DNA–Protein Crosslink Proteolysis Repair

Bruno Vaz, Marta Popovic, Kristijan Ramadan*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

64 Citations (Scopus)

Abstract

Proteins that are covalently bound to DNA constitute a specific type of DNA lesion known as DNA–protein crosslinks (DPCs). DPCs represent physical obstacles to the progression of DNA replication. If not repaired, DPCs cause stalling of DNA replication forks that consequently leads to DNA double-strand breaks, the most cytotoxic DNA lesion. Although DPCs are common DNA lesions, the mechanism of DPC repair was unclear until now. Recent work unveiled that DPC repair is orchestrated by proteolysis performed by two distinct metalloproteases, SPARTAN in metazoans and Wss1 in yeast. This review summarizes recent discoveries on two proteases in DNA replication-coupled DPC repair and establishes DPC proteolysis repair as a separate DNA repair pathway for genome stability and protection from accelerated aging and cancer.

Original languageEnglish
Pages (from-to)483-495
Number of pages13
JournalTrends in Biochemical Sciences
Volume42
Issue number6
DOIs
Publication statusPublished - Jun 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2017 Elsevier Ltd

ASJC Scopus Subject Areas

  • Biochemistry
  • Molecular Biology

Keywords

  • aging
  • cancer
  • DNA replication
  • DNA–protein crosslink
  • DNA–protein crosslink proteolysis repair
  • genome stability
  • SPARTAN (DVC1) protease
  • Wss1 protease

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