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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...

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Autores principales: Khoueiry, Pierre, Girardot, Charles, Ciglar, Lucia, Peng, Pei-Chen, Gustafson, E Hilary, Sinha, Saurabh, Furlong, Eileen EM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
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
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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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