Marine Genomics Unit, Okinawa Institute of Science and Technology, 1919-1 Tancha, Onna-son, Kunigami-gun, Okinawa 904-0495, Japan.
Centre for Integrative Biology (CBI), Department of Integrated Structural Biology, IGBMC (Institute of Genetics and of Molecular and Cellular Biology), Illkirch, France; Centre National de la Recherche Scientifique (CNRS) UMR 7104, Illkirch, France; Institut National de la Santé et de la Recherche Médicale (INSERM) U964, Illkirch, France; Université de Strasbourg, Strasbourg, France.
J Steroid Biochem Mol Biol. 2018 Nov;184:11-19. doi: 10.1016/j.jsbmb.2018.06.014. Epub 2018 Jun 22.
Steroid hormone receptors are important regulators of development and physiology in bilaterian animals, but the role of steroid signaling in cnidarians has been contentious. Cnidarians produce steroids, including A-ring aromatic steroids with a side-chain, but these are probably made through pathways different than the one used by vertebrates to make their A-ring aromatic steroids. Here we present comparative genomic analyses indicating the presence of a previously undescribed nuclear receptor family within medusozoan cnidarians, that we propose to call NR3E. This family predates the diversification of ERR/ER/SR in bilaterians, indicating that the first NR3 evolved in the common ancestor of the placozoan and cnidarian-bilaterian with lineage-specific loss in the anthozoans, even though multiple species in this lineage have been shown to produce aromatic steroids, whose function remain unclear. We discovered serendipitously that a cytoplasmic factor within epidermal cells of transgenic Hydra vulgaris can trigger the nuclear translocation of heterologously expressed human ERα. This led us to hypothesize that aromatic steroids may also be present in the medusozoan cnidarian lineage, which includes Hydra, and may explain the translocation of human ERα. Docking experiments with paraestrol A, a cnidarian A-ring aromatic steroid, into the ligand-binding pocket of Hydra NR3E indicates that, if an aromatic steroid is indeed the true ligand, which remains to be demonstrated, it would bind to the pocket through a partially distinct mechanism from the manner in which estradiol binds to vertebrate ER.
甾体激素受体是两侧对称动物发育和生理的重要调节剂,但甾体信号在刺胞动物中的作用一直存在争议。刺胞动物产生甾体,包括带有侧链的 A 环芳甾类,但这些甾体可能是通过不同于脊椎动物用于合成其 A 环芳甾类的途径产生的。在这里,我们进行了比较基因组分析,表明在水母样刺胞动物中存在一个以前未描述的核受体家族,我们提议将其命名为 NR3E。这个家族早于脊椎动物中 ERR/ER/SR 的多样化,表明第一个 NR3 进化在扁形动物和刺胞动物-两侧对称动物的共同祖先中,尽管这个谱系中的多个物种已被证明能产生芳甾类,但它们的功能仍不清楚。我们偶然发现,转基因水螅属表皮细胞中的一种细胞质因子可以触发异源表达的人 ERα 的核转位。这使我们假设芳甾类也可能存在于包括水螅在内的水母样刺胞动物谱系中,这可以解释人 ERα 的转位。将 paraestrol A(一种刺胞动物 A 环芳甾类)与水螅 NR3E 的配体结合口袋对接的实验表明,如果芳香甾体确实是真正的配体(这仍有待证明),它将通过与雌二醇结合脊椎动物 ER 的方式不同的部分机制结合到口袋中。