Enhanced transcription of the s-adenosylhomocysteine hydrolase gene precedes Epstein-Barr virus lytic gene activation in ganglioside-stimulated lymphoma cells

Med Microbiol Immunol. 2000 Sep;189(1):13-8. doi: 10.1007/pl00008252.

Abstract

Stimulation of Epstein-Barr virus (EBV) genome-positive Burkitt lymphoma cells with the ganglioside IV3NeuAc-nLcOse4Cer leads to the induction of cell differentiation processes and activates the EBV lytic viral cycle. In cells of the Burkitt lymphoma line Raji differential expression of host cell genes was analysed in the early phase (150 min) post stimulation with the ganglioside to display the cell activities that precede the activation of the EBV lytic cycle using the differential display reverse transcription-polymerase chain reaction technique. Multiple fragment cDNAs derived from control cells and ganglioside-stimulated cells were amplified using random primers and displayed via polyacrylamide gel electrophoresis. The expression pattern of 8,400 bands was analysed. Eleven differentially expressed fragment cDNAs were reamplified and identified by nucleotide sequencing. Six of these could be identified as coding for proteins that may take part in virus reactivation and differentiation. The most striking finding was the induction of s-adenosylhomocysteine hydrolase (AHCY) expression. The cellular enzyme AHCY plays an important role in transmethylation reactions controlling the replication of several viruses. Thus. an involvement in EBV replication can be suggested.

Publication types

  • Comparative Study

MeSH terms

  • Adenosylhomocysteinase
  • Cell Cycle
  • Cell Line, Transformed
  • DNA, Complementary / analysis
  • DNA, Viral / genetics
  • Gangliosides / pharmacology*
  • Gene Expression Regulation, Enzymologic / drug effects
  • Herpesvirus 4, Human / drug effects
  • Herpesvirus 4, Human / genetics*
  • Humans
  • Hydrolases / biosynthesis
  • Hydrolases / genetics*
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcriptional Activation
  • Virus Activation

Substances

  • DNA, Complementary
  • DNA, Viral
  • Gangliosides
  • RNA, Messenger
  • Hydrolases
  • Adenosylhomocysteinase