Kaposi's sarcoma-associated herpesvirus/human herpesvirus 8 RTA reactivates murine gammaherpesvirus 68 from latency

J Virol. 2005 Mar;79(5):3217-22. doi: 10.1128/JVI.79.5.3217-3222.2005.

Abstract

Murine gammaherpesvirus 68 (MHV-68), Kaposi's sarcoma-associated herpesvirus (HHV-8), and Epstein-Barr virus (EBV) are all members of the gammaherpesvirus family, characterized by their ability to establish latency in lymphocytes. The RTA protein, conserved in all gammaherpesviruses, is known to play a critical role in reactivation from latency. Here we report that HHV-8 RTA, not EBV RTA, was able to induce MHV-68 lytic viral proteins and DNA replication and processing and produce viable MHV-68 virions from latently infected cells at levels similar to those for MHV-68 RTA. HHV-8 RTA was also able to activate two MHV-68 lytic promoters, whereas EBV RTA was not. In order to define the domains of RTA responsible for their functional differences in viral promoter activation and initiation of the MHV-68 lytic cycle, chimeric RTA proteins were constructed by exchanging the N-terminal and C-terminal domains of the RTA proteins. Our data suggest that the species specificity of MHV-68 RTA resides in the N-terminal DNA binding domain.

Publication types

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

MeSH terms

  • Animals
  • Herpesvirus 4, Human / genetics
  • Herpesvirus 4, Human / physiology
  • Herpesvirus 8, Human / genetics*
  • Herpesvirus 8, Human / physiology*
  • Humans
  • Immediate-Early Proteins / chemistry
  • Immediate-Early Proteins / genetics*
  • Immediate-Early Proteins / physiology*
  • Protein Structure, Tertiary
  • Rhadinovirus / genetics*
  • Rhadinovirus / physiology*
  • Species Specificity
  • Trans-Activators / chemistry
  • Trans-Activators / genetics*
  • Trans-Activators / physiology*
  • Viral Proteins / chemistry
  • Viral Proteins / genetics*
  • Viral Proteins / physiology*
  • Virus Activation / genetics
  • Virus Activation / physiology
  • Virus Latency / genetics
  • Virus Latency / physiology

Substances

  • BRLF1 protein, Human herpesvirus 4
  • Immediate-Early Proteins
  • Rta protein, Human herpesvirus 8
  • Trans-Activators
  • Viral Proteins