PUBLICATION

Families of Nuclear Receptors in Vertebrate Models: Characteristic and Comparative Toxicological Perspective

Authors
Zhao, Y., Zhang, K., Giesy, J.P., Hu, J.
ID
ZDB-PUB-150226-13
Date
2015
Source
Scientific Reports   5: 8554 (Journal)
Registered Authors
Keywords
Evolutionary ecology, Environmental sciences
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Evolution, Molecular
  • Genome
  • Humans
  • Models, Animal*
  • Phylogeny
  • Receptors, Cytoplasmic and Nuclear/classification
  • Receptors, Cytoplasmic and Nuclear/genetics*
  • Receptors, Cytoplasmic and Nuclear/metabolism
  • Sequence Alignment
  • Vertebrates/genetics*
PubMed
25711679 Full text @ Sci. Rep.
Abstract
Various synthetic chemicals are ligands for nuclear receptors (NRs) and can cause adverse effects in vertebrates mediated by NRs. While several model vertebrates, such as mouse, chicken, western clawed frog and zebrafish, are widely used in toxicity testing, few NRs have been well described for most of these classes. In this report, NRs in genomes of 12 vertebrates are characterized via bioinformatics approaches. Although numbers of NRs varied among species, with 40-42 genes in birds to 66-74 genes in teleost fishes, all NRs had clear homologs in human and could be categorized into seven subfamilies defined as NR0B-NR6A. Phylogenetic analysis revealed conservative evolutionary relationships for most NRs, which were consistent with traditional morphology-based systematics, except for some exceptions in Dolphin (Tursiops truncatus). Evolution of PXR and CAR exhibited unexpected multiple patterns and the existence of CAR possibly being traced back to ancient lobe-finned fishes and tetrapods (Sarcopterygii). Compared to the more conservative DBD of NRs, sequences of LBD were less conserved: Sequences of THRs, RARs and RXRs were e90% similar to those of the human, ERs, AR, GR, ERRs and PPARs were more variable with similarities of 60%-100% and PXR, CAR, DAX1 and SHP were least conserved among species.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping