ROP-1, an RNA quality-control pathway component, affects Caenorhabditis elegans dauer formation

Proc Natl Acad Sci U S A. 2000 Nov 21;97(24):13233-8. doi: 10.1073/pnas.230284297.

Abstract

Caenorhabditis elegans dauer formation is an alternative larval developmental pathway that the worm can take when environmental conditions become detrimental. Animals can survive several months in this stress-resistant stage and can resume normal development when growth conditions improve. Although the worms integrate a variety of sensory information to commit to dauer formation, it is currently unknown whether they also monitor internal cellular damage. The Ro ribonucleoprotein complex, which was initially described as a human autoantigen, is composed of one major 60-kDa protein, Ro60, that binds to one of four small RNA molecules, designated Y RNAs. Ro60 has been shown to bind mutant 5S rRNA molecules in Xenopus oocytes, suggesting a role for Ro60 in 5S rRNA biogenesis. Analysis of ribosomes from a C. elegans rop-1(-) strain, which is null for the expression of Ro60, demonstrated that they contain a high percentage of mutant 5S rRNA molecules, thereby strengthening the notion of a link between the rop-1 gene product and 5S rRNA quality control. The Ro particle was recently shown to be involved in the resistance of Deinococcus radiodurans to UV irradiation, suggesting a role for the Ro complex in stress resistance. We have studied the role of rop-1 in dauer formation. We present genetic and biochemical evidence that rop-1 interacts with dauer-formation genes and is involved in the regulation of the worms' entry into the dauer stage. Furthermore, we find that the rop-1 gene product undergoes a proteolytic processing step that is regulated by the dauer formation pathway via an aspartic proteinase. These results suggest that the Ro particle may function in an RNA quality-control checkpoint for dauer formation.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans / embryology
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans / growth & development*
  • Caenorhabditis elegans Proteins*
  • Embryo, Nonmammalian / physiology
  • Gene Expression Regulation, Developmental*
  • Genotype
  • Helminth Proteins / genetics*
  • Helminth Proteins / metabolism*
  • Larva
  • Protozoan Proteins / genetics*
  • Protozoan Proteins / metabolism*
  • RNA, Helminth / genetics*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism
  • Receptor, Insulin / metabolism
  • Transforming Growth Factor beta / metabolism

Substances

  • Caenorhabditis elegans Proteins
  • DAF-7 protein, C elegans
  • Helminth Proteins
  • Protozoan Proteins
  • RNA, Helminth
  • RNA-Binding Proteins
  • Transforming Growth Factor beta
  • rhoptry associated protein, Plasmodium
  • DAF-2 protein, C elegans
  • Receptor, Insulin