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Two genetic circuits repress the Caenorhabditis elegans heterochronic gene lin-28 after translation initiation

Dev Biol. 2002 Mar 15;243(2):215-25. doi: 10.1006/dbio.2001.0563.

Abstract

The heterochronic gene lin-28 of the nematode Caenorhabditis elegans controls the relative timing of diverse developmental events during the animal's larval stages. lin-28 is stage-specifically regulated by two genetic circuits: negatively by the 22-nt RNA lin-4 and positively by the heterochronic gene lin-14. Here, we show that lin-28 is repressed during normal development by a mechanism that acts on its mRNA after translation initiation. We provide evidence that lin-14 inhibits a negative regulation that is independent of the lin-4 RNA and involves the gene daf-12, which encodes a nuclear hormone receptor. The lin-4-independent repression does not affect the initiation of translation on the lin-28 mRNA, and like the lin-4-mediated repression, acts through the gene's 3'-untranslated region. In addition, we find that lin-4 is not sufficient to cause repression of lin-28 if the lin-4-independent circuit is inhibited. Therefore, the lin-4-independent circuit likely contributes substantially to the down-regulation of lin-28 that occurs during normal development. The role of lin-4 may be to initiate or potentiate the lin-4-independent circuit. We speculate that a parallel lin-4-independent regulatory mechanism regulates the expression of lin-14.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans / growth & development
  • Caenorhabditis elegans Proteins / biosynthesis
  • Caenorhabditis elegans Proteins / genetics*
  • Caenorhabditis elegans Proteins / physiology*
  • Centrifugation, Density Gradient
  • Cycloheximide / pharmacology
  • Gene Expression Regulation, Developmental / genetics*
  • Helminth Proteins
  • Larva
  • MicroRNAs
  • Models, Genetic
  • Nuclear Proteins*
  • Peptide Chain Elongation, Translational*
  • Peptide Chain Initiation, Translational*
  • Protein Processing, Post-Translational
  • Protein Synthesis Inhibitors / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Messenger / physiology*
  • Receptors, Cytoplasmic and Nuclear / physiology
  • Repressor Proteins / genetics
  • Repressor Proteins / physiology*
  • Ribosomes / metabolism

Substances

  • Caenorhabditis elegans Proteins
  • DAF-12 protein, C elegans
  • Helminth Proteins
  • LIN-14 protein, C elegans
  • LIN-28 protein, C elegans
  • MicroRNAs
  • Nuclear Proteins
  • Protein Synthesis Inhibitors
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Repressor Proteins
  • lin-4 microRNA, C elegans
  • Cycloheximide