The ATR-Activation Domain of TopBP1 Is Required for the Suppression of Origin Firing during the S Phase

Int J Mol Sci. 2018 Aug 13;19(8):2376. doi: 10.3390/ijms19082376.

Abstract

The mammalian DNA replication program is controlled at two phases, the licensing of potential origins of DNA replication in early gap 1 (G1), and the selective firing of a subset of licenced origins in the synthesis (S) phase. Upon entry into the S phase, serine/threonine-protein kinase ATR (ATR) is required for successful completion of the DNA replication program by limiting unnecessary dormant origin activation. Equally important is its activator, DNA topoisomerase 2-binding protein 1 (TopBP1), which is also required for the initiation of DNA replication after a rise in S-phase kinase levels. However, it is unknown how the ATR activation domain of TopBP1 affects DNA replication dynamics. Using human cells conditionally expressing a TopBP1 mutant deficient for ATR activation, we show that functional TopBP1 is required in suppressing local dormant origin activation. Our results demonstrate a regulatory role for TopBP1 in the local balancing of replication fork firing within the S phase.

Keywords: ATR; DNA fiber assay; DNA replication; S phase; TopBP1; origin firing.

MeSH terms

  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Line, Tumor
  • DNA, Single-Stranded / metabolism
  • DNA-Binding Proteins / chemistry
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Doxycycline / pharmacology
  • Humans
  • Microscopy, Fluorescence
  • Mutagenesis, Site-Directed
  • Nuclear Proteins / chemistry
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Protein Domains / genetics
  • S Phase
  • Transcription, Genetic / drug effects

Substances

  • Carrier Proteins
  • DNA, Single-Stranded
  • DNA-Binding Proteins
  • Nuclear Proteins
  • TOPBP1 protein, human
  • Doxycycline