Enhancer-promoter interactions become more instructive in the transition from cell-fate specification to tissue differentiation.

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State: Public
Version: Final published version
License: CC BY 4.0
Serval ID
serval:BIB_129486315E31
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Enhancer-promoter interactions become more instructive in the transition from cell-fate specification to tissue differentiation.
Journal
Nature genetics
Author(s)
Pollex T., Rabinowitz A., Gambetta M.C., Marco-Ferreres R., Viales R.R., Jankowski A., Schaub C., Furlong EEM
ISSN
1546-1718 (Electronic)
ISSN-L
1061-4036
Publication state
In Press
Peer-reviewed
Oui
Language
english
Notes
Publication types: Journal Article
Publication Status: aheadofprint
Abstract
To regulate expression, enhancers must come in proximity to their target gene. However, the relationship between the timing of enhancer-promoter (E-P) proximity and activity remains unclear, with examples of uncoupled, anticorrelated and correlated interactions. To assess this, we selected 600 characterized enhancers or promoters with tissue-specific activity in Drosophila embryos and performed Capture-C in FACS-purified myogenic or neurogenic cells during specification and tissue differentiation. This enabled direct comparison between E-P proximity and activity transitioning from OFF-to-ON and ON-to-OFF states across developmental conditions. This showed remarkably similar E-P topologies between specified muscle and neuronal cells, which are uncoupled from activity. During tissue differentiation, many new distal interactions emerge where changes in E-P proximity reflect changes in activity. The mode of E-P regulation therefore appears to change as embryogenesis proceeds, from largely permissive topologies during cell-fate specification to more instructive regulation during terminal tissue differentiation, when E-P proximity is coupled to activation.
Pubmed
Web of science
Open Access
Yes
Create date
14/03/2024 18:15
Last modification date
26/03/2024 8:10
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