Herpes simplex virus type 1 UL14 tegument protein regulates intracellular compartmentalization of major tegument protein VP16

Akane Ohta, Yohei Yamauchi, Yoshifumi Muto, Hiroshi Kimura, Yukihiro Nishiyama

Research output: Contribution to journalArticle (Academic Journal)peer-review

9 Citations (Scopus)


BACKGROUND: Herpes simplex virus type 1 (HSV-1) has a complicated life-cycle, and its genome encodes many components that can modify the cellular environment to facilitate efficient viral replication. The protein UL14 is likely involved in viral maturation and egress (Cunningham C. et al), and it facilitates the nuclear translocation of viral capsids and the tegument protein VP16 during the immediate-early phase of infection (Yamauchi Y. et al, 2008). UL14 of herpes simplex virus type 2 exhibits multiple functions (Yamauchi Y. et al, 2001, 2002, 2003).

METHODS: To better understand the function(s) of UL14, we generated VP16-GFP-incorporated UL14-mutant viruses with either single (K51M) or triple (R60A, R64A, E68D) amino acid substitutions in the heat shock protein (HSP)-like sequence of UL14. We observed the morphology of cells infected with UL14-null virus and amino acid-substituted UL14-mutant viruses at different time points after infection.

RESULTS: UL14(3P)-VP16GFP and UL14D-VP16GFP (UL14-null) viruses caused similar defects with respect to growth kinetics, compartmentalization of tegument proteins, and cellular morphology in the late phase. Both the UL14D-VP16GFP and UL14(3P)-VP16GFP viruses led to the formation of an aggresome that incorporated some tegument proteins but did not include nuclear-egressed viral capsids.

CONCLUSIONS: Our findings suggest that a cluster of charged residues within the HSP-like sequence of UL14 is important for the molecular chaperone-like functions of UL14, and this activity is required for the acquisition of functionality of VP16 and UL46. In addition, UL14 likely contributes to maintaining cellular homeostasis following infection, including cytoskeletal organization. However, direct interactions between UL14 and VP16, UL46, or other cellular or viral proteins remain unclear.

Original languageEnglish
Pages (from-to)365
JournalVirology Journal
Publication statusPublished - 26 Jul 2011


  • Amino Acid Sequence
  • Amino Acid Substitution
  • Animals
  • Antigens, Viral
  • Cell Line
  • Cercopithecus aethiops
  • Cytoskeleton
  • Fibroblasts
  • Genes, Reporter
  • Green Fluorescent Proteins
  • Herpes Simplex Virus Protein Vmw65
  • Herpesvirus 1, Human
  • Host-Pathogen Interactions
  • Humans
  • Molecular Sequence Data
  • Mutant Proteins
  • Rabbits
  • Recombinant Fusion Proteins
  • Sequence Homology, Amino Acid
  • Viral Proteins
  • Journal Article
  • Research Support, Non-U.S. Gov't


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