Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10767383 | Biochemical and Biophysical Research Communications | 2007 | 6 Pages |
Abstract
Estrogen-related receptor α (ERRα) is an important mediator of mitochondrial biogenesis and function. To investigate the transcriptional network controlling these phenomena, we investigated mitochondrial gene expression in embryonic fibroblasts isolated from ERRα null mice. Peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) stimulated mitochondrial gene expression program in control cells, but not in the ERRα null cells. Interestingly, the induction of levels of mitochondrial oxidative stress protection genes in response to increased PGC-1α levels was dependent on ERRα. Furthermore, we found that the PGC-1α-mediated induction of estrogen-related receptor γ and nuclear respiratory factor 2 (NRF-2), was dependent on the presence of ERRα. Basal levels of NRF-2 were decreased in the absence of ERRα. The absence of ERRα resulted in a decrease in citrate synthase enzyme activity in response to PGC-1α overexpression. Our results indicate an essential role for ERRα as a key regulator of oxidative metabolism.
Keywords
PGC-1peroxisome proliferator-activated receptor γ coactivator-1αTXN2UCP-3UQCRBNRF-2b2mSOD2ERRMEFsOXPHOSPPARROSMitochondrial gene expressionThioredoxin 2Type 2 diabetesSuperoxide dismutase 2nuclear respiratory factor 2Oxidative phosphorylationOxidative metabolismmouse embryonic fibroblastswildtypeperoxiredoxin 3Peroxiredoxin 5Uncoupling protein 3Reactive oxygen speciesperoxisome proliferator-activated receptorestrogen-related receptor
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Biochemistry
Authors
Shamina M. Rangwala, Xiaoyan Li, Loren Lindsley, Xiaomei Wang, Stacey Shaughnessy, Thomas G. Daniels, Joseph Szustakowski, N.R. Nirmala, Zhidan Wu, Susan C. Stevenson,