Ablation of Go alpha-subunit results in a transformed phenotype and constitutively active phosphatidylcholine-specific phospholipase C

J Biol Chem. 1997 Jul 11;272(28):17312-9. doi: 10.1074/jbc.272.28.17312.

Abstract

Modulation of the components involved in mitogenic signaling cascades is critical to the regulation of cell growth. GTP-binding proteins and the stimulation of phosphatidylcholine (PC) hydrolysis have been shown to play major roles in these cascades. One of the enzymes involved in PC hydrolysis, a PC-specific phospholipase C (PC-PLC) has received relatively little attention. In this paper we examined the role of a particular heterotrimeric GTP-binding protein, Go, in the regulation of cell growth and PC-PLC-mediated hydrolysis of PC in IIC9 fibroblasts. The Go alpha-subunit was ablated in IIC9 cells by stable expression of antisense RNA. These stably transfected cells acquired a transformed phenotype as indicated by: (a) the formation of multiple foci in monolayer cultures, (b) the acquisition of anchorage-independent growth in soft agar; and (c) an increased level of thymidine incorporation in the absence of added mitogens. These data implicate Goalpha as a novel tumor suppressor. Interestingly, PC-PLC activity was constitutively active in the Goalpha-ablated cells as evidenced by the chronically elevated levels of diacylglycerol and phosphorylcholine in the absence of growth factors. In contrast, basal activities of PC-phospholipase D, phospholipase A2, or phosphoinositol-PLC were not affected. These data demonstrate, for the first time, a role for Go in regulating cell growth and provide definitive evidence for the existence of a PC-PLC in eukaryotic cells. The data further indicate that a subunit of Go, is involved in regulating this enzyme.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Division
  • Cell Transformation, Neoplastic*
  • Choline Kinase / metabolism
  • Cricetinae
  • Cricetulus
  • Diglycerides / metabolism
  • Enzyme Activation
  • GTP-Binding Protein alpha Subunits, Gi-Go
  • GTP-Binding Proteins / genetics
  • GTP-Binding Proteins / physiology*
  • Humans
  • Oligonucleotides, Antisense / metabolism
  • Phenotype
  • Phosphatidate Phosphatase / metabolism
  • Phosphatidylcholines / metabolism
  • Phosphatidylinositols / metabolism
  • Phospholipase D / metabolism
  • Phospholipases A / metabolism
  • Phospholipases A2
  • Rats
  • Transducin / pharmacology
  • Type C Phospholipases / metabolism*

Substances

  • Diglycerides
  • Oligonucleotides, Antisense
  • Phosphatidylcholines
  • Phosphatidylinositols
  • Choline Kinase
  • Phospholipases A
  • Phospholipases A2
  • Phosphatidate Phosphatase
  • Type C Phospholipases
  • phosphatidylcholine-specific phospholipase C
  • Phospholipase D
  • GTP-Binding Proteins
  • GTP-Binding Protein alpha Subunits, Gi-Go
  • Transducin