Beclin 1 self-association is independent of autophagy induction by amino acid deprivation and rapamycin treatment

J Cell Biochem. 2010 Aug 1;110(5):1262-71. doi: 10.1002/jcb.22642.

Abstract

Autophagy, a process of self-digestion of cellular constituents, regulates the balance between protein synthesis and protein degradation. Beclin 1 represents an important component of the autophagic machinery. It interacts with proteins that positively regulate autophagy, such as Vps34, UVRAG, and Ambra1, as well as with anti-apoptotic proteins such as Bcl-2 via its BH3-like domain to negatively regulate autophagy. Thus, Beclin 1 interactions with several proteins may regulate autophagy. To identify novel Beclin 1 interacting proteins, we utilized a GST-Beclin 1 fusion protein. Using mass spectroscopic analysis, we identified Beclin 1 as a protein that interacts with GST-Beclin 1. Further examination by cross linking and co-immunoprecipitation experiments confirmed that Beclin 1 self-interacts and that the coiled coil and the N-terminal region of Beclin 1 contribute to its oligomerization. Importantly, overexpression of vps34, UVRAG, or Bcl-x(L), had no effect on Beclin 1 self-interaction. Moreover, this self-interaction was independent of autophagy induction by amino acid deprivation or rapamycin treatment. These results suggest that full-length Beclin 1 is a stable oligomer under various conditions. Such an oligomer may provide a platform for further protein-protein interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism
  • Amino Acids / pharmacology*
  • Animals
  • Antibiotics, Antineoplastic / pharmacology
  • Apoptosis Regulatory Proteins / chemistry
  • Apoptosis Regulatory Proteins / genetics
  • Apoptosis Regulatory Proteins / metabolism*
  • Autophagy / drug effects*
  • Beclin-1
  • Binding Sites / genetics
  • COS Cells
  • Cell Line
  • Cell Line, Tumor
  • Chlorocebus aethiops
  • Glutathione Transferase / genetics
  • Glutathione Transferase / metabolism
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Humans
  • Immunoblotting
  • Immunoprecipitation
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protein Binding
  • Protein Multimerization
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Sirolimus / pharmacology*
  • Transfection
  • Tumor Suppressor Proteins / metabolism
  • bcl-X Protein / metabolism

Substances

  • Amino Acids
  • Antibiotics, Antineoplastic
  • Apoptosis Regulatory Proteins
  • BECN1 protein, human
  • Beclin-1
  • Membrane Proteins
  • Recombinant Fusion Proteins
  • Tumor Suppressor Proteins
  • UVRAG protein, human
  • bcl-X Protein
  • Green Fluorescent Proteins
  • Glutathione Transferase
  • Sirolimus