Synthesis of thymidine kinase (TK) in Epstein-Barr virus-superinfected Raji TK-negative cells

Intervirology. 1981;15(1):43-8. doi: 10.1159/000149213.

Abstract

Epstein-Barr virus (EBV) from P3HR-1 cells, but not from B95-8 cells, can induce the synthesis of thymidine kinase (TK) in TK-negative Raji cells. The synthesis of TK was slightly reduced, but not inhibited, when cells were cultivated in the presence of cytosine arabinoside (ara-C). On the other hand, the synthesis of TK in ordinary Raji cells was enhanced in the presence of the drug. Thymidine-beta-D-arabinofuranoside (ara-T) was capable of reducing the conversion rate of thymidine to TdR nucleotides by extracts prepared from superinfected Raji TK-cells, but had no influence on TK activity in cell extracts from ordinary Raji cells and EBV-negative Ramos cells. This suggested a broader substrate specificity of the virally induced enzyme.

Publication types

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

MeSH terms

  • Arabinonucleosides / pharmacology
  • Cell Line
  • Cytarabine / pharmacology
  • Enzyme Induction
  • Herpesvirus 4, Human / enzymology*
  • Herpesvirus 4, Human / growth & development
  • Humans
  • Substrate Specificity
  • Thymidine / analogs & derivatives
  • Thymidine / pharmacology
  • Thymidine Kinase / biosynthesis*

Substances

  • Arabinonucleosides
  • Cytarabine
  • Thymidine Kinase
  • thymine arabinoside
  • Thymidine