{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Xue L"],"funding":["Fundamental Research Funds for the Central Universities","National Natural Science Foundation of China","Qinglan Project of Jiangsu Province of China"],"pagination":["e54132"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9253765"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["23(7)"],"pubmed_abstract":["Our knowledge of the coordination of intergenerational inheritance and offspring metabolic reprogramming by gastrointestinal endocrine factors is largely unknown. Here, we showed that secretin (SCT), a brain-gut peptide, is downregulated by overnutrition in pregnant mice and women. More importantly, genetic loss of SCT in the maternal gut results in undesirable phenotypes developed in offspring including enhanced high-fat diet (HFD)-induced obesity and attenuated browning of inguinal white adipose tissue (iWAT). Mechanistically, loss of maternal SCT represses iWAT browning in offspring by a global change in genome methylation pattern through upregulation of DNMT1. SCT functions to facilitate ubiquitination and degradation of DNMT1 by activating AMPKα, which contributes to the observed alte"],"journal":["EMBO reports"],"pubmed_title":["Maternal secretin ameliorates obesity by promoting white adipose tissue browning in offspring."],"pmcid":["PMC9253765"],"funding_grant_id":["31900841","91957205","32071166","81801541","JUSRP221001"],"pubmed_authors":["Qian H","Liu J","Zhang D","Zhang K","Lu Y","Jiang H","Fan M","Wu D","Zhang L","Ying H","Wang L","Chow BK","Nie C","Li X","Hu C","Li Y","Zhao L","Xue L","Wang Y","Sun J","Wong J"],"additional_accession":[]},"is_claimable":false,"name":"Maternal secretin ameliorates obesity by promoting white adipose tissue browning in offspring.","description":"Our knowledge of the coordination of intergenerational inheritance and offspring metabolic reprogramming by gastrointestinal endocrine factors is largely unknown. Here, we showed that secretin (SCT), a brain-gut peptide, is downregulated by overnutrition in pregnant mice and women. More importantly, genetic loss of SCT in the maternal gut results in undesirable phenotypes developed in offspring including enhanced high-fat diet (HFD)-induced obesity and attenuated browning of inguinal white adipose tissue (iWAT). Mechanistically, loss of maternal SCT represses iWAT browning in offspring by a global change in genome methylation pattern through upregulation of DNMT1. SCT functions to facilitate ubiquitination and degradation of DNMT1 by activating AMPKα, which contributes to the observed alte","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Jul","modification":"2025-04-04T14:40:28.279Z","creation":"2025-04-04T14:40:28.279Z"},"accession":"S-EPMC9253765","cross_references":{"pubmed":["35652247"],"doi":["10.15252/embr.202154132"]}}