DNA-protein crosslink proteases in genome stability

Commun Biol. 2021 Jan 4;4(1):11. doi: 10.1038/s42003-020-01539-3.

Abstract

Proteins covalently attached to DNA, also known as DNA-protein crosslinks (DPCs), are common and bulky DNA lesions that interfere with DNA replication, repair, transcription and recombination. Research in the past several years indicates that cells possess dedicated enzymes, known as DPC proteases, which digest the protein component of a DPC. Interestingly, DPC proteases also play a role in proteolysis beside DPC repair, such as in degrading excess histones during DNA replication or controlling DNA replication checkpoints. Here, we discuss the importance of DPC proteases in DNA replication, genome stability and their direct link to human diseases and cancer therapy.

Publication types

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

MeSH terms

  • Aspartic Acid Proteases / metabolism
  • DNA Damage
  • DNA Replication
  • DNA-Binding Proteins / metabolism*
  • Genomic Instability*
  • Humans
  • Nuclear Proteins / metabolism
  • Protein Processing, Post-Translational
  • Receptors, Virus / metabolism

Substances

  • DNA-Binding Proteins
  • FAM111A protein, human
  • GCNA protein, human
  • Nuclear Proteins
  • Receptors, Virus
  • SPRTN protein, human
  • Aspartic Acid Proteases
  • DDI2 protein, human