Resurrecting the ancestral steroid receptor: ancient origin of estrogen signaling

Science. 2003 Sep 19;301(5640):1714-7. doi: 10.1126/science.1086185.

Abstract

Receptors for sex and adrenal steroid hormones are absent from fully sequenced invertebrate genomes and have not been recovered from other invertebrates. Here we report the isolation of an estrogen receptor ortholog from the mollusk Aplysia californica and the reconstruction, synthesis, and experimental characterization of functional domains of the ancestral protein from which all extant steroid receptors (SRs) evolved. Our findings indicate that SRs are extremely ancient and widespread, having diversified from a primordial gene before the origin of bilaterally symmetric animals, and that this ancient receptor had estrogen receptor-like functionality. This gene was lost in the lineage leading to arthropods and nematodes and became independent of hormone regulation in the Aplysia lineage.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Aplysia / chemistry
  • Aplysia / genetics
  • Aplysia / metabolism*
  • Biological Evolution
  • CHO Cells
  • Cloning, Molecular
  • Cricetinae
  • DNA / metabolism
  • Estrogens / metabolism*
  • Estrogens / pharmacology
  • Evolution, Molecular*
  • Gene Duplication
  • Humans
  • Ligands
  • Likelihood Functions
  • Molecular Sequence Data
  • Mutation
  • Phylogeny*
  • Polymerase Chain Reaction
  • Protein Structure, Tertiary
  • Receptors, Estrogen / chemistry
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / isolation & purification
  • Receptors, Estrogen / metabolism*
  • Receptors, Steroid / chemistry
  • Receptors, Steroid / genetics
  • Receptors, Steroid / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction
  • Steroids / metabolism
  • Steroids / pharmacology
  • Transcription, Genetic
  • Transfection

Substances

  • Estrogens
  • Ligands
  • Receptors, Estrogen
  • Receptors, Steroid
  • Recombinant Fusion Proteins
  • Steroids
  • DNA