| Literature DB >> 25962847 |
Peng Cheng1, Gang Li1, Sheng Sheng Yang2, Rui Liu1, Gang Jin3, Xu Yu Zhou4, Xian Gui Hu1.
Abstract
Menin, encoded by the MEN1 gene, was initially identified as a tumor suppressor for endocrine neoplasia. Our previous report showed that Menin enhances PPARα transactivity preventing triglyceride accumulation in the liver. Here, we further explore the role of Menin in liver steatosis. Transient transfection assays demonstrate that Menin inhibits the transcriptional activity of nuclear receptor liver X receptor α (LXRα). Accordingly, Menin overexpression results in reduced expression of LXRα target genes, such as lipogenic enzymes including SREBP-1c, FASN and SCD-1. Co-immunoprecipitation assays revealed physical interaction between Menin and LXRα. Collectively, our data suggest that Menin acts as a novel corepressor of LXRα and functions as a negative regulator of hepatic lipogenesis.Entities:
Keywords: Hepatic lipogenesis; Liver X receptor α; Menin
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Year: 2015 PMID: 25962847 DOI: 10.1016/j.febslet.2015.04.049
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124