Strongyloides stercoralis daf-2 encodes a divergent ortholog of Caenorhabditis elegans DAF-2

Int J Parasitol. 2013 Jun;43(7):515-20. doi: 10.1016/j.ijpara.2013.01.008. Epub 2013 Mar 13.

Abstract

We hypothesise that developmental arrest in infectious larvae of parasitic nematodes is regulated by signalling pathways homologous to Caenorhabditis elegans DAF (dauer formation) pathways. Alignment of Strongyloides stercoralis (Ss) DAF-2 with DAF-2 of C. elegans and homologs of other species shows that most structural motifs in these insulin-like receptors are conserved. However, the catalytic domain of Ss-DAF-2 contains two substitutions (Q1242 and Q1256), that would result in constitutive dauer formation in C. elegans or diabetes in vertebrate animals. Ss-daf-2 also shows two alternately spliced isoforms, the constitutively expressed Ss-daf-2a, and Ss-daf-2b, which is only expressed in stages leading to parasitism.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Substitution
  • Animals
  • Caenorhabditis elegans Proteins / genetics
  • Catalytic Domain
  • Conserved Sequence
  • DNA, Helminth / chemistry
  • DNA, Helminth / genetics
  • Helminth Proteins / genetics*
  • Molecular Sequence Data
  • Protein Isoforms
  • RNA Splicing
  • Receptor, Insulin / genetics*
  • Sequence Alignment
  • Sequence Analysis, DNA
  • Sequence Homology, Amino Acid
  • Strongyloides stercoralis / genetics*

Substances

  • Caenorhabditis elegans Proteins
  • DNA, Helminth
  • Helminth Proteins
  • Protein Isoforms
  • DAF-2 protein, C elegans
  • Receptor, Insulin

Associated data

  • GENBANK/JX171292
  • GENBANK/JX416330
  • GENBANK/KC312931