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Uncoupling evolutionary changes in DNA sequence, transcription factor occupancy and enhancer activity
Sequence variation within enhancers plays a major role in both evolution and disease, yet its functional impact on transcription factor (TF) occupancy and enhancer activity remains poorly understood. Here, we assayed the binding of five essential TFs over multiple stages of embryogenesis in two dist...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550276/ https://www.ncbi.nlm.nih.gov/pubmed/28792889 http://dx.doi.org/10.7554/eLife.28440 |
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author | Khoueiry, Pierre Girardot, Charles Ciglar, Lucia Peng, Pei-Chen Gustafson, E Hilary Sinha, Saurabh Furlong, Eileen EM |
author_facet | Khoueiry, Pierre Girardot, Charles Ciglar, Lucia Peng, Pei-Chen Gustafson, E Hilary Sinha, Saurabh Furlong, Eileen EM |
author_sort | Khoueiry, Pierre |
collection | PubMed |
description | Sequence variation within enhancers plays a major role in both evolution and disease, yet its functional impact on transcription factor (TF) occupancy and enhancer activity remains poorly understood. Here, we assayed the binding of five essential TFs over multiple stages of embryogenesis in two distant Drosophila species (with 1.4 substitutions per neutral site), identifying thousands of orthologous enhancers with conserved or diverged combinatorial occupancy. We used these binding signatures to dissect two properties of developmental enhancers: (1) potential TF cooperativity, using signatures of co-associations and co-divergence in TF occupancy. This revealed conserved combinatorial binding despite sequence divergence, suggesting protein-protein interactions sustain conserved collective occupancy. (2) Enhancer in-vivo activity, revealing orthologous enhancers with conserved activity despite divergence in TF occupancy. Taken together, we identify enhancers with diverged motifs yet conserved occupancy and others with diverged occupancy yet conserved activity, emphasising the need to functionally measure the effect of divergence on enhancer activity. DOI: http://dx.doi.org/10.7554/eLife.28440.001 |
format | Online Article Text |
id | pubmed-5550276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-55502762017-08-11 Uncoupling evolutionary changes in DNA sequence, transcription factor occupancy and enhancer activity Khoueiry, Pierre Girardot, Charles Ciglar, Lucia Peng, Pei-Chen Gustafson, E Hilary Sinha, Saurabh Furlong, Eileen EM eLife Genes and Chromosomes Sequence variation within enhancers plays a major role in both evolution and disease, yet its functional impact on transcription factor (TF) occupancy and enhancer activity remains poorly understood. Here, we assayed the binding of five essential TFs over multiple stages of embryogenesis in two distant Drosophila species (with 1.4 substitutions per neutral site), identifying thousands of orthologous enhancers with conserved or diverged combinatorial occupancy. We used these binding signatures to dissect two properties of developmental enhancers: (1) potential TF cooperativity, using signatures of co-associations and co-divergence in TF occupancy. This revealed conserved combinatorial binding despite sequence divergence, suggesting protein-protein interactions sustain conserved collective occupancy. (2) Enhancer in-vivo activity, revealing orthologous enhancers with conserved activity despite divergence in TF occupancy. Taken together, we identify enhancers with diverged motifs yet conserved occupancy and others with diverged occupancy yet conserved activity, emphasising the need to functionally measure the effect of divergence on enhancer activity. DOI: http://dx.doi.org/10.7554/eLife.28440.001 eLife Sciences Publications, Ltd 2017-08-09 /pmc/articles/PMC5550276/ /pubmed/28792889 http://dx.doi.org/10.7554/eLife.28440 Text en © 2017, Khoueiry et al 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 | Genes and Chromosomes Khoueiry, Pierre Girardot, Charles Ciglar, Lucia Peng, Pei-Chen Gustafson, E Hilary Sinha, Saurabh Furlong, Eileen EM Uncoupling evolutionary changes in DNA sequence, transcription factor occupancy and enhancer activity |
title | Uncoupling evolutionary changes in DNA sequence, transcription factor occupancy and enhancer activity |
title_full | Uncoupling evolutionary changes in DNA sequence, transcription factor occupancy and enhancer activity |
title_fullStr | Uncoupling evolutionary changes in DNA sequence, transcription factor occupancy and enhancer activity |
title_full_unstemmed | Uncoupling evolutionary changes in DNA sequence, transcription factor occupancy and enhancer activity |
title_short | Uncoupling evolutionary changes in DNA sequence, transcription factor occupancy and enhancer activity |
title_sort | uncoupling evolutionary changes in dna sequence, transcription factor occupancy and enhancer activity |
topic | Genes and Chromosomes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550276/ https://www.ncbi.nlm.nih.gov/pubmed/28792889 http://dx.doi.org/10.7554/eLife.28440 |
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