Deleted in cancer 1 (DICE1) is an essential protein controlling the topology of the inner mitochondrial membrane in C. elegans

Development. 2006 Sep;133(18):3597-606. doi: 10.1242/dev.02534. Epub 2006 Aug 16.

Abstract

DICE1 (deleted in cancer 1), first identified in human lung carcinoma cell lines, is a candidate tumor suppressor, but the details of its activity remain largely unknown. We have found that RNA interference of its C. elegans homolog (DIC-1) produced inviable embryos with increased apoptosis, cavities in cells and abnormal morphogenesis. In the dic-1(RNAi) germ line, ced-3-dependent apoptosis increased, and cell cavities appeared at the late-pachytene/oogenic stage, leading to defective oogenesis. Immunofluorescence microscopy of DIC-1 revealed its ubiquitous expression in the form of cytoplasmic foci, and cryoelectron microscopy narrowed down the location of the foci to the inner membrane of mitochondria. After dic-1 RNAi, mitochondria had an irregular morphology and contained numerous internal vesicles. Homozygous embryos from a heterozygous dic-1 mother arrested at the L3 larval stage, in agreement with the essential role of DIC-1 in mitochondria. In summary, C. elegans DIC-1 plays a crucial role in the formation of normal morphology of the mitochondrial cristae/inner membrane. Our results suggest that human DICE1 may have several functions in multiple intracellular locations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Apoptosis / physiology
  • Caenorhabditis elegans / embryology
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans / ultrastructure
  • Caenorhabditis elegans Proteins / genetics*
  • Caenorhabditis elegans Proteins / metabolism
  • Caenorhabditis elegans Proteins / physiology
  • Caspases / genetics
  • Caspases / metabolism
  • Cells, Cultured
  • Cryoelectron Microscopy / methods
  • Genetic Complementation Test
  • Germ Cells / cytology
  • Germ Cells / metabolism
  • Germ Cells / ultrastructure
  • Gonads / cytology
  • Gonads / metabolism
  • Gonads / ultrastructure
  • Green Fluorescent Proteins / analysis
  • Green Fluorescent Proteins / genetics
  • Humans
  • Immunohistochemistry
  • Microscopy, Fluorescence
  • Mitochondrial Membranes / metabolism*
  • Mitochondrial Membranes / physiology
  • Mitochondrial Membranes / ultrastructure
  • Models, Genetic
  • Morphogenesis / genetics
  • Morphogenesis / physiology
  • Mutation / genetics
  • Oogenesis / genetics
  • Oogenesis / physiology
  • RNA Interference / physiology
  • Recombinant Fusion Proteins / analysis
  • Recombinant Fusion Proteins / genetics
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism
  • Tumor Suppressor Proteins / physiology

Substances

  • Caenorhabditis elegans Proteins
  • Recombinant Fusion Proteins
  • Tumor Suppressor Proteins
  • Green Fluorescent Proteins
  • Caspases
  • ced-3 protein, C elegans