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Shadow Enhancers Are Pervasive Features of Developmental Regulatory Networks

Embryogenesis is remarkably robust to segregating mutations and environmental variation; under a range of conditions, embryos of a given species develop into stereotypically patterned organisms. Such robustness is thought to be conferred, in part, through elements within regulatory networks that per...

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Autores principales: Cannavò, Enrico, Khoueiry, Pierre, Garfield, David A., Geeleher, Paul, Zichner, Thomas, Gustafson, E. Hilary, Ciglar, Lucia, Korbel, Jan O., Furlong, Eileen E.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712172/
https://www.ncbi.nlm.nih.gov/pubmed/26687625
http://dx.doi.org/10.1016/j.cub.2015.11.034
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author Cannavò, Enrico
Khoueiry, Pierre
Garfield, David A.
Geeleher, Paul
Zichner, Thomas
Gustafson, E. Hilary
Ciglar, Lucia
Korbel, Jan O.
Furlong, Eileen E.M.
author_facet Cannavò, Enrico
Khoueiry, Pierre
Garfield, David A.
Geeleher, Paul
Zichner, Thomas
Gustafson, E. Hilary
Ciglar, Lucia
Korbel, Jan O.
Furlong, Eileen E.M.
author_sort Cannavò, Enrico
collection PubMed
description Embryogenesis is remarkably robust to segregating mutations and environmental variation; under a range of conditions, embryos of a given species develop into stereotypically patterned organisms. Such robustness is thought to be conferred, in part, through elements within regulatory networks that perform similar, redundant tasks. Redundant enhancers (or “shadow” enhancers), for example, can confer precision and robustness to gene expression, at least at individual, well-studied loci. However, the extent to which enhancer redundancy exists and can thereby have a major impact on developmental robustness remains unknown. Here, we systematically assessed this, identifying over 1,000 predicted shadow enhancers during Drosophila mesoderm development. The activity of 23 elements, associated with five genes, was examined in transgenic embryos, while natural structural variation among individuals was used to assess their ability to buffer against genetic variation. Our results reveal three clear properties of enhancer redundancy within developmental systems. First, it is much more pervasive than previously anticipated, with 64% of loci examined having shadow enhancers. Their spatial redundancy is often partial in nature, while the non-overlapping function may explain why these enhancers are maintained within a population. Second, over 70% of loci do not follow the simple situation of having only two shadow enhancers—often there are three (rols), four (CadN and ade5), or five (Traf1), at least one of which can be deleted with no obvious phenotypic effects. Third, although shadow enhancers can buffer variation, patterns of segregating variation suggest that they play a more complex role in development than generally considered.
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spelling pubmed-47121722016-02-11 Shadow Enhancers Are Pervasive Features of Developmental Regulatory Networks Cannavò, Enrico Khoueiry, Pierre Garfield, David A. Geeleher, Paul Zichner, Thomas Gustafson, E. Hilary Ciglar, Lucia Korbel, Jan O. Furlong, Eileen E.M. Curr Biol Article Embryogenesis is remarkably robust to segregating mutations and environmental variation; under a range of conditions, embryos of a given species develop into stereotypically patterned organisms. Such robustness is thought to be conferred, in part, through elements within regulatory networks that perform similar, redundant tasks. Redundant enhancers (or “shadow” enhancers), for example, can confer precision and robustness to gene expression, at least at individual, well-studied loci. However, the extent to which enhancer redundancy exists and can thereby have a major impact on developmental robustness remains unknown. Here, we systematically assessed this, identifying over 1,000 predicted shadow enhancers during Drosophila mesoderm development. The activity of 23 elements, associated with five genes, was examined in transgenic embryos, while natural structural variation among individuals was used to assess their ability to buffer against genetic variation. Our results reveal three clear properties of enhancer redundancy within developmental systems. First, it is much more pervasive than previously anticipated, with 64% of loci examined having shadow enhancers. Their spatial redundancy is often partial in nature, while the non-overlapping function may explain why these enhancers are maintained within a population. Second, over 70% of loci do not follow the simple situation of having only two shadow enhancers—often there are three (rols), four (CadN and ade5), or five (Traf1), at least one of which can be deleted with no obvious phenotypic effects. Third, although shadow enhancers can buffer variation, patterns of segregating variation suggest that they play a more complex role in development than generally considered. Cell Press 2016-01-11 /pmc/articles/PMC4712172/ /pubmed/26687625 http://dx.doi.org/10.1016/j.cub.2015.11.034 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cannavò, Enrico
Khoueiry, Pierre
Garfield, David A.
Geeleher, Paul
Zichner, Thomas
Gustafson, E. Hilary
Ciglar, Lucia
Korbel, Jan O.
Furlong, Eileen E.M.
Shadow Enhancers Are Pervasive Features of Developmental Regulatory Networks
title Shadow Enhancers Are Pervasive Features of Developmental Regulatory Networks
title_full Shadow Enhancers Are Pervasive Features of Developmental Regulatory Networks
title_fullStr Shadow Enhancers Are Pervasive Features of Developmental Regulatory Networks
title_full_unstemmed Shadow Enhancers Are Pervasive Features of Developmental Regulatory Networks
title_short Shadow Enhancers Are Pervasive Features of Developmental Regulatory Networks
title_sort shadow enhancers are pervasive features of developmental regulatory networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712172/
https://www.ncbi.nlm.nih.gov/pubmed/26687625
http://dx.doi.org/10.1016/j.cub.2015.11.034
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