The mineralocorticoid receptor forms higher order oligomers upon DNA binding.
Gregory FettweisThomas A JohnsonBrian Almeida-PrietoJulián Weller-PérezDiego M PresmanGordon L HagerDiego Alvarez de la RosaPublished in: Protein science : a publication of the Protein Society (2023)
The prevailing model of steroid hormone nuclear receptor function assumes ligand-induced homodimer formation followed by binding to DNA hormone response elements (HREs). This model has been challenged by evidence showing that the glucocorticoid receptor (GR) forms tetramers upon ligand and DNA binding, which then drive receptor-mediated gene transactivation and transrepression. GR and the closely-related mineralocorticoid receptors (MR) interact to transduce corticosteroid hormone signaling, but whether they share the same quaternary arrangement is unknown. Here, we used a fluorescence imaging technique, Number & Brightness, to study oligomerization in a cell system allowing real-time analysis of receptor-DNA interactions. Agonist-bound MR forms tetramers in the nucleoplasm and higher order oligomers upon binding to HREs. Antagonists form intermediate-size quaternary arrangements, suggesting that large oligomers are essential for function. Divergence between MR and GR quaternary structure is driven by different functionality of known and new multimerization interfaces, which does not preclude formation of heteromers. Thus, influencing oligomerization may be important to selectively modulate corticosteroid signaling.
Keyphrases
- dna binding
- fluorescence imaging
- transcription factor
- magnetic resonance
- circulating tumor
- contrast enhanced
- single cell
- magnetic resonance imaging
- cell free
- single molecule
- binding protein
- genome wide
- high glucose
- oxidative stress
- computed tomography
- endothelial cells
- bone marrow
- dna methylation
- circulating tumor cells
- genome wide identification