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PMID: 11884032 Published · ppublish English Journal Article

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

Developmental biology ·Vol. 243 ·No. 2 ·2002-03-15 ·Pages 215-25

Seggerson K, Tang L, Moss EG

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,growth & development Caenorhabditis elegans Proteins/biosynthesis,genetics,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,metabolism,physiology Receptors, Cytoplasmic and Nuclear/physiology Repressor Proteins/genetics,physiology Ribosomes/metabolism
Chemicals
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
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Seggerson Kathy
Fox Chase Cancer Center, 7701 Burholme Avenue, Philadelphia, PA 19111, USA.
Tang Lingjuan
Moss Eric G
Article Info
Journal
Developmental biology
Abbr.
Dev Biol
ISSN
0012-1606
Published
2002-03-15
Pages
215-25
Language
English
Region
United States
NLM ID
0372762
Subset
IM
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