WDR76 mediates obesity and hepatic steatosis via HRas destabilization

Jong Chan Park, Woo Jeong Jeong, Seol Hwa Seo, Kang Yell Choi

Research output: Contribution to journalArticlepeer-review

Abstract

Ras/MAPK (mitogen active protein kinase) signaling plays contradictory roles in adipocyte differentiation and is tightly regulated during adipogenesis. However, mechanisms regulating adipocyte differentiation involving Ras protein stability regulation are unknown. Here, we show that WD40 repeat protein 76 (WDR76), a novel Ras regulating E3 linker protein, controls 3T3-L1 adipocyte differentiation through HRas stability regulation. The roles of WDR76 in obesity and metabolic regulation were characterized using a high-fat diet (HFD)-induced obesity model using Wdr76−/− mice and liver-specific Wdr76 transgenic mice (Wdr76Li−TG). Wdr76−/− mice are resistant to HFD-induced obesity, insulin resistance and hyperlipidemia with an increment of HRas levels. In contrast, Wdr76Li-TG mice showed increased HFD-induced obesity, insulin resistance with reduced HRas levels. Our findings suggest that WDR76 controls HFD-induced obesity and hepatic steatosis via HRas destabilization. These data provide insights into the links between WDR76, HRas, and obesity.

Original languageEnglish
Article number19676
JournalScientific reports
Volume9
Issue number1
DOIs
Publication statusPublished - 2019 Dec 1

Bibliographical note

Funding Information:
This work was supported by the National Research Foundation of Korea (NRF) grants funded by the Korean Ministry of Science, ICT, and Future Planning (MSIP); 2015R1A2A1A05001873 and A Mid-Career Researcher Program National Research Lab (2019R1A2C3002751). J.C.P was supported by a postdoctoral fellowship from the NRF (NRF-2017R1A6A3A01012866).

Publisher Copyright:
© 2019, The Author(s).

All Science Journal Classification (ASJC) codes

  • General

Fingerprint Dive into the research topics of 'WDR76 mediates obesity and hepatic steatosis via HRas destabilization'. Together they form a unique fingerprint.

Cite this