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Complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression

To gain insight into how mammalian gene expression is controlled by rapidly evolving regulatory elements, we jointly analysed promoter and enhancer activity with downstream transcription levels in liver samples from fifteen species. Genes associated with complex regulatory landscapes generally exhib...

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Detalles Bibliográficos
Autores principales: Berthelot, Camille, Villar, Diego, Horvath, Julie E., Odom, Duncan T., Flicek, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733139/
https://www.ncbi.nlm.nih.gov/pubmed/29180706
http://dx.doi.org/10.1038/s41559-017-0377-2
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author Berthelot, Camille
Villar, Diego
Horvath, Julie E.
Odom, Duncan T.
Flicek, Paul
author_facet Berthelot, Camille
Villar, Diego
Horvath, Julie E.
Odom, Duncan T.
Flicek, Paul
author_sort Berthelot, Camille
collection PubMed
description To gain insight into how mammalian gene expression is controlled by rapidly evolving regulatory elements, we jointly analysed promoter and enhancer activity with downstream transcription levels in liver samples from fifteen species. Genes associated with complex regulatory landscapes generally exhibit high expression levels that remain evolutionarily stable. While the number of regulatory elements is the key driver of transcriptional output and resilience, regulatory conservation matters: elements active across mammals most effectively stabilise gene expression. In contrast, recently-evolved enhancers typically contribute weakly, consistent with their high evolutionary plasticity. These effects are observed across the entire mammalian clade and robust to potential confounders, such as gene expression level. Using liver as a representative somatic tissue, our results illuminate how the evolutionary stability of gene expression is profoundly entwined with both the number and conservation of surrounding promoters and enhancers.
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spelling pubmed-57331392018-05-27 Complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression Berthelot, Camille Villar, Diego Horvath, Julie E. Odom, Duncan T. Flicek, Paul Nat Ecol Evol Article To gain insight into how mammalian gene expression is controlled by rapidly evolving regulatory elements, we jointly analysed promoter and enhancer activity with downstream transcription levels in liver samples from fifteen species. Genes associated with complex regulatory landscapes generally exhibit high expression levels that remain evolutionarily stable. While the number of regulatory elements is the key driver of transcriptional output and resilience, regulatory conservation matters: elements active across mammals most effectively stabilise gene expression. In contrast, recently-evolved enhancers typically contribute weakly, consistent with their high evolutionary plasticity. These effects are observed across the entire mammalian clade and robust to potential confounders, such as gene expression level. Using liver as a representative somatic tissue, our results illuminate how the evolutionary stability of gene expression is profoundly entwined with both the number and conservation of surrounding promoters and enhancers. 2017-11-27 2018-01 /pmc/articles/PMC5733139/ /pubmed/29180706 http://dx.doi.org/10.1038/s41559-017-0377-2 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Berthelot, Camille
Villar, Diego
Horvath, Julie E.
Odom, Duncan T.
Flicek, Paul
Complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression
title Complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression
title_full Complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression
title_fullStr Complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression
title_full_unstemmed Complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression
title_short Complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression
title_sort complexity and conservation of regulatory landscapes underlie evolutionary resilience of mammalian gene expression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733139/
https://www.ncbi.nlm.nih.gov/pubmed/29180706
http://dx.doi.org/10.1038/s41559-017-0377-2
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