RRM1 maintains centrosomal integrity via CHK1 and CDK1 signaling during replication stress

Cancer Lett. 2014 May 1;346(2):249-56. doi: 10.1016/j.canlet.2013.12.031. Epub 2014 Jan 14.

Abstract

DNA lesion-induced centrosomal abnormalities during the replication phase are relatively unknown. Here, we report that RNAi-mediated depletion of RRM1 induces cell-cycle arrest at the replication phase, along with severe DNA damage and centrosomal amplification. Interestingly, CHK1 depletion synergistically increased RRM1-depletion-induced centrosomal amplification. In response to hydroxyurea, CHK1 was delocalized from the centrosome by RRM1 depletion. Moreover, CDK1, which functions in centrosome separation and is inhibited by CHK1, was found to be essential for RRMI1-depletion-induced centrosomal amplification. Thus, we herein demonstrate that RRM1 preserves chromosomal stability via the CHK1- and CDK1-dependent stabilization of the centrosomal integrity at the replication stage.

Keywords: Centrosome integrity; DNA damage; RRM1; Replication fork stalling; Tumor suppressor; Tumorigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CDC2 Protein Kinase / genetics
  • CDC2 Protein Kinase / metabolism*
  • Cell Line, Tumor
  • Centrosome / metabolism
  • Centrosome / physiology*
  • Checkpoint Kinase 1
  • Cyclin A / metabolism
  • Cyclin B / metabolism
  • DNA Damage
  • DNA Replication / genetics
  • DNA Replication / physiology*
  • Gene Knockdown Techniques
  • HeLa Cells
  • Humans
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • RNA, Small Interfering / administration & dosage
  • RNA, Small Interfering / genetics
  • Ribonucleoside Diphosphate Reductase
  • Signal Transduction
  • Transfection
  • Tumor Suppressor Proteins / deficiency
  • Tumor Suppressor Proteins / genetics*
  • Tumor Suppressor Proteins / metabolism

Substances

  • Cyclin A
  • Cyclin B
  • RNA, Small Interfering
  • Tumor Suppressor Proteins
  • RRM1 protein, human
  • Ribonucleoside Diphosphate Reductase
  • Protein Kinases
  • CHEK1 protein, human
  • Checkpoint Kinase 1
  • CDC2 Protein Kinase