Identification of cellular proteins associated with human cytomegalovirus (HCMV) DNA replication suggests novel cellular and viral interactions

Virology. 2022 Jan:566:26-41. doi: 10.1016/j.virol.2021.11.004. Epub 2021 Nov 22.

Abstract

Upon entry of Human cytomegalovirus (HCMV) into the host cell, the viral genome is transported to the nucleus where it serves as a template for transcription and genome replication. Production of new viral genomes is a coordinated effort between viral and cellular proteins. While the core replication proteins are encoded by the virus, additional cellular proteins support the process of genome synthesis. We used accelerated native isolation of proteins on nascent DNA (aniPOND) to study protein dynamics on nascent viral DNA during HCMV infection. Using this method, we identified specific viral and cellular proteins that are associated with nascent viral DNA. These included transcription factors, transcriptional regulators, DNA damage and repair factors, and chromatin remodeling complexes. The association of these identified proteins with viral DNA was confirmed by immunofluorescent imaging, chromatin-immunoprecipitation analyses, and shRNA knockdown experiments. These data provide evidence for the requirement of cellular factors involved in HCMV replication.

Keywords: 5-Ethynyl-2′-deoxyuridine (EdU); DNA synthesis; Human cytomegalovirus (HCMV); Nascent viral DNA; aniPOND.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Proteins / classification
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Cell Line, Transformed
  • Cell Nucleus / genetics
  • Cell Nucleus / metabolism
  • Cell Nucleus / virology
  • Cytomegalovirus / genetics*
  • Cytomegalovirus / growth & development
  • Cytomegalovirus / metabolism
  • Cytoskeletal Proteins / classification
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Cytosol / metabolism
  • Cytosol / virology
  • DNA, Viral / genetics
  • DNA, Viral / metabolism
  • Fibroblasts / metabolism*
  • Fibroblasts / virology
  • Gene Expression Regulation
  • Gene Ontology
  • Genome, Viral*
  • Histones / classification
  • Histones / genetics
  • Histones / metabolism
  • Host-Pathogen Interactions / genetics*
  • Humans
  • Molecular Sequence Annotation
  • Ribosomal Proteins / classification
  • Ribosomal Proteins / genetics
  • Ribosomal Proteins / metabolism
  • Signal Transduction
  • Transcription Factors / classification
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Viral Proteins / classification
  • Viral Proteins / genetics*
  • Viral Proteins / metabolism
  • Virus Replication

Substances

  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • DNA, Viral
  • Histones
  • Ribosomal Proteins
  • Transcription Factors
  • Viral Proteins