NR3E receptors in cnidarians : a new family of steroid receptor relatives extends the possible mechanisms for ligand binding
NR3E receptors in cnidarians : a new family of steroid receptor relatives extends the possible mechanisms for ligand binding
Date
2018-06
Authors
Khalturin, Konstantin
Billas, Isabelle M. L.
Chebaro, Yassmine
Reitzel, Adam M.
Tarrant, Ann M.
Laudet, Vincent
Markov, Gabriel V.
Billas, Isabelle M. L.
Chebaro, Yassmine
Reitzel, Adam M.
Tarrant, Ann M.
Laudet, Vincent
Markov, Gabriel V.
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Keywords
A-ring aromatic steroid
Aromatization
Steroid receptor
Cnidarian
Aromatization
Steroid receptor
Cnidarian
Abstract
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.
Description
Author Posting. © The Author(s), 2018. This is the author's version of the work. It is posted here under a nonexclusive, irrevocable, paid-up, worldwide license granted to WHOI. It is made available for personal use, not for redistribution. The definitive version was published in Journal of Steroid Biochemistry and Molecular Biology 184 (2018): 11-19, doi:10.1016/j.jsbmb.2018.06.014.