Metabolic regulation of protein N-alpha-acetylation by Bcl-xL promotes cell survival

Cell. 2011 Aug 19;146(4):607-20. doi: 10.1016/j.cell.2011.06.050.

Abstract

Previous experiments suggest a connection between the N-alpha-acetylation of proteins and sensitivity of cells to apoptotic signals. Here, we describe a biochemical assay to detect the acetylation status of proteins and demonstrate that protein N-alpha-acetylation is regulated by the availability of acetyl-CoA. Because the antiapoptotic protein Bcl-xL is known to influence mitochondrial metabolism, we reasoned that Bcl-xL may provide a link between protein N-alpha-acetylation and apoptosis. Indeed, Bcl-xL overexpression leads to a reduction in levels of acetyl-CoA and N-alpha-acetylated proteins in the cell. This effect is independent of Bax and Bak, the known binding partners of Bcl-xL. Increasing cellular levels of acetyl-CoA by addition of acetate or citrate restores protein N-alpha-acetylation in Bcl-xL-expressing cells and confers sensitivity to apoptotic stimuli. We propose that acetyl-CoA serves as a signaling molecule that couples apoptotic sensitivity to metabolism by regulating protein N-alpha-acetylation.

Publication types

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

MeSH terms

  • Acetylation
  • Animals
  • Apoptosis
  • Caspase 2 / metabolism
  • Cell Line
  • Cell Survival*
  • Embryo, Mammalian / cytology
  • Gene Knockout Techniques
  • HeLa Cells
  • Humans
  • Jurkat Cells
  • Mice
  • Protein Processing, Post-Translational
  • Proteins / metabolism*
  • bcl-X Protein / metabolism*

Substances

  • Proteins
  • bcl-X Protein
  • Caspase 2