bioRxiv · 10.1101/2024.06.12.598713
Regeneration-specific promoter switching facilitates Mest expression in the mouse digit tip to modulate neutrophil response
Abstract
The mouse digit tip regenerates following amputation, a process mediated by a cellularly heterogeneous blastema. We previously found the gene Mest to be highly expressed in mesenchymal cells of the blastema and a strong candidate pro-regenerative gene. We now show Mest digit expression is regeneration-specific and not upregulated in post-amputation fibrosing proximal digits. Mest homozygous knockout mice exhibit delayed bone regeneration though no phenotype is found in paternal knockout mice, inconsistent with the defined maternal genomic imprinting of Mest. We demonstrate that promoter switching, not loss of imprinting, regulates biallelic Mest expression in the blastema and does not occur during embryogenesis, indicating a regeneration-specific mechanism. Requirement for Mest expression is tied to modulating neutrophil response, as revealed by scRNAseq and FACS comparing wildtype and knockout blastemas. Collectively, the imprinted gene Mest is required for proper digit tip regeneration and its blastema expression is facilitated by promoter switching for biallelic expression.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Jou, V., Pena, S. M., Lehoczky, J. A.. 2024-06-15. Regeneration-specific promoter switching facilitates Mest expression in the mouse digit tip to modulate neutrophil response. https://doi.org/10.1101/2024.06.12.598713
Cite the original work for its findings. Save a collection to share your selection of sources.