Nuclear translocation of phospholipase C-delta1 is linked to the cell cycle and nuclear phosphatidylinositol 4,5-bisphosphate

J Biol Chem. 2005 Jun 10;280(23):22060-9. doi: 10.1074/jbc.M413813200. Epub 2005 Apr 4.

Abstract

Nuclear phosphoinositides, especially phosphatidylinositol 4,5-bisphosphate, fluctuate throughout the cell cycle and are linked to proliferation and differentiation. Here we report that phospholipase C-delta(1) accumulates in the nucleus at the G(1)/S boundary and in G(0) phases of the cell cycle. Furthermore, as wild-type protein accumulated in the nucleus, nuclear phosphatidylinositol 4,5-bisphosphate levels were elevated 3-5-fold, whereas total levels were decreased compared with asynchronous cultures. To test whether phosphatidylinositol 4,5-bisphosphate binding is important during this process, we introduced a R40D point mutation within the pleckstrin homology domain of phospholipase C-delta(1), which disables high affinity phosphatidylinositol 4,5-bisphosphate binding, and found that nuclear translocation was significantly reduced at G(1)/S and in G(0). These results demonstrate a cell cycle-dependent compartmentalization of phospholipase C-delta(1) and support the idea that relative levels of phosphoinositides modulate the portioning of phosphoinositide-binding proteins between the nucleus and other compartments.

MeSH terms

  • Active Transport, Cell Nucleus*
  • Animals
  • Blotting, Western
  • Cell Cycle
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Nucleus / metabolism*
  • Cell Proliferation
  • Chromatography, Thin Layer
  • Cytoplasm / metabolism
  • DNA, Complementary / metabolism
  • Detergents / pharmacology
  • Fibroblasts / metabolism
  • Flow Cytometry
  • Fluorescent Antibody Technique, Indirect
  • G1 Phase
  • Glioma / metabolism
  • Green Fluorescent Proteins / metabolism
  • Humans
  • Image Processing, Computer-Assisted
  • Isoenzymes / chemistry*
  • Isoenzymes / metabolism*
  • Lipid Metabolism
  • Mice
  • Microscopy, Fluorescence
  • Models, Biological
  • NIH 3T3 Cells
  • Phosphatidylinositol 4,5-Diphosphate / metabolism*
  • Phospholipase C delta
  • Point Mutation
  • Protein Structure, Tertiary
  • Protein Transport
  • Resting Phase, Cell Cycle
  • S Phase
  • Subcellular Fractions
  • Time Factors
  • Transfection
  • Type C Phospholipases / chemistry*
  • Type C Phospholipases / metabolism*

Substances

  • DNA, Complementary
  • Detergents
  • Isoenzymes
  • Phosphatidylinositol 4,5-Diphosphate
  • Green Fluorescent Proteins
  • Type C Phospholipases
  • PLCD1 protein, human
  • Phospholipase C delta
  • Plcd1 protein, mouse