Skip to main content
eScholarship
Open Access Publications from the University of California

Evolution of 17beta-Hydroxysteroid Dehydrogenases and Their Role in Androgen, Estrogen and Retinoid Action

  • Author(s): Baker, Michael E
  • et al.
Abstract

17beta-hydroxysteroid dehydrogenases (17beta-HSDs) regulate androgen and estrogen concentrations in mammals. By 1995, four distinct enzymes with 17beta-HSD activity had been identified: 17beta-HSD-types 1 and 3, which in vivo are NADPH-dependent reductases; 17beta-HSD-types 2 and 4, which in vivo are NAD+-dependent oxidases. Since then six additional enzymes with 17beta-HSD activity have been isolated from mammals. With the exception of 17beta-HSD–type 5, which belongs to the aldoketo-reductase (AKR) family, these 17beta-HSDs belong to the short chain dehydrogenases/reductases (SDR) family. Several 17beta-HSDs appear to be examples of convergent evolution. That is, 17beta-HSD activity arose several times from different ancestors. Some 17beta-HSDs share a common ancestor with retinoid oxido-reductases and have retinol dehydrogenase activity. 17beta-HSD-types 2, 6 and 9 appear to have diverged from ancestral retinoid dehydrogenases early in the evolution of deuterostomes during the Cambrian, about 540 million years ago. This coincided with the origin of nuclear receptors for androgens and estrogens suggesting that expression of 17beta-HSDs had an important role in the early evolution of the physiological response to androgens and estrogens.

Many UC-authored scholarly publications are freely available on this site because of the UC Academic Senate's Open Access Policy. Let us know how this access is important for you.

Main Content
Current View