KSHV RTA utilizes the host E3 ubiquitin ligase complex RNF20/40 to drive lytic reactivation

J Virol. 2023 Nov 30;97(11):e0138923. doi: 10.1128/jvi.01389-23. Epub 2023 Oct 27.

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) is a cancer-causing human herpesvirus that establishes a persistent infection in humans. The lytic viral cycle plays a crucial part in lifelong infection as it is involved in the viral dissemination. The master regulator of the KSHV lytic replication cycle is the viral replication and transcription activator (RTA) protein, which is necessary and sufficient to push the virus from latency into the lytic phase. Thus, the identification of host factors utilized by RTA for controlling the lytic cycle can help to find novel targets that could be used for the development of antiviral therapies against KSHV. Using a proteomics approach, we have identified a novel interaction between RTA and the cellular E3 ubiquitin ligase complex RNF20/40, which we have shown to be necessary for promoting RTA-induced KSHV lytic cycle.

Keywords: BCBL1; E3 ubiquitin ligases; Kaposi's sarcoma-associated herpesvirus; RNF20 and RNF40; RTA; gene regulation; lytic reactivation.

MeSH terms

  • Herpesvirus 8, Human* / growth & development
  • Herpesvirus 8, Human* / physiology
  • Host Microbial Interactions*
  • Humans
  • Immediate-Early Proteins* / metabolism
  • Protein Binding
  • Proteomics
  • Trans-Activators / metabolism
  • Ubiquitin-Protein Ligases* / metabolism
  • Viral Proteins* / metabolism
  • Virus Activation*
  • Virus Latency*
  • Virus Replication*

Substances

  • Immediate-Early Proteins
  • RNF20 protein, human
  • RNF40 protein, human
  • Rta protein, Human herpesvirus 8
  • Trans-Activators
  • Ubiquitin-Protein Ligases
  • Viral Proteins
  • ORF 50 transactivator