A single nucleotide in an estrogen-related receptor α site can dictate mode of binding and peroxisome proliferator-activated receptor γ coactivator 1α activation of target promoters

Abstract

The orphan nuclear receptor estrogen-related receptor α (ERRα, NR3B1) is a constitutively active transcription factor that controls multiple processes, most notably mitochondrial function. ERRα preferentially binds to a nine-nucleotide extended half-site sequence TNAAGGTCA, referred to as the ERRE, as either a monomer or a dimer, although how the mode of DNA binding is dictated remains to be determined. Here, we used variants of the extended half-site sequence and selective DNA binding domain mutants of ERRα to investigate the effects of ERRE sequence specificity on ERRα DNA binding mode, transactivation and interaction with the coactivator protein peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α). We found that the base at the N position of the TNAAGGTCA sequence dictated ERRα binding preference as a monomer or dimer. In addition, we demonstrated that the threonine residue at position 124 (Thr124) was a determinant of ERRα DNA-dependent dimerization. Transfection experiments also indicated that substituting a thymidine for a cytosine at the N position in the ERRE of the native ERRα target promoter trefoil factor 1 (TFF1) considerably diminished the transcriptional response of the ERRα/PGC- 1α complex. These results suggest that a single nucleotide in an ERRα binding site can determine specific configuration to the receptor and productive interaction with the coactivator PGC-1α. Copyright © 2006 by The Endocrine Society.