多细胞生物
生物
染色质
增强子
转录因子
细胞命运测定
转录调控
计算生物学
基因表达调控
发起人
遗传学
基因
嘉雅宠物
核小体
细胞生物学
基因表达
作者
Sergio Espínola,Markus Götz,Maëlle Bellec,Olivier Messina,Jean-Bernard Fiche,Christophe Houbron,Matthieu Dejean,Ingolf Reim,Andrés M. Cardozo Gizzi,Mounia Lagha,Marcelo Nöllmann
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2021-04-01
卷期号:53 (4): 477-486
被引量:172
标识
DOI:10.1038/s41588-021-00816-z
摘要
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.
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