Alteration of the stability of Bag-1 protein in the control of olfactory neuronal apoptosis

J Cell Sci. 2001 Apr;114(Pt 7):1409-16. doi: 10.1242/jcs.114.7.1409.

Abstract

Normal apoptosis occurs continuously in the olfactory neuroepithelium of adult vertebrates, making it a useful model for studying neuronal apoptosis. Here we demonstrate that overexpression of the anti-apoptotic Bag-1 gene in olfactory neuronal cells confers a strong resistance to apoptosis. Conversely decreased levels of Bag-1 were found to precede a massive wave of olfactory neuronal apoptosis triggered by synaptic target ablation. We show that the decrease is brought about by ubiquitination and subsequent degradation of the Bag-1 protein. The ring finger protein Siah-2 is a likely candidate for the ubiquitination reaction since Siah-2 mRNA accumulated in lesioned olfactory neuroepithelium and overexpression of Siah-2 stimulated Bag-1 ubiquitination and degradation in transient expression assays. These results together identify destabilization of Bag-1 as a necessary step in olfactory neuronal apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis*
  • COS Cells
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Chlorocebus aethiops
  • DNA-Binding Proteins
  • Dopamine / pharmacology
  • Down-Regulation
  • Gene Expression
  • Mice
  • Molecular Sequence Data
  • Neurons / cytology*
  • Neurons / drug effects
  • Nuclear Proteins / metabolism
  • Olfactory Mucosa / cytology*
  • Transcription Factors
  • Ubiquitin-Protein Ligases
  • Ubiquitins / genetics
  • Up-Regulation

Substances

  • BCL2-associated athanogene 1 protein
  • Carrier Proteins
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Transcription Factors
  • Ubiquitins
  • Ubiquitin-Protein Ligases
  • seven in absentia proteins
  • Dopamine