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| Content Provider | PubMed Central |
|---|---|
| Author | Thiagarajan, Devi Radha, Ananthakrishnan Zhang, Jinghua O’shea, Karen M. Quadri, Nosirudeen Li, Qing Sas, Kelli Jing, Xiao Rosario, Rosa Pennathur, Subramaniam Schmidt, Ann Marie Ramasamy, Ravichandran |
| Abstract | Histone deacetylase 3 (HDAC3), a chromatin modifying enzyme, requires association with the deacetylase containing domain (DAD) of the nuclear receptor co-repressors NCOR1 and SMRT for its stability and activity. Here we show that aldose reductase (AR), the rate-limiting enzyme of the polyol pathway, competes with HDAC3 to bind the NCOR1/SMRT DAD. Increased AR expression leads to HDAC3 degradation followed by increased PPARγ signaling resulting in lipid accumulation in the heart. AR also downregulates expression of nuclear corepressor complex cofactors including Gps2 and Tblr1, thus affecting activity of the nuclear corepressor complex itself. Though AR reduces HDAC3-corepressor complex formation, it specifically de-represses the retinoic acid receptor (RAR), but not other nuclear receptors such as the thyroid receptor (TR) and liver X receptor (LXR). In summary, this work defines a distinct role for AR in lipid and retinoid metabolism through HDAC3 regulation and consequent de-repression of PPARγ and RAR. |
| Related Links | http://dx.doi.org/10.1016/j.celrep.2016.02.086 |
| Ending Page | 196 |
| Page Count | 16 |
| Starting Page | 181 |
| File Format | |
| ISSN | 22111247 |
| e-ISSN | 22111247 |
| Journal | Cell reports |
| Issue Number | 1 |
| Volume Number | 15 |
| Language | English |
| Publisher Date | 2016-04-01 |
| Access Restriction | Open |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Biochemistry, Genetics and Molecular Biology |
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