Assessment of the Epigenomic Landscape in Human Myometrium at Term Pregnancy

The myometrium plays a critical component during pregnancy. It is responsible for the uterus’ structural integrity and force generation at term, Emerging studies in mice indicate a dynamic change of the myometrial epigenome and transcriptome during pregnancy to ready the contractile machinery for parturition. However, the regulatory systems underlying myometrial gene expression patterns throughout gestation remain largely unknown. Here we investigated the human term pregnant nonlabor myometrial biopsies for transcriptome, enhancer histone mark cistrome, and chromatin conformation pattern mapping. More than thirty-thousand putative enhancers with H3K27ac and H3K4me1 double positive marks were identified in the myometrium. Enriched transcription factor binding motifs include known myometrial regulators AP-1, STAT, NFkB, and PGR among others. Putative myometrial super enhancers are mostly colocalized with progesterone receptor occupying sites and preferentially associated with highly expressing genes, suggesting a conserved role of PGR in regulating the myometrial transcriptome between species. In human myometrial specimens, inferred PGR activities are positively correlated withPLCL2mRNA levels, supporting that PGR may act through this genomic region to promotePLCL2expression. PGR overexpression facilitatedPLCL2gene expression in myometrial cells Using CRISPR activation the functionality of a PGR putative enhancer 35-kilobases upstream of the contractile-restrictive genePLCL2. In summary, results of this study serve as a resource to study gene regulatory mechanisms in the human myometrium at the term pregnancy stage for further advancing women’s health research.