Residue correlation networks in nuclear receptors reflect functional specialization and the formation of the nematode-specific P-box

BMC Genomics. 2013;14 Suppl 6(Suppl 6):S1. doi: 10.1186/1471-2164-14-S6-S1. Epub 2013 Oct 25.

Abstract

Background: Nuclear receptors (NRs) are transcription factors which bind small hormones, whose evolutionary history and the presence of different functional surfaces makes them an interesting target for a correlation based analysis.

Results: Correlation analysis of ligand binding domains shows that correlated residue subsets arise from the differences between functional sites in different nuclear receptor subfamilies. For the DNA binding domain, particularly, the analysis shows that the main source of correlation comes from residues that regulate hormone response element specificity, and one of the conserved residue sub-sets arises due to the presence of an unusual sequence for the DNA binding motif known as P-box in nematodes, suggesting the existence of different DBD-DNA specificities in nuclear receptors.

Conclusions: We conclude that DNA specificity and functional surface specialization has independently driven nuclear receptor evolution, and suggest possible binding modes for the class of divergent nuclear receptors in nematodes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Substitution
  • Amino Acids / metabolism*
  • Animals
  • DNA / metabolism
  • DNA-Binding Proteins / metabolism
  • Helminth Proteins / chemistry*
  • Helminth Proteins / metabolism*
  • Ligands
  • Models, Molecular
  • Nematoda / genetics
  • Nematoda / metabolism*
  • Protein Binding
  • Protein Interaction Maps
  • Protein Structure, Tertiary
  • Receptors, Cytoplasmic and Nuclear / chemistry*
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Species Specificity

Substances

  • Amino Acids
  • DNA-Binding Proteins
  • Helminth Proteins
  • Ligands
  • Receptors, Cytoplasmic and Nuclear
  • DNA