The DFF40/CAD endonuclease and its role in apoptosis

Acta Biochim Pol. 2000;47(4):1037-44.

Abstract

The sequential generation of large-scale DNA fragments followed by internucleosomal chromatin fragmentation is a biochemical hallmark of apoptosis. One of the nucleases primarily responsible for genomic DNA fragmentation during apoptosis is called DNA Fragmentation Factor 40 (DFF40) or Caspase-activated DNase (CAD). DFF40/CAD is a magnesium-dependent endonuclease specific for double stranded DNA that generates double strand breaks with 3'-hydroxyl ends. DFF40/CAD is activated by caspase-3 that cuts the nuclease's inhibitor DFF45/ICAD. The nuclease preferentially attacks chromatin in the internucleosomal linker DNA. However, the nuclease hypersensitive sites can be detected and DFF40/CAD is potentially involved in large-scale DNA fragmentation as well. DFF40/CAD-mediated DNA fragmentation triggers chromatin condensation that is another hallmark of apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins
  • Apoptosis*
  • Chromatin / metabolism
  • DNA Fragmentation
  • Deoxyribonucleases / metabolism*
  • Deoxyribonucleases / physiology*
  • Dimerization
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Models, Biological
  • Poly-ADP-Ribose Binding Proteins
  • Protein Binding
  • Structure-Activity Relationship

Substances

  • Apoptosis Regulatory Proteins
  • Chromatin
  • Intracellular Signaling Peptides and Proteins
  • Poly-ADP-Ribose Binding Proteins
  • caspase-activated DNase inhibitor
  • DFFB protein, human
  • Deoxyribonucleases