DRG2 Regulates G2/M Progression via the Cyclin B1-Cdk1 Complex

Mol Cells. 2016 Sep;39(9):699-704. doi: 10.14348/molcells.2016.0149. Epub 2016 Sep 27.

Abstract

Developmentally regulated GTP-binding protein 2 (DRG2) plays an important role in cell growth. Here we explored the linkage between DRG2 and G2/M phase checkpoint function in cell cycle progression. We observed that knockdown of DRG2 in HeLa cells affected growth in a wound-healing assay, and tumorigenicity in nude mice xenografts. Flow cytometry assays and [(3)H] incorporation assays indicated that G2/M phase arrest was responsible for the decreased proliferation of these cells. Knockdown of DRG2 elicited down-regulation of the major mitotic promoting factor, the cyclin B1/Cdk1 complex, but up-regulation of the cell cycle arresting proteins, Wee1, Myt1, and p21. These findings identify a novel role of DRG2 in G2/M progression.

Keywords: DRG2; G2/M check point; cyclin B/Cdk1 complex; p21.

MeSH terms

  • Animals
  • CDC2 Protein Kinase
  • Cell Proliferation / physiology
  • Cyclin B1 / genetics
  • Cyclin B1 / metabolism
  • Cyclin B1 / physiology*
  • Cyclin-Dependent Kinases / genetics
  • Cyclin-Dependent Kinases / metabolism
  • Cyclin-Dependent Kinases / physiology*
  • G2 Phase Cell Cycle Checkpoints / physiology*
  • GTP-Binding Proteins / genetics
  • GTP-Binding Proteins / metabolism
  • GTP-Binding Proteins / physiology*
  • Gene Knockdown Techniques
  • HeLa Cells
  • Heterografts
  • Humans
  • Male
  • Mice
  • Mice, Nude
  • Mitosis / physiology

Substances

  • CCNB1 protein, human
  • Cyclin B1
  • DRG2 protein, human
  • CDC2 Protein Kinase
  • CDK1 protein, human
  • Cyclin-Dependent Kinases
  • GTP-Binding Proteins