Lack of GPR180 ameliorates hepatic lipid depot via downregulation of mTORC1 signaling.
Ontology highlight
ABSTRACT: Our previous genome-wide association study to explore genetic loci associated with lean nonalcoholic fatty liver disease (NAFLD) in Japan suggested four candidate loci, which were mapped to chr6, chr7, chr12 and chr13. The present study aimed to identify the locus involved functionally in NAFLD around the association signal observed in chr13. Chromosome conformation capture assay and a database survey suggested the intermolecular interaction among DNA fragments in association signals with the adjacent four coding gene promoters. The four genes were further screened by knockdown (KD) in mice using shRNA delivered by an adeno-associated virus vector (AAV8), and KD of G protein-coupled receptor 180 (Gpr180) showed amelioration of hepatic lipid storage. Gpr180 knockout (KO) mice also showed am
SUBMITTER: Yoshida K
PROVIDER: S-EPMC9892563 | biostudies-literature | 2023 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA