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Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements
Transposable elements (TEs) allow rewiring of regulatory networks, and the recent amplification of the ISX element dispersed 77 functional but suboptimal binding sites for the dosage compensation complex to a newly formed X chromosome in Drosophila. Here we identify two linked refining mutations wit...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384637/ https://www.ncbi.nlm.nih.gov/pubmed/25688566 http://dx.doi.org/10.7554/eLife.05899 |
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author | Ellison, Christopher E Bachtrog, Doris |
author_facet | Ellison, Christopher E Bachtrog, Doris |
author_sort | Ellison, Christopher E |
collection | PubMed |
description | Transposable elements (TEs) allow rewiring of regulatory networks, and the recent amplification of the ISX element dispersed 77 functional but suboptimal binding sites for the dosage compensation complex to a newly formed X chromosome in Drosophila. Here we identify two linked refining mutations within ISX that interact epistatically to increase binding affinity to the dosage compensation complex. Selection has increased the frequency of this derived haplotype in the population, which is fixed at 30% of ISX insertions and polymorphic among another 41%. Sharing of this haplotype indicates that high levels of gene conversion among ISX elements allow them to ‘crowd-source’ refining mutations, and a refining mutation that occurs at any single ISX element can spread in two dimensions: horizontally across insertion sites by non-allelic gene conversion, and vertically through the population by natural selection. These results describe a novel route by which fully functional regulatory elements can arise rapidly from TEs and implicate non-allelic gene conversion as having an important role in accelerating the evolutionary fine-tuning of regulatory networks. DOI: http://dx.doi.org/10.7554/eLife.05899.001 |
format | Online Article Text |
id | pubmed-4384637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43846372015-04-07 Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements Ellison, Christopher E Bachtrog, Doris eLife Genomics and Evolutionary Biology Transposable elements (TEs) allow rewiring of regulatory networks, and the recent amplification of the ISX element dispersed 77 functional but suboptimal binding sites for the dosage compensation complex to a newly formed X chromosome in Drosophila. Here we identify two linked refining mutations within ISX that interact epistatically to increase binding affinity to the dosage compensation complex. Selection has increased the frequency of this derived haplotype in the population, which is fixed at 30% of ISX insertions and polymorphic among another 41%. Sharing of this haplotype indicates that high levels of gene conversion among ISX elements allow them to ‘crowd-source’ refining mutations, and a refining mutation that occurs at any single ISX element can spread in two dimensions: horizontally across insertion sites by non-allelic gene conversion, and vertically through the population by natural selection. These results describe a novel route by which fully functional regulatory elements can arise rapidly from TEs and implicate non-allelic gene conversion as having an important role in accelerating the evolutionary fine-tuning of regulatory networks. DOI: http://dx.doi.org/10.7554/eLife.05899.001 eLife Sciences Publications, Ltd 2015-02-17 /pmc/articles/PMC4384637/ /pubmed/25688566 http://dx.doi.org/10.7554/eLife.05899 Text en © 2015, Ellison and Bachtrog http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genomics and Evolutionary Biology Ellison, Christopher E Bachtrog, Doris Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements |
title | Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements |
title_full | Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements |
title_fullStr | Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements |
title_full_unstemmed | Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements |
title_short | Non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements |
title_sort | non-allelic gene conversion enables rapid evolutionary change at multiple regulatory sites encoded by transposable elements |
topic | Genomics and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384637/ https://www.ncbi.nlm.nih.gov/pubmed/25688566 http://dx.doi.org/10.7554/eLife.05899 |
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