{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Rosario FJ"],"funding":["Eunice Kennedy Shriver National Institute of Child Health and Human Development","NICHD NIH HHS","National Institute of Child Health and Human Development"],"pagination":["825-845"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12409993"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["139(14)"],"pubmed_abstract":["Abnormal fetal growth is associated with perinatal complications and adult disease. The placental mechanistic target of rapamycin (mTOR) signaling activity is positively correlated with placental nutrient transport and fetal growth. However, if this association represents a mechanistic link, it remains unknown. We hypothesized that trophoblast-specific Mtor knockdown in late pregnant mice decreases trophoblast nutrient transport and inhibits fetal growth. PiggyBac transposase-enhanced pronuclear injection was performed to generate transgenic mice containing a trophoblast-specific Cyp19I.1 promoter-driven, doxycycline-inducible luciferase reporter transgene with a Mtor shRNAmir sequence in its 3' untranslated region (UTR). We induced Mtor knockdown by administration of doxycycline starting "],"journal":["Clinical science (London, England : 1979)"],"pubmed_title":["PiggyBac transposase-mediated inducible trophoblast-specific knockdown of Mtor decreases placental nutrient transport and fetal growth."],"pmcid":["PMC12409993"],"funding_grant_id":["R01 HD105701","HD105701","R01 HD068370","HD068370"],"pubmed_authors":["Elston M","Jansson T","Razavy H","Urschitz J","Powell TL","Rosario FJ"],"additional_accession":[]},"is_claimable":false,"name":"PiggyBac transposase-mediated inducible trophoblast-specific knockdown of Mtor decreases placental nutrient transport and fetal growth.","description":"Abnormal fetal growth is associated with perinatal complications and adult disease. The placental mechanistic target of rapamycin (mTOR) signaling activity is positively correlated with placental nutrient transport and fetal growth. However, if this association represents a mechanistic link, it remains unknown. We hypothesized that trophoblast-specific Mtor knockdown in late pregnant mice decreases trophoblast nutrient transport and inhibits fetal growth. PiggyBac transposase-enhanced pronuclear injection was performed to generate transgenic mice containing a trophoblast-specific Cyp19I.1 promoter-driven, doxycycline-inducible luciferase reporter transgene with a Mtor shRNAmir sequence in its 3' untranslated region (UTR). We induced Mtor knockdown by administration of doxycycline starting ","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Jul","modification":"2026-05-29T22:05:48.615Z","creation":"2026-04-08T06:12:58.707Z"},"accession":"S-EPMC12409993","cross_references":{"pubmed":["40534504"],"doi":["10.1042/CS20243293"]}}