing is species specific Privalsky, Martin L. Snyder, Chelsea A. Goodson, Michael L. BMC Evol Biol Research Article BACKGROUND: SMRT and NCoR are corepressor paralogs that help mediate transcriptional repression by a variety of transcription factors, including the nuclear hormone receptors. The functions of both corepressors are extensively diversified in mice by alternative mRNA splicing, generating a series of protein variants that differ in different tissues and that exert different, even diametrically opposite, biochemical and biological effects from one another. RESULTS: We report here that the alternative splicing previously reported for SMRT appears to be a relatively recent evolutionary phenomenon, with only one of these previously identified sites utilized in a teleost fish and a limited additional number of the additional known sites utilized in a bird, reptile, and marsupial. In contrast, extensive SMRT alternative splicing at these sites was detected among the placental mammals. The alternative splicing of NCoR previously identified in mice (and shown to regulate lipid and carbohydrate metabolism) is likely to have arisen separately and after that of SMRT, and includes an example of convergent evolution. CONCLUSIONS: We propose that the functions of both SMRT and NCoR have been diversified by alternative splicing during evolution to allow customization for different purposes in different tissues and different species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0781-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-19 /pmc/articles/PMC5069798/ /pubmed/27756201 http://dx.doi.org/10.1186/s12862-016-0781-2 Text en © The Author(s). 2016 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 Privalsky, Martin L. Snyder, Chelsea A. Goodson, Michael L. Corepressor diversification by alternative mRNA splicing is species specific |
title | Corepressor diversification by alternative mRNA splicing is species specific |
title_full | Corepressor diversification by alternative mRNA splicing is species specific |
title_fullStr | Corepressor diversification by alternative mRNA splicing is species specific |
title_full_unstemmed | Corepressor diversification by alternative mRNA splicing is species specific |
title_short | Corepressor diversification by alternative mRNA splicing is species specific |
title_sort | corepressor diversification by alternative mrna splicing is species specific |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069798/ https://www.ncbi.nlm.nih.gov/pubmed/27756201 http://dx.doi.org/10.1186/s12862-016-0781-2 |
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