Skip to main content
Log in

The roles of poly(ADP-ribose)-metabolizing enzymes in alkylation-induced cell death

  • Research Article
  • Published:
Cellular and Molecular Life Sciences Aims and scope Submit manuscript

Abstract.

Poly(ADP-ribose) (PAR) has been identified as a DNA damage-inducible cell death signal upstream of apoptosis-inducing factor (AIF). PAR causes the translocation of AIF from mitochondria to the nucleus and triggers cell death. In living cells, PAR molecules are subject to dynamic changes pending on internal and external stress factors. Using RNA interference (RNAi), we determined the roles of poly(ADP-ribose) polymerases-1 and -2 (PARP-1, PARP-2) and poly(ADP-ribose) glycohydrolase (PARG), the key enzymes configuring PAR molecules, in cell death induced by an alkylating agent. We found that PARP-1, but not PARP-2 and PARG, contributed to alkylation-induced cell death. Likewise, AIF translocation was only affected by PARP-1. PARP-1 seems to play a major role configuring PAR as a death signal involving AIF translocation regardless of the death pathway involved.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to F. R. Althaus.

Additional information

Received 7 November 2007; received after revision 19 December 2007; accepted 21 December 2007

O. Cohausz, C. Blenn: These two authors contributed equally to this work.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cohausz, O., Blenn, C., Malanga, M. et al. The roles of poly(ADP-ribose)-metabolizing enzymes in alkylation-induced cell death. Cell. Mol. Life Sci. 65, 644–655 (2008). https://doi.org/10.1007/s00018-008-7516-5

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00018-008-7516-5

Keywords.

Navigation