DNA replication checkpoint promotes G1-S transcription by inactivating the MBF repressor Nrm1

Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11230-5. doi: 10.1073/pnas.0801106105. Epub 2008 Aug 5.

Abstract

The cell cycle transcriptional program imposes order on events of the cell-cycle and is a target for signals that regulate cell-cycle progression, including checkpoints required to maintain genome integrity. Neither the mechanism nor functional significance of checkpoint regulation of the cell-cycle transcription program are established. We show that Nrm1, an MBF-specific transcriptional repressor acting at the transition from G(1) to S phase of the cell cycle, is at the nexus between the cell cycle transcriptional program and the DNA replication checkpoint in fission yeast. Phosphorylation of Nrm1 by the Cds1 (Chk2) checkpoint protein kinase, which is activated in response to DNA replication stress, promotes its dissociation from the MBF transcription factor. This leads to the expression of genes encoding components that function in DNA replication and repair pathways important for cell survival in response to arrested DNA replication.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Checkpoint Kinase 2
  • DNA Repair / physiology
  • DNA Replication / physiology*
  • DNA, Fungal / genetics
  • DNA, Fungal / metabolism*
  • G1 Phase / physiology*
  • Genome, Fungal / physiology
  • Phosphorylation
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • S Phase / physiology*
  • Schizosaccharomyces / genetics
  • Schizosaccharomyces / metabolism*
  • Schizosaccharomyces pombe Proteins / genetics
  • Schizosaccharomyces pombe Proteins / metabolism*

Substances

  • DNA, Fungal
  • Nrm1 protein, S pombe
  • Repressor Proteins
  • Schizosaccharomyces pombe Proteins
  • Checkpoint Kinase 2
  • Cds1 protein, S pombe
  • Protein Serine-Threonine Kinases