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Context-dependent enhancer function revealed by targeted inter-TAD relocation

The expression of some genes depends on large, adjacent regions of the genome that contain multiple enhancers. These regulatory landscapes frequently align with Topologically Associating Domains (TADs), where they integrate the function of multiple similar enhancers to produce a global, TAD-specific...

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Autores principales: Bolt, Christopher Chase, Lopez-Delisle, Lucille, Hintermann, Aurélie, Mascrez, Bénédicte, Rauseo, Antonella, Andrey, Guillaume, Duboule, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205857/
https://www.ncbi.nlm.nih.gov/pubmed/35715427
http://dx.doi.org/10.1038/s41467-022-31241-3
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author Bolt, Christopher Chase
Lopez-Delisle, Lucille
Hintermann, Aurélie
Mascrez, Bénédicte
Rauseo, Antonella
Andrey, Guillaume
Duboule, Denis
author_facet Bolt, Christopher Chase
Lopez-Delisle, Lucille
Hintermann, Aurélie
Mascrez, Bénédicte
Rauseo, Antonella
Andrey, Guillaume
Duboule, Denis
author_sort Bolt, Christopher Chase
collection PubMed
description The expression of some genes depends on large, adjacent regions of the genome that contain multiple enhancers. These regulatory landscapes frequently align with Topologically Associating Domains (TADs), where they integrate the function of multiple similar enhancers to produce a global, TAD-specific regulation. We asked if an individual enhancer could overcome the influence of one of these landscapes, to drive gene transcription. To test this, we transferred an enhancer from its native location, into a nearby TAD with a related yet different functional specificity. We used the biphasic regulation of Hoxd genes during limb development as a paradigm. These genes are first activated in proximal limb cells by enhancers located in one TAD, which is then silenced when the neighboring TAD activates its enhancers in distal limb cells. We transferred a distal limb enhancer into the proximal limb TAD and found that its new context suppresses its normal distal specificity, even though it is bound by HOX13 transcription factors, which are responsible for the distal activity. This activity can be rescued only when a large portion of the surrounding environment is removed. These results indicate that, at least in some cases, the functioning of enhancer elements is subordinated to the host chromatin context, which can exert a dominant control over its activity.
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spelling pubmed-92058572022-06-19 Context-dependent enhancer function revealed by targeted inter-TAD relocation Bolt, Christopher Chase Lopez-Delisle, Lucille Hintermann, Aurélie Mascrez, Bénédicte Rauseo, Antonella Andrey, Guillaume Duboule, Denis Nat Commun Article The expression of some genes depends on large, adjacent regions of the genome that contain multiple enhancers. These regulatory landscapes frequently align with Topologically Associating Domains (TADs), where they integrate the function of multiple similar enhancers to produce a global, TAD-specific regulation. We asked if an individual enhancer could overcome the influence of one of these landscapes, to drive gene transcription. To test this, we transferred an enhancer from its native location, into a nearby TAD with a related yet different functional specificity. We used the biphasic regulation of Hoxd genes during limb development as a paradigm. These genes are first activated in proximal limb cells by enhancers located in one TAD, which is then silenced when the neighboring TAD activates its enhancers in distal limb cells. We transferred a distal limb enhancer into the proximal limb TAD and found that its new context suppresses its normal distal specificity, even though it is bound by HOX13 transcription factors, which are responsible for the distal activity. This activity can be rescued only when a large portion of the surrounding environment is removed. These results indicate that, at least in some cases, the functioning of enhancer elements is subordinated to the host chromatin context, which can exert a dominant control over its activity. Nature Publishing Group UK 2022-06-17 /pmc/articles/PMC9205857/ /pubmed/35715427 http://dx.doi.org/10.1038/s41467-022-31241-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bolt, Christopher Chase
Lopez-Delisle, Lucille
Hintermann, Aurélie
Mascrez, Bénédicte
Rauseo, Antonella
Andrey, Guillaume
Duboule, Denis
Context-dependent enhancer function revealed by targeted inter-TAD relocation
title Context-dependent enhancer function revealed by targeted inter-TAD relocation
title_full Context-dependent enhancer function revealed by targeted inter-TAD relocation
title_fullStr Context-dependent enhancer function revealed by targeted inter-TAD relocation
title_full_unstemmed Context-dependent enhancer function revealed by targeted inter-TAD relocation
title_short Context-dependent enhancer function revealed by targeted inter-TAD relocation
title_sort context-dependent enhancer function revealed by targeted inter-tad relocation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205857/
https://www.ncbi.nlm.nih.gov/pubmed/35715427
http://dx.doi.org/10.1038/s41467-022-31241-3
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