Makorin ortholog LEP-2 regulates LIN-28 stability to promote the juvenile-to-adult transition in Caenorhabditis elegans

Development. 2016 Mar 1;143(5):799-809. doi: 10.1242/dev.132738. Epub 2016 Jan 25.

Abstract

The heterochronic genes lin-28, let-7 and lin-41 regulate fundamental developmental transitions in animals, such as stemness versus differentiation and juvenile versus adult states. We identify a new heterochronic gene, lep-2, in Caenorhabditis elegans. Mutations in lep-2 cause a delay in the juvenile-to-adult transition, with adult males retaining pointed, juvenile tail tips, and displaying defective sexual behaviors. In both sexes, lep-2 mutants fail to cease molting or produce an adult cuticle. We find that LEP-2 post-translationally regulates LIN-28 by promoting LIN-28 protein degradation. lep-2 encodes the sole C. elegans ortholog of the Makorin (Mkrn) family of proteins. Like lin-28 and other heterochronic pathway members, vertebrate Mkrns are involved in developmental switches, including the timing of pubertal onset in humans. Based on shared roles, conservation and the interaction between lep-2 and lin-28 shown here, we propose that Mkrns, together with other heterochronic genes, constitute an evolutionarily ancient conserved module regulating switches in development.

Keywords: Developmental timing; Heterochronic pathway; LIN-28/let-7 axis; Mkrn.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Animals
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / physiology*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / physiology*
  • Cell Differentiation
  • Chromosome Mapping
  • Comparative Genomic Hybridization
  • Epistasis, Genetic
  • Female
  • Gene Expression Regulation, Developmental*
  • Genetic Complementation Test
  • Male
  • Molecular Sequence Data
  • Mutagenesis
  • Mutation
  • Phenotype
  • RNA Interference
  • RNA Processing, Post-Transcriptional
  • Repressor Proteins / physiology*
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / physiology*
  • Transgenes

Substances

  • Caenorhabditis elegans Proteins
  • LEP-2 protein, C elegans
  • LIN-28 protein, C elegans
  • Repressor Proteins
  • Ribonucleoproteins