Structure-specific DNA endonuclease Mus81/Eme1 generates DNA damage caused by Chk1 inactivation

PLoS One. 2011;6(8):e23517. doi: 10.1371/journal.pone.0023517. Epub 2011 Aug 17.

Abstract

The DNA-damage checkpoint kinase Chk1 is essential in higher eukaryotes due to its role in maintaining genome stability in proliferating cells. CHK1 gene deletion is embryonically lethal, and Chk1 inhibition in replicating cells causes cell-cycle defects that eventually lead to perturbed replication and replication-fork collapse, thus generating endogenous DNA damage. What is the cause of replication-fork collapse when Chk1 is inactivated, however, remains poorly understood. Here, we show that generation of DNA double-strand breaks at replication forks when Chk1 activity is compromised relies on the DNA endonuclease complex Mus81/Eme1. Importantly, we show that Mus81/Eme1-dependent DNA damage--rather than a global increase in replication-fork stalling--is the cause of incomplete replication in Chk1-deficient cells. Consequently, Mus81/Eme1 depletion alleviates the S-phase progression defects associated with Chk1 deficiency, thereby increasing cell survival. Chk1-mediated protection of replication forks from Mus81/Eme1 even under otherwise unchallenged conditions is therefore vital to prevent uncontrolled fork collapse and ensure proper S-phase progression in human cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Checkpoint Kinase 1
  • Comet Assay
  • DNA / chemistry
  • DNA / genetics
  • DNA Breaks, Double-Stranded / drug effects
  • DNA Damage*
  • DNA Repair
  • DNA Replication
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Endodeoxyribonucleases / genetics
  • Endodeoxyribonucleases / metabolism*
  • Endonucleases / genetics
  • Endonucleases / metabolism*
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Nucleic Acid Conformation
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • RNA Interference
  • S Phase
  • Thiophenes / pharmacology
  • Urea / analogs & derivatives
  • Urea / pharmacology

Substances

  • 3-(carbamoylamino)-5-(3-fluorophenyl)-N-(3-piperidyl)thiophene-2-carboxamide
  • DNA-Binding Proteins
  • Enzyme Inhibitors
  • Thiophenes
  • Urea
  • DNA
  • Protein Kinases
  • CHEK1 protein, human
  • Checkpoint Kinase 1
  • Eme1 protein, human
  • Endodeoxyribonucleases
  • Endonucleases
  • MUS81 protein, human