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Mutational analysis of varicella-zoster virus (VZV) immediate early protein (IE62) subdomains and their importance in viral replication.
Khalil, Mohamed I; Che, Xibing; Sung, Phillip; Sommer, Marvin H; Hay, John; Arvin, Ann M.
Affiliation
  • Khalil MI; Departments of Pediatrics and Microbiology & Immunology, Stan ford University School of Medicine, Stanford, CA, United States; Department of Molecular Biology, National Research Centre, El-Buhouth St., Cairo, Egypt. Electronic address: mkhalil2@stanford.edu.
  • Che X; Departments of Pediatrics and Microbiology & Immunology, Stan ford University School of Medicine, Stanford, CA, United States.
  • Sung P; Departments of Pediatrics and Microbiology & Immunology, Stan ford University School of Medicine, Stanford, CA, United States.
  • Sommer MH; Departments of Pediatrics and Microbiology & Immunology, Stan ford University School of Medicine, Stanford, CA, United States.
  • Hay J; Department of Microbiology and Immunology, School of Medicine and Biomedical Science, University at Buffalo, Buffalo, NY, United States.
  • Arvin AM; Departments of Pediatrics and Microbiology & Immunology, Stan ford University School of Medicine, Stanford, CA, United States.
Virology ; 492: 82-91, 2016 May.
Article in En | MEDLINE | ID: mdl-26914506
ABSTRACT
VZV IE62 is an essential, immediate-early, tegument protein and consists of five domains. We generated recombinant viruses carrying mutations in the first three IE62 domains and tested their influence on VZV replication kinetics. The mutations in domain I did not affect replication kinetics while domain II mutations, disrupting the DNA binding and dimerization domain (DBD), were lethal for VZV replication. Mutations in domain III of the nuclear localization signal (NLS) and the two phosphorylation sites S686A/S722A resulted in slower growth in early and late infection respectively and were associated with IE62 accumulation in the cytoplasm and nucleus respectively. This study mapped the functional domains of IE62 in context of viral infection, indicating that DNA binding and dimerization domain is essential for VZV replication. In addition, the correct localization of IE62, whether nuclear or cytoplasmic, at different points in the viral life cycle, is important for normal progression of VZV replication.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Replication / Trans-Activators / Viral Envelope Proteins / Reassortant Viruses / Immediate-Early Proteins / Herpesvirus 3, Human / Nuclear Localization Signals Limits: Humans Language: En Journal: Virology Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Replication / Trans-Activators / Viral Envelope Proteins / Reassortant Viruses / Immediate-Early Proteins / Herpesvirus 3, Human / Nuclear Localization Signals Limits: Humans Language: En Journal: Virology Year: 2016 Document type: Article