HCMV UL8 interaction with β-catenin and DVL2 regulates viral reactivation in CD34+ hematopoietic progenitor cells

J Virol. 2023 Oct 31;97(10):e0124123. doi: 10.1128/jvi.01241-23. Epub 2023 Sep 29.

Abstract

CD34+ hematopoietic progenitor cells (HPCs) are an important cellular reservoir for latent human cytomegalovirus (HCMV). Several HCMV genes are expressed during latency that are involved with the maintenance of the viral genome in CD34+ HPC. However, little is known about the process of viral reactivation in these cells. Here, we describe a viral protein, pUL8, and its interaction and stabilization with members of the Wnt/β-catenin pathway as an important component of viral reactivation. We further define that pUL8 and β-catenin interact with DVL2 via a PDZ-binding domain, and loss of UL8 interaction with β-catenin-DVL2 restricts viral reactivation. Our findings will be instrumental in understanding the molecular processes involved in HCMV reactivation in order to design new antiviral therapeutics.

Keywords: UL8; Wnt signaling; human cytomegalovirus; viral reactivation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antigens, CD34* / metabolism
  • Cytomegalovirus* / genetics
  • Cytomegalovirus* / physiology
  • Dishevelled Proteins* / chemistry
  • Dishevelled Proteins* / metabolism
  • Hematopoietic Stem Cells* / metabolism
  • Hematopoietic Stem Cells* / virology
  • Humans
  • PDZ Domains
  • Viral Proteins* / chemistry
  • Viral Proteins* / metabolism
  • Virus Activation*
  • Virus Latency / genetics
  • beta Catenin* / chemistry
  • beta Catenin* / metabolism

Substances

  • Antigens, CD34
  • beta Catenin
  • Dishevelled Proteins
  • DVL2 protein, human
  • Viral Proteins