Replisome Dynamics and Their Functional Relevance upon DNA Damage through the PCNA Interactome

Cell Rep. 2018 Dec 26;25(13):3869-3883.e4. doi: 10.1016/j.celrep.2018.11.099.

Abstract

Eukaryotic cells use copious measures to ensure accurate duplication of the genome. Various genotoxic agents pose threats to the ongoing replication fork that, if not efficiently dealt with, can result in replication fork collapse. It is unknown how replication fork is precisely controlled and regulated under different conditions. Here, we examined the complexity of replication fork composition upon DNA damage by using a PCNA-based proteomic screen to uncover known and unexplored players involved in replication and replication stress response. We used camptothecin or UV radiation, which lead to fork-blocking lesions, to establish a comprehensive proteomics map of the replisome under such replication stress conditions. We identified and examined two potential candidate proteins WIZ and SALL1 for their roles in DNA replication and replication stress response. In addition, our unbiased screen uncovered many prospective candidate proteins that help fill the knowledge gap in understanding chromosomal DNA replication and DNA repair.

Keywords: DNA damage; DNA replication; PCNA; proximity labeling; replication stress.

Publication types

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

MeSH terms

  • Camptothecin / pharmacology
  • DNA Damage*
  • DNA Replication / drug effects
  • DNA Replication / radiation effects
  • DNA-Directed DNA Polymerase / metabolism*
  • HEK293 Cells
  • Humans
  • Kruppel-Like Transcription Factors / metabolism
  • Multienzyme Complexes / metabolism*
  • Proliferating Cell Nuclear Antigen / metabolism*
  • Protein Interaction Maps* / drug effects
  • Protein Interaction Maps* / radiation effects
  • Proteome / metabolism
  • S Phase / drug effects
  • S Phase / radiation effects
  • Stress, Physiological / drug effects
  • Stress, Physiological / radiation effects
  • Substrate Specificity / drug effects
  • Substrate Specificity / radiation effects
  • Ultraviolet Rays

Substances

  • Kruppel-Like Transcription Factors
  • Multienzyme Complexes
  • Proliferating Cell Nuclear Antigen
  • Proteome
  • WIZ protein, human
  • DNA synthesome
  • DNA-Directed DNA Polymerase
  • Camptothecin