Cis-regulatory chromatin loops arise before TADs and gene activation, and are independent of cell fate during early Drosophila development

Acquisition of cell fate is thought to rely on the specific interaction of remote cis -regulatory modules (CRMs), for example, enhancers and target promoters. However, the precise interplay between chromatin structure and gene expression is still unclear, particularly within multicellular developing...

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Published inNature genetics Vol. 53; no. 4; pp. 477 - 486
Main Authors Espinola, Sergio Martin, Götz, Markus, Bellec, Maelle, Messina, Olivier, Fiche, Jean-Bernard, Houbron, Christophe, Dejean, Matthieu, Reim, Ingolf, Cardozo Gizzi, Andrés M., Lagha, Mounia, Nollmann, Marcelo
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.04.2021
Nature Publishing Group
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Summary:Acquisition of cell fate is thought to rely on the specific interaction of remote cis -regulatory modules (CRMs), for example, enhancers and target promoters. However, the precise interplay between chromatin structure and gene expression is still unclear, particularly within multicellular developing organisms. In the present study, we employ Hi-M, a single-cell spatial genomics approach, to detect CRM–promoter looping interactions within topologically associating domains (TADs) during early Drosophila development. By comparing cis -regulatory loops in alternate cell types, we show that physical proximity does not necessarily instruct transcriptional states. Moreover, multi-way analyses reveal that multiple CRMs spatially coalesce to form hubs. Loops and CRM hubs are established early during development, before the emergence of TADs. Moreover, CRM hubs are formed, in part, via the action of the pioneer transcription factor Zelda and precede transcriptional activation. Our approach provides insight into the role of CRM–promoter interactions in defining transcriptional states, as well as distinct cell types. Single-cell analysis of Drosophila development with Hi-M suggests that physical proximity between regulatory regions does not necessarily instruct transcriptional states. Multi-way analyses identify the existence of regulatory hubs that emerge before topologically associating domains.
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ISSN:1061-4036
1546-1718
DOI:10.1038/s41588-021-00816-z