Cellular proteins bind to the downstream component of the lytic origin of DNA replication of Epstein-Barr virus

J Virol. 1995 Mar;69(3):1878-86. doi: 10.1128/JVI.69.3.1878-1886.1995.

Abstract

The lytic origin of DNA replication of Epstein-Barr virus, oriLyt, is a complex eukaryotic origin which is activated during the lytic phase of the viral life cycle. It consists of at least two independent cis-acting components, one of which plays a dual role in transcription and DNA replication. The binding of the viral factor BZLF1, a member of the AP1 family of transcription factors, to this upstream component is crucial for oriLyt function (A. Schepers, D. Pich, and W. Hammerschmidt, EMBO J. 12:3921-3929, 1993). The second cis-acting element, the downstream component of oriLyt, is equally indispensable; however, its function is unknown. In this study, the downstream component was found to be the binding target of several cellular proteins. One could be identified as Sp1 or as a related protein which binds twice to the downstream component of oriLyt. Mutational analysis indicated that Sp1 alone is not directly involved in mediating DNA replication; however, other factors which share the same binding sequence or bind closely to one of the Sp1 binding sites are likely candidates to contribute to a replication protein complex at the downstream component of oriLyt. The sequence requirements for the downstream component are remarkably stringent, indicating that at least one of the putative factors is a sequence-specific DNA-binding protein which is required for the activation of oriLyt.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA Replication*
  • DNA, Viral / metabolism*
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation, Viral
  • Herpesvirus 4, Human / genetics*
  • Humans
  • Hybrid Cells
  • In Vitro Techniques
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides / chemistry
  • Oligodeoxyribonucleotides / metabolism
  • Regulatory Sequences, Nucleic Acid*
  • Sp1 Transcription Factor / metabolism
  • Virus Replication*

Substances

  • DNA, Viral
  • DNA-Binding Proteins
  • Oligodeoxyribonucleotides
  • Sp1 Transcription Factor