Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
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Herpes simplex virus type 1 immediate-early protein ICP27 is required for efficient incorporation of ICP0 and ICP4 into virionsThe degradation of promyelocytic leukemia and Sp100 proteins by herpes simplex virus 1 is mediated by the ubiquitin-conjugating enzyme UbcH5aInfected cell protein 0 functional domains and their coordination in herpes simplex virus replicationPosttranslational processing of infected cell proteins 0 and 4 of herpes simplex virus 1 is sequential and reflects the subcellular compartment in which the proteins localizeThe stability of herpes simplex virus 1 ICP0 early after infection is defined by the RING finger and the UL13 protein kinase.The U(S)3 protein kinase blocks apoptosis induced by the d120 mutant of herpes simplex virus 1 at a premitochondrial stage.cdc2 cyclin-dependent kinase binds and phosphorylates herpes simplex virus 1 U(L)42 DNA synthesis processivity factorRequirements for the nuclear-cytoplasmic translocation of infected-cell protein 0 of herpes simplex virus 1Herpes simplex virus 1-infected cell protein 0 contains two E3 ubiquitin ligase sites specific for different E2 ubiquitin-conjugating enzymesNovel roles of cytoplasmic ICP0: proteasome-independent functions of the RING finger are required to block interferon-stimulated gene production but not to promote viral replication.Characterization of the novel E3 ubiquitin ligase encoded in exon 3 of herpes simplex virus-1-infected cell protein 0.Interwoven roles of cyclin D3 and cdk4 recruited by ICP0 and ICP4 in the expression of herpes simplex virus genesHerpes simplex virus immediate-early ICP0 protein inhibits Toll-like receptor 2-dependent inflammatory responses and NF-kappaB signalingHerpes simplex virus 1 mutant in which the ICP0 HUL-1 E3 ubiquitin ligase site is disrupted stabilizes cdc34 but degrades D-type cyclins and exhibits diminished neurotoxicityOverexpression of promyelocytic leukemia protein precludes the dispersal of ND10 structures and has no effect on accumulation of infectious herpes simplex virus 1 or its proteinsThe herpes simplex virus immediate-early ubiquitin ligase ICP0 induces degradation of the ICP0 repressor protein E2FBP1.The promyelocytic leukemia nuclear body: sites of activity?Herpes simplex virus protein kinase US3 activates and functionally overlaps protein kinase A to block apoptosisRole of ICP0 in the strategy of conquest of the host cell by herpes simplex virus 1The herpes simplex virus type 1 BgKL variant, unlike the BgOL variant, shows a higher association with orolabial infection than with infections at other sites, supporting the variant-dispersion-replacement hypothesis.Translocation and colocalization of ICP4 and ICP0 in cells infected with herpes simplex virus 1 mutants lacking glycoprotein E, glycoprotein I, or the virion host shutoff product of the UL41 gene.Use of biotinylated plasmid DNA as a surrogate for HSV DNA to identify proteins that repress or activate viral gene expression.Herpes simplex virus 1 gene expression is accelerated by inhibitors of histone deacetylases in rabbit skin cells infected with a mutant carrying a cDNA copy of the infected-cell protein no. 0.The infected cell protein 0 of herpes simplex virus 1 dynamically interacts with proteasomes, binds and activates the cdc34 E2 ubiquitin-conjugating enzyme, and possesses in vitro E3 ubiquitin ligase activity.ICP0 enables and monitors the function of D cyclins in herpes simplex virus 1 infected cells.During its nuclear phase the multifunctional regulatory protein ICP0 undergoes proteolytic cleavage characteristic of polyproteins.Activities of ICP0 involved in the reversal of silencing of quiescent herpes simplex virus 1.A protein encoded by the herpes simplex virus (HSV) type 1 2-kilobase latency-associated transcript is phosphorylated, localized to the nucleus, and overcomes the repression of expression from exogenous promoters when inserted into the quiescent HSVHerpes simplex virus type 1 immediate-early protein ICP0 and is isolated RING finger domain act as ubiquitin E3 ligases in vitro.Herpes simplex virus type 1 regulatory protein ICP0 does not protect cyclins D1 and D3 from degradation during infection.Recruitment of herpes simplex virus type 1 immediate-early protein ICP0 to the virus particle.Relaxed repression of herpes simplex virus type 1 genomes in Murine trigeminal neuronsTiming Is Everything.
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P2860
Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
description
2001 nî lūn-bûn
@nan
2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
@ast
Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
@en
type
label
Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
@ast
Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
@en
prefLabel
Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
@ast
Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
@en
P2093
P2860
P1433
P1476
Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.
@en
P2093
P2860
P304
P356
10.1128/JVI.75.4.1888-1898.2001
P577
2001-02-01T00:00:00Z