The RNA-binding protein HuR is a negative regulator in adipogenesis

The RNA-binding protein HuR is a negative regulator in adipogenesis
Title:
The RNA-binding protein HuR is a negative regulator in adipogenesis
Other Titles:
Nature Communications
Keywords:
Publication Date:
10 January 2020
Citation:
Siang, D.T.C., Lim, Y.C., Kyaw, A.M.M. et al. The RNA-binding protein HuR is a negative regulator in adipogenesis. Nat Commun 11, 213 (2020). https://doi.org/10.1038/s41467-019-14001-8
Abstract:
Human antigen R (HuR) is an essential regulator of RNA metabolism, but its function in metabolism remains unclear. This study identifies HuR as a major repressor during adipogenesis. Knockdown and overexpression of HuR in primary adipocyte culture enhances and inhibits adipogenesis in vitro, respectively. Fat-specific knockout of HuR significantly enhances adipogenic gene program in adipose tissues, accompanied by a systemic glucose intolerance and insulin resistance. HuR knockout also results in depot-specific phenotypes: it can repress myogenesis program in brown fat, enhance inflammation program in epidydimal white fat and induce browning program in inguinal white fat. Mechanistically, HuR may inhibit adipogenesis by recognizing and modulating the stability of hundreds of adipocyte transcripts including Insig1, a negative regulator during adipogenesis. Taken together, our work establishes HuR as an important posttranscriptional regulator of adipogenesis and provides insights into how RNA processing contributes to adipocyte development.
License type:
http://creativecommons.org/licenses/by/4.0/
Funding Info:
This work was supported by Singapore National Medical Research Council’s Open Fund - Young Individual Research Grant (OFYIRG) (NMRC/OFYIRG/0080/2018), Open Fund-Individual Research (OF-IRG) Grant (NMRC/OFIRG/0062/2017), Ministry of Education (MOE) Tier2 grant (MOE2017-T2-2-015), National Medical Research Council’s Cooperative Basic Research Grant (CBRG; NMRC/CBRG/0070/2014 and NMRC/CBRG/0101/2016) and Tanoto Initiative in Diabetes Research to L.S.
Description:
ISSN:
2041-1723
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