Development of yeast reporter assay for screening specific ligands of retinoic acid and retinoid X receptor subtypes

作者：Shiizaki Kazuhiro; Yoshikawa Tomoya; Takada Eiji; Hirose Shizuma; Ito Harashima Sayoko; Kawanishi Masanobu; Yagi Takashi^*

来源：Journal of Pharmacological and Toxicological Methods, 2014, 69(3): 245-252.

DOI：10.1016/j.vascn.2014.01.007

• Saccharomyces cerevisiae
• Retinoic acid receptor alpha,beta,gamma
• Retinoid X receptor alpha,beta,gamma
• Reporter assay
• Endocrine disruptors

Introduction: Retinoic acids are essential for embryonic development, tissue organization, and homeostasis and act via retinoic acid receptors (RARs) that form heterodimers with retinoid X receptors (RXRs). Human RARs and RXRs include the three subtypes alpha,beta and gamma, which have varying distributions and physiological functions among human tissues. Recent reports show that subtype-specific binding of several chemicals to RARs or RXRs may lead to endocrine disruption. To evaluate these ligand-like chemicals, convenient assay systems for each receptor subtype are required. Methods: We developed reporter assay yeasts to screen ligands for RXR subtype receptor homodimers. To screen RAR ligands, yeasts were engineered to express RAR subtypes with defective RXRa, which fails to bind to coactivators because of its shortened c-terminus. Results: These assay yeasts were validated using known RXR- and RAR-specific ligands and subtype-specific responses were clearly shown. Subtype- specific ligand activities of the suspected chemical RAR or RXR ligands o-t-butylphenol, triphenyltin chloride, tributyltin chloride, and 4-nonylphenol were determined. Discussion: The present assay yeasts may be valuable tools for subtype-specific assessments of unidentified environmental ligand chemicals and receptor-specific pharmaceuticals.

• 出版日期2014-6