{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Xu X"],"funding":["National Natural Science Foundation of China","National Natural Science Foundation of China (National Science Foundation of China)"],"pagination":["54-71"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8724286"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["32(1)"],"pubmed_abstract":["The AMP-activated protein kinase (AMPK) is a central regulator of energy homeostasis. Although much has been learned on how low energy status and glucose starvation activate AMPK, how AMPK activity is properly controlled in vivo is still poorly understood. Here we report that UHRF1, an epigenetic regulator highly expressed in proliferating and cancer cells, interacts with AMPK and serves to suppress AMPK activity under both basal and stressed conditions. As a nuclear protein, UHRF1 promotes AMPK nuclear retention and strongly suppresses nuclear AMPK activity toward substrates H2B and EZH2. Importantly, we demonstrate that UHRF1 also robustly inhibits AMPK activity in the cytoplasm compartment, most likely as a consequence of AMPK nucleocytoplasmic shuttling. Mechanistically, we found that "],"journal":["Cell research"],"pubmed_title":["Nuclear UHRF1 is a gate-keeper of cellular AMPK activity and function."],"pmcid":["PMC8724286"],"funding_grant_id":["31730048"],"pubmed_authors":["Ding G","Li J","Ma X","Wei W","Lin SH","Liu W","Zhang CS","Liao L","Ding Y","Huang Y","Chen Z","Lin SC","Zhang Y","Huang X","Lu S","Liu C","Chen X","Xu X","Wong J"],"additional_accession":[]},"is_claimable":false,"name":"Nuclear UHRF1 is a gate-keeper of cellular AMPK activity and function.","description":"The AMP-activated protein kinase (AMPK) is a central regulator of energy homeostasis. Although much has been learned on how low energy status and glucose starvation activate AMPK, how AMPK activity is properly controlled in vivo is still poorly understood. Here we report that UHRF1, an epigenetic regulator highly expressed in proliferating and cancer cells, interacts with AMPK and serves to suppress AMPK activity under both basal and stressed conditions. As a nuclear protein, UHRF1 promotes AMPK nuclear retention and strongly suppresses nuclear AMPK activity toward substrates H2B and EZH2. Importantly, we demonstrate that UHRF1 also robustly inhibits AMPK activity in the cytoplasm compartment, most likely as a consequence of AMPK nucleocytoplasmic shuttling. Mechanistically, we found that ","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Jan","modification":"2025-04-21T15:23:57.074Z","creation":"2025-04-21T15:23:57.074Z"},"accession":"S-EPMC8724286","cross_references":{"pubmed":["34561619"],"doi":["10.1038/s41422-021-00565-y"]}}