The Nuclear Receptor HIZR-1 Uses Zinc as a Ligand to Mediate Homeostasis in Response to High Zinc

PLoS Biol. 2017 Jan 17;15(1):e2000094. doi: 10.1371/journal.pbio.2000094. eCollection 2017 Jan.

Abstract

Nuclear receptors were originally defined as endocrine sensors in humans, leading to the identification of the nuclear receptor superfamily. Despite intensive efforts, most nuclear receptors have no known ligand, suggesting new ligand classes remain to be discovered. Furthermore, nuclear receptors are encoded in the genomes of primitive organisms that lack endocrine signaling, suggesting the primordial function may have been environmental sensing. Here we describe a novel Caenorhabditis elegans nuclear receptor, HIZR-1, that is a high zinc sensor in an animal and the master regulator of high zinc homeostasis. The essential micronutrient zinc acts as a HIZR-1 ligand, and activated HIZR-1 increases transcription of genes that promote zinc efflux and storage. The results identify zinc as the first inorganic molecule to function as a physiological ligand for a nuclear receptor and direct environmental sensing as a novel function of nuclear receptors.

MeSH terms

  • Animals
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins / chemistry
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Cation Transport Proteins / genetics
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • DNA / metabolism
  • Enhancer Elements, Genetic / genetics
  • Feedback, Physiological / drug effects
  • Genetic Testing
  • Homeostasis / drug effects*
  • Intestinal Mucosa / metabolism
  • Intestines / drug effects
  • Ligands
  • Mutation / genetics
  • Promoter Regions, Genetic / genetics
  • Protein Domains
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Cytoplasmic and Nuclear / chemistry
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Transcription, Genetic / drug effects
  • Zinc / pharmacology*

Substances

  • CDF-2 protein, C elegans
  • Caenorhabditis elegans Proteins
  • Cation Transport Proteins
  • Ligands
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • DNA
  • Zinc