Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, CNRS UMR5242, Ecole Normale Supérieure de Lyon, 69342 Lyon, France.
Int J Mol Sci. 2023 Feb 21;24(5):4265. doi: 10.3390/ijms24054265.
Estrogen-related receptors (ERRα, β and γ in mammals) are orphan members of the nuclear receptor superfamily acting as transcription factors. ERRs are expressed in several cell types and they display various functions in normal and pathological contexts. Amongst others, they are notably involved in bone homeostasis, energy metabolism and cancer progression. In contrast to other nuclear receptors, the activities of the ERRs are apparently not controlled by a natural ligand but they rely on other means such as the availability of transcriptional co-regulators. Here we focus on ERRα and review the variety of co-regulators that have been identified by various means for this receptor and their reported target genes. ERRα cooperates with distinct co-regulators to control the expression of distinct sets of target genes. This exemplifies the combinatorial specificity of transcriptional regulation that induces discrete cellular phenotypes depending on the selected coregulator. We finally propose an integrated view of the ERRα transcriptional network.
雌激素相关受体(哺乳动物中的 ERRα、β 和 γ)是核受体超家族的孤儿成员,作为转录因子发挥作用。ERRs 在多种细胞类型中表达,并在正常和病理情况下发挥各种功能。它们特别参与骨稳态、能量代谢和癌症进展。与其他核受体不同,ERRs 的活性显然不是由天然配体控制的,而是依赖于其他手段,如转录共调节剂的可用性。在这里,我们重点关注 ERRα,并回顾了通过各种方法为该受体鉴定的各种共调节剂及其报道的靶基因。ERRα 与不同的共调节剂合作,以控制不同靶基因的表达。这说明了转录调控的组合特异性,根据所选共调节剂诱导不同的细胞表型。最后,我们提出了 ERRα 转录网络的综合观点。