Organ‐Specific and Conserved Regulatory Logic Orchestrates Gene Expression in the Embryonic Mesothelium

Journal article

The embryonic coelomic mesothelium acts as a critical progenitor hub during mammalian organogenesis, undergoing epithelial‐to‐mesenchymal transition (EMT) to drive vascular growth and parenchymal development in visceral organs. A prominent example is the epicardium, which plays an essential role during heart development. The principles of gene regulation in the coelomic mesothelium remain poorly defined. Specifically, it is unclear how cis‐regulatory elements, including enhancers, orchestrate the spatiotemporal patterns of gene expression required for mesothelial identity and function. Here, a multi‐omic approach was used to identify trans‐ and cis‐regulatory elements that regulate mesothelial gene expression in three organs: heart, lung, and pancreas. This analysis uncovers a cardiac‐specific regulatory circuit in which the transcription factor (TF) TBX20 selectively activates epicardial enhancers to orchestrate essential developmental programs. In contrast, TF MAF orchestrates pan‐mesothelial gene expression via conserved CREs, which are absent in non‐mesothelial lineages. Our integrated genomic analysis reveals MAF as a central custodian of mesothelial identity, a role underscored by its negative correlation with EMT, evolutionary conservation, and dynamic regulatory activity throughout development. Our work establishes a foundational blueprint of the gene regulatory landscape governing the coelomic mesothelium, defining both conserved principles and organ‐specific mechanisms of spatiotemporal gene expression during early mammalian development.

Authors: Dang, QM; Smart, N; Redpath, AN; Vieira, JM

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Wiley
• Journal: Advanced Science
• Article number: e17640
• Publication date: 2026-04-03
• Acceptance date: 2026-03-26
• DOI: 10.1002/advs.202517640
• EISSN: 2198-3844
• ISSN: 2198-3844
• Language: English
• Keywords: epigenetics; in silico integration; embryogenesis; enhancers; multi‐omics; developmental biology; single‐cell genomics