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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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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. |
format | Online Article Text |
id | pubmed-5733139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
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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