The Caenorhabditis elegans gene lin-26 can trigger epithelial differentiation without conferring tissue specificity

Dev Biol. 2001 Jul 15;235(2):410-21. doi: 10.1006/dbio.2001.0294.

Abstract

How epithelial cell fates become specified is poorly understood. We have previously shown that the putative C2H2 zinc-finger transcription factor LIN-26 is required for the differentiation of ectodermal and mesodermal epithelial cells in Caenorhabditis elegans. Here, we report that ectopic LIN-26 expression during early gastrulation transforms most blastomeres into epithelial-like cells. Specifically, LIN-26 induced the expression of three epithelial markers: the adherens junction protein JAM-1; DLG-1, which is essential for the assembly of JAM-1 at junctions; and CHE-14, which is involved in apical trafficking. Furthermore, ultrastructural studies revealed that ectopic LIN-26 expression induced the formation of adherens-like junctions. However, ectopic lin-26 expression did not confer any tissue-specific cell fate, such as the epidermal cell fate, as evidenced from the observation that several epidermal-specific genes were not induced. Conversely, we show that epidermal cells displayed some polarity defects in lin-26 mutants. We conclude that lin-26 can induce epithelial differentiation and that epitheliogenesis is not a default pathway in C. elegans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Blastomeres / metabolism
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans Proteins*
  • Cell Adhesion Molecules*
  • Cell Differentiation
  • Cell Lineage
  • DNA, Complementary / metabolism
  • DNA-Binding Proteins / genetics*
  • Drosophila Proteins*
  • Ectoderm / metabolism
  • Embryo, Nonmammalian / ultrastructure
  • Epidermis / embryology
  • Epidermis / metabolism
  • Gastrula / metabolism
  • Green Fluorescent Proteins
  • Hot Temperature
  • Insect Proteins / metabolism
  • Luminescent Proteins / metabolism
  • Membrane Proteins / metabolism
  • Mesoderm / metabolism
  • Microscopy, Electron
  • Models, Biological
  • Phenotype
  • Receptors, Cell Surface*
  • Temperature
  • Transcription Factors / genetics*
  • Tumor Suppressor Proteins*

Substances

  • AJM-1 protein, C elegans
  • Caenorhabditis elegans Proteins
  • Cell Adhesion Molecules
  • DNA, Complementary
  • DNA-Binding Proteins
  • Drosophila Proteins
  • Insect Proteins
  • Luminescent Proteins
  • Membrane Proteins
  • Receptors, Cell Surface
  • Transcription Factors
  • Tumor Suppressor Proteins
  • lin-26 protein, C elegans
  • dlg1 protein, Drosophila
  • Green Fluorescent Proteins