Peroxisome proliferator-activated receptor \u03b3 (PPAR\u03b3), encoded by the PPARG<\/em> gene on chromosome 3p25.2 in humans, is a ligand-dependent transcription factor that belongs to the nuclear receptor family. In various tissues, PPAR\u03b3 controls cell differentiation, proliferation, or fusion. Its essential role in the development and functions of the placenta is now well established. To date, the specific functions of its RNA isoforms, encoded by ten exons, in trophoblast biology, including cell fusion and invasion, remain unknown. As translation is mainly regulated by the 5’UTR sequences of mature mRNA, this region was analyzed, and four previously unreported exonic sequences were revealed. Their expressions were confirmed and quantified in villous cytotrophoblasts from term placenta and in chorionic villi from both first-trimester and term placenta. Distinct expression patterns were observed: one exon showed weak expression in placental and chorionic cells, another exhibited stable expression throughout pregnancy, while two exons specific to villous cytotrophoblasts displayed increased expression during the first trimester, suggesting a role in oxygen-responsive mechanisms. Among these, one may be involved in villous trophoblast differentiation. These findings demonstrate that the PPARG<\/em> gene is composed of 14 exons and is highly regulated depending on cell type and the stage of cell differentiation.<\/p>\n\n\n\n Keywords:<\/strong> 5\u2032UTR exon; PPARG gene; cell-type-specific expression; placenta; pregnancy; trophoblast differentiation.<\/p>\n","protected":false},"excerpt":{"rendered":" Cells. 2026 Apr 1;15(7):639.<\/p>\n","protected":false},"featured_media":0,"template":"","class_list":["post-9332","publication","type-publication","status-publish","hentry"],"yoast_head":"\n