The IE2 60-Kilodalton and 40-Kilodalton Proteins Are Dispensable for Human Cytomegalovirus Replication but Are Required for Efficient Delayed Early and Late Gene Expression and Production of Infectious Virus

Antzeko izenburuak

• Human Cytomegalovirus IE2 86 and IE2 40 Proteins Differentially Regulate UL84 Protein Expression Posttranscriptionally in the Absence of Other Viral Gene Products
  nork: Sanders, Rebecca L., et al.
  Argitaratua: (2010)
• Mutation of Glutamine to Arginine at Position 548 of IE2 86 in Human Cytomegalovirus Leads to Decreased Expression of IE2 40, IE2 60, UL83, and UL84 and Increased Transcription of US8-9 and US29-32
  nork: Burgdorf, Sarah W., et al.
  Argitaratua: (2011)
• Internal Deletions of IE2 86 and Loss of the Late IE2 60 and IE2 40 Proteins Encoded by Human Cytomegalovirus Affect the Levels of UL84 Protein but Not the Amount of UL84 mRNA or the Loading and Distribution of the mRNA on Polysomes
  nork: Sanders, Rebecca L., et al.
  Argitaratua: (2008)
• Development of Cell Lines That Provide Tightly Controlled Temporal Translation of the Human Cytomegalovirus IE2 Proteins for Complementation and Functional Analyses of Growth-Impaired and Nonviable IE2 Mutant Viruses
  nork: Sanders, Rebecca L., et al.
  Argitaratua: (2008)
• The Canonical Immediate Early 3 Gene Product pIE611 of Mouse Cytomegalovirus Is Dispensable for Viral Replication but Mediates Transcriptional and Posttranscriptional Regulation of Viral Gene Products
  nork: Rattay, Stephanie, et al.
  Argitaratua: (2015)