B-Myb-dependent regulation of c-Myc expression by cytosolic phospholipase A2

J Biol Chem. 2004 Apr 23;279(17):17715-22. doi: 10.1074/jbc.M310561200. Epub 2004 Feb 9.

Abstract

Cytosolic phospholipase A(2) (cPLA(2)) cleaves membrane phospholipids to release arachidonic acid, initiating lipoxygenase and cyclooxygenase pathways. Mice lacking a gene for cPLA(2) suggested important roles of the protein in allergic responses, fertility, and neural cell death. Here we show that cPLA(2) negatively regulates c-Myc expression in a B-Myb-dependent manner. Overexpression of cPLA(2) protein but not a mutant cPLA(2) protein that lacks in vitro binding ability with B-Myb inhibits B-Myb-dependent c-myc gene expression. The inhibition was associated with physical interaction of B-Myb protein with cPLA(2) both in the cytoplasm and the nucleus. Binding site analysis demonstrated that both the N and C termini of cPLA(2) interact with B-Myb. Macrophage colony stimulating factor (MCSF) stimulated cPLA(2) redistribution into the nucleus and also association with B-Myb in human monocytes. Importantly, macrophages from mice with a disrupted cPLA(2) gene demonstrated significantly increased levels of c-Myc protein in the nucleus compared with cells from the wild-type mice, whereas B-Myb levels were similar in the cells from the cPLA(2)(+/+) and cPLA(2)(-/-) mice. Moreover, an introduction of cPLA(2) into cPLA(2)(-/-) mouse macrophages resulted in decreased c-Myc protein levels, and an inhibition of cPLA(2) expression by small interfering RNAs or antisense RNA increased the c-myc transcription in macrophage colony stimulating factor-activated human monocytes. These findings provide new insights into the function of cPLA(2) in B-Myb-dependent gene expression.

MeSH terms

  • Animals
  • Arachidonic Acid / metabolism
  • Binding Sites
  • Blotting, Western
  • Cell Cycle Proteins*
  • Cell Death
  • Cell Line
  • Cell Nucleus / metabolism
  • Cytoplasm / metabolism
  • DNA Damage
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation
  • Genes, Reporter
  • Humans
  • Hydrogen Peroxide / chemistry
  • Macrophage Colony-Stimulating Factor / metabolism
  • Macrophages / metabolism
  • Mice
  • Mice, Transgenic
  • Microscopy, Confocal
  • Microscopy, Fluorescence
  • Monocytes / metabolism
  • Phospholipases A / physiology*
  • Phospholipases A2
  • Plasmids / metabolism
  • Precipitin Tests
  • Protein Binding
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins c-myc / biosynthesis*
  • RNA, Antisense / metabolism
  • RNA, Small Interfering / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Subcellular Fractions
  • Time Factors
  • Trans-Activators / metabolism*
  • Ultraviolet Rays
  • Up-Regulation

Substances

  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • MYBL2 protein, human
  • Mybl2 protein, mouse
  • Proto-Oncogene Proteins c-myc
  • RNA, Antisense
  • RNA, Small Interfering
  • Trans-Activators
  • Arachidonic Acid
  • Macrophage Colony-Stimulating Factor
  • Hydrogen Peroxide
  • Phospholipases A
  • Phospholipases A2