Efficient expression of an Epstein-Barr nuclear antigen in Drosophila cells transfected with Epstein-Barr virus DNA

EMBO J. 1985 Nov;4(11):2955-9. doi: 10.1002/j.1460-2075.1985.tb04029.x.

Abstract

In a search for exogenous promoters which function in cultured Drosophila cells, we have co-transfected a D. melanogaster cell line with an Epstein-Barr virus (EBV) cosmid clone which encodes the Epstein-Barr nuclear antigen (EBNA-1). Here we report that Drosophila cells containing stably integrated copies of EBNA-1 encoding DNA synthesise a polypeptide of mol. wt. identical to that of authentic EBNA-1, which is detectable with EBNA-positive but not EBNA-negative human serum. As in EBV-transformed lymphoblastoid cells, this neo-antigen is associated with the nucleus of transfected cells suggesting that cellular localisation signals which operate in mammalian cells are also recognised in insect cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Viral / analysis
  • Antigens, Viral / genetics*
  • Cell Line
  • Cell Transformation, Viral
  • Cloning, Molecular
  • Cosmids
  • DNA Replication
  • Drosophila melanogaster / genetics*
  • Electrophoresis, Polyacrylamide Gel
  • Epstein-Barr Virus Nuclear Antigens
  • Herpesvirus 4, Human / genetics
  • Herpesvirus 4, Human / immunology*
  • Molecular Weight
  • Promoter Regions, Genetic
  • Transfection*

Substances

  • Antigens, Viral
  • Epstein-Barr Virus Nuclear Antigens