Gene-specific transactivation by herpes simplex virus type 1 alpha protein ICP27.
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Herpes simplex virus ICP27 protein directly interacts with the nuclear pore complex through Nup62, inhibiting host nucleocytoplasmic transport pathwaysHerpes simplex virus IE63 (ICP27) protein interacts with spliceosome-associated protein 145 and inhibits splicing prior to the first catalytic stepVaricella-zoster virus open reading frame 61 protein is functionally homologous to herpes simplex virus type 1 ICP0Herpes simplex virus type 1 immediate-early protein ICP27 is required for efficient incorporation of ICP0 and ICP4 into virionsHerpes simplex virus type 1 entry is inhibited by the cobalt chelate complex CTC-96Analysis of the phosphorylation sites of herpes simplex virus type 1 regulatory protein ICP27.Control of VP16 translation by the herpes simplex virus type 1 immediate-early protein ICP27.HSV-1 ICP27 induces apoptosis by promoting Bax translocation to mitochondria through interacting with 14-3-3θ.HSV-1 ICP27 represses NF-κB activity by regulating Daxx sumoylationPersistence and expression of the herpes simplex virus genome in the absence of immediate-early proteins.The human herpesvirus 8 homolog of Epstein-Barr virus SM protein (KS-SM) is a posttranscriptional activator of gene expressionHerpes simplex virus ICP27 induces cytoplasmic accumulation of unspliced polyadenylated alpha-globin pre-mRNA in infected HeLa cells.Processing of alpha-globin and ICP0 mRNA in cells infected with herpes simplex virus type 1 ICP27 mutants.Herpes simplex virus ICP27 activation of stress kinases JNK and p38.Identification and transcriptional analyses of the UL3 and UL4 genes of equine herpesvirus 1, homologs of the ICP27 and glycoprotein K genes of herpes simplex virus.Herpes simplex virus ICP27 protein provides viral mRNAs with access to the cellular mRNA export pathway.Up to four distinct polypeptides are produced from the γ34.5 open reading frame of herpes simplex virus 2Direct stimulation of translation by the multifunctional herpesvirus ICP27 protein.Mapping of functional regions in the amino-terminal portion of the herpes simplex virus ICP27 regulatory protein: importance of the leucine-rich nuclear export signal and RGG Box RNA-binding domain.The early expression of glycoprotein B from herpes simplex virus can be detected by antigen-specific CD8+ T cells.Proteomic analysis of the herpes simplex virus 1 virion protein 16 transactivator protein in infected cellsIntracellular localization of the herpes simplex virus type 1 major transcriptional regulatory protein, ICP4, is affected by ICP27Evaluation of colocalization interactions between the IE110, IE175, and IE63 transactivator proteins of herpes simplex virus within subcellular punctate structuresIdentification of nuclear and nucleolar localization signals in the herpes simplex virus regulatory protein ICP27.Regulatory function of the equine herpesvirus 1 ICP27 gene product.Two overlapping transcription units which extend across the L-S junction of herpes simplex virus type 1.Identification of ribonucleotide reductase mutation causing temperature-sensitivity of herpes simplex virus isolates from whitlow by deep sequencing.Functional interactions between herpes simplex virus immediate-early proteins during infection: gene expression as a consequence of ICP27 and different domains of ICP4.An activity specified by the osteosarcoma line U2OS can substitute functionally for ICP0, a major regulatory protein of herpes simplex virus type 1Herpes simplex virus trans-regulatory protein ICP27 stabilizes and binds to 3' ends of labile mRNA.Herpes simplex ICP27 mutant viruses exhibit reduced expression of specific DNA replication genesRepression of the alpha0 gene by ICP4 during a productive herpes simplex virus infection.Overexpression of the herpes simplex virus type 1 immediate-early regulatory protein, ICP27, is responsible for the aberrant localization of ICP0 and mutant forms of ICP4 in ICP4 mutant virus-infected cells.Prolonged gene expression and cell survival after infection by a herpes simplex virus mutant defective in the immediate-early genes encoding ICP4, ICP27, and ICP22.Human cytomegalovirus tegument protein pp71 (ppUL82) enhances the infectivity of viral DNA and accelerates the infectious cycle.The herpes simplex virus immediate-early protein ICP0 affects transcription from the viral genome and infected-cell survival in the absence of ICP4 and ICP27A LAT-associated function reduces productive-cycle gene expression during acute infection of murine sensory neurons with herpes simplex virus type 1.Varicella-zoster virus open reading frame 4 encodes an immediate-early protein with posttranscriptional regulatory propertiesMutational analysis of the herpes simplex virus type 1 ICP0 C3HC4 zinc ring finger reveals a requirement for ICP0 in the expression of the essential alpha27 gene.Rapid cytotoxic T lymphocyte activation occurs in the draining lymph nodes after cutaneous herpes simplex virus infection as a result of early antigen presentation and not the presence of virus
P2860
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P2860
Gene-specific transactivation by herpes simplex virus type 1 alpha protein ICP27.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
Gene-specific transactivation by herpes simplex virus type 1 alpha protein ICP27.
@en
type
label
Gene-specific transactivation by herpes simplex virus type 1 alpha protein ICP27.
@en
prefLabel
Gene-specific transactivation by herpes simplex virus type 1 alpha protein ICP27.
@en
P2860
P1433
P1476
Gene-specific transactivation by herpes simplex virus type 1 alpha protein ICP27.
@en
P2093
P2860
P304
P407
P577
1988-10-01T00:00:00Z