Molecular Zoology Team, Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, Université Lyon 1, CNRS, Institut National de la Recherche Agronomique (INRA), École Normale Supérieure de Lyon, 46 allée d'Italie, 69364 Lyon Cedex 07, France.
Evolution des Régulations Endocriniennes, Département Régulations, Développement et Diversité Moléculaire, CNRS UMR 7221, Sorbonne Universités, Muséum National d'Histoire Naturelle (MNHN), Paris, France.
Sci Adv. 2017 Mar 31;3(3):e1601778. doi: 10.1126/sciadv.1601778. eCollection 2017 Mar.
The origin of ancient ligand/receptor couples is often analyzed via reconstruction of ancient receptors and, when ligands are products of metabolic pathways, they are not supposed to evolve. However, because metabolic pathways are inherited by descent with modification, their structure can be compared using cladistic analysis. Using this approach, we studied the evolution of steroid hormones. We show that side-chain cleavage is common to most vertebrate steroids, whereas aromatization was co-opted for estrogen synthesis from a more ancient pathway. The ancestral products of aromatic activity were aromatized steroids with a side chain, which we named "paraestrols." We synthesized paraestrol A and show that it effectively binds and activates the ancestral steroid receptor. Our study opens the way to comparative studies of biologically active small molecules.
古代配体/受体对的起源通常通过对古代受体的重建来分析,而当配体是代谢途径的产物时,它们不应该进化。然而,由于代谢途径是通过遗传和修饰而继承的,因此可以使用分支分析来比较它们的结构。使用这种方法,我们研究了类固醇激素的进化。我们表明,侧链裂解是大多数脊椎动物类固醇的共同特征,而芳香化作用则是从更古老的途径中共同用于雌激素合成的。芳香化作用的祖先产物是带有侧链的芳香类固醇,我们称之为“paraestrols”。我们合成了 paraestrol A,并表明它可以有效地结合和激活祖先的类固醇受体。我们的研究为生物活性小分子的比较研究开辟了道路。