Choi, SungwooKang, Ju-GyeongTran, Yen T. H.Jeong, Sun-HyePark, Kun-YoungShin, HyemiKim, Young HoonPark, MyungsunNahmgoong, HahnSeol, TaejunJeon, HaeyonKim, YeongminPark, SangheeKim, Hee-jooKim, Min-SeobLi, XiaoxuBou Sleiman, MarounLee, EriesChoi, JinhyukEisenbarth, DavidLee, Sang HeonCho, SuhyeonMoore, David D.Auwerx, JohanKim, Il-YoungKim, Jae BumPark, Jong-EunLim, Dae-SikSuh, Jae Myoung2024-06-192024-06-192024-06-192024-05-0110.1038/s42255-024-01045-4https://infoscience.epfl.ch/handle/20.500.14299/208704WOS:001236028300001Adipose tissues serve as an energy reservoir and endocrine organ, yet the mechanisms that coordinate these functions remain elusive. Here, we show that the transcriptional coregulators, YAP and TAZ, uncouple fat mass from leptin levels and regulate adipocyte plasticity to maintain metabolic homeostasis. Activating YAP/TAZ signalling in adipocytes by deletion of the upstream regulators Lats1 and Lats2 results in a profound reduction in fat mass by converting mature adipocytes into delipidated progenitor-like cells, but does not cause lipodystrophy-related metabolic dysfunction, due to a paradoxical increase in circulating leptin levels. Mechanistically, we demonstrate that YAP/TAZ-TEAD signalling upregulates leptin expression by directly binding to an upstream enhancer site of the leptin gene. We further show that YAP/TAZ activity is associated with, and functionally required for, leptin regulation during fasting and refeeding. These results suggest that adipocyte Hippo-YAP/TAZ signalling constitutes a nexus for coordinating adipose tissue lipid storage capacity and systemic energy balance through the regulation of adipocyte plasticity and leptin gene transcription.|The transcriptional coregulators YAP/TAZ are shown to directly control leptin gene transcription, thereby uncoupling adipose tissue mass from leptin levels.Life Sciences & BiomedicineObese GeneInsulin-ResistanceDiabetes-MellitusYap PathwayFood-IntakeMiceGlucoseTissueTazProliferationtext::journal::journal article::research article