Nuclear domain 10 as preexisting potential replication start sites of herpes simplex virus type-1.
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ICP0 dismantles microtubule networks in herpes simplex virus-infected cellsVirion assembly factories in the nucleus of polyomavirus-infected cellsSequestration and inhibition of Daxx-mediated transcriptional repression by PMLFunctional interaction between class II histone deacetylases and ICP0 of herpes simplex virus type 1PML contributes to a cellular mechanism of repression of herpes simplex virus type 1 infection that is inactivated by ICP0Evidence for a role of the cellular ND10 protein PML in mediating intrinsic immunity against human cytomegalovirus infectionsDifferential role of Sp100 isoforms in interferon-mediated repression of herpes simplex virus type 1 immediate-early protein expressionViral immediate-early proteins abrogate the modification by SUMO-1 of PML and Sp100 proteins, correlating with nuclear body disruptionComponents of the REST/CoREST/histone deacetylase repressor complex are disrupted, modified, and translocated in HSV-1-infected cellsA novel ubiquitin-specific protease is dynamically associated with the PML nuclear domain and binds to a herpesvirus regulatory proteinA novel ubiquitin-specific protease is dynamically associated with the PML nuclear domain and binds to a herpesvirus regulatory proteinEpstein-Barr virus (EBV) SM protein induces and recruits cellular Sp110b to stabilize mRNAs and enhance EBV lytic gene expressionPML is critical for ND10 formation and recruits the PML-interacting protein daxx to this nuclear structure when modified by SUMO-1Functional inaccessibility of quiescent herpes simplex virus genomesRole of ND10 nuclear bodies in the chromatin repression of HSV-1Infected cell protein 0 functional domains and their coordination in herpes simplex virus replicationA comparison of herpes simplex virus type 1 and varicella-zoster virus latency and reactivationThe potential link between PML NBs and ICP0 in regulating lytic and latent infection of HSV-1Dynamic Response of IFI16 and Promyelocytic Leukemia Nuclear Body Components to Herpes Simplex Virus 1 InfectionTranscriptional activation of the adenoviral genome is mediated by capsid protein VIPML interaction with p53 and its role in apoptosis and replicative senescenceHSV-1 ICP0: paving the way for viral replicationKaposi's sarcoma-associated herpesvirus K-Rta exhibits SUMO-targeting ubiquitin ligase (STUbL) like activity and is essential for viral reactivationND10 components relocate to sites associated with herpes simplex virus type 1 nucleoprotein complexes during virus infection.Herpesviruses carrying a Brainbow cassette reveal replication and expression of limited numbers of incoming genomesVisualization by live-cell microscopy of disruption of ND10 during herpes simplex virus type 1 infection.Recruitment of cellular recombination and repair proteins to sites of herpes simplex virus type 1 DNA replication is dependent on the composition of viral proteins within prereplicative sites and correlates with the induction of the DNA damage respoA dominant-negative herpesvirus protein inhibits intranuclear targeting of viral proteins: effects on DNA replication and late gene expression.Herpes simplex virus tegument ICP0 is capsid associated, and its E3 ubiquitin ligase domain is important for incorporation into virions.Herpes simplex virus VP16, but not ICP0, is required to reduce histone occupancy and enhance histone acetylation on viral genomes in U2OS osteosarcoma cells.Disruption of PML subnuclear domains by the acidic IE1 protein of human cytomegalovirus is mediated through interaction with PML and may modulate a RING finger-dependent cryptic transactivator function of PMLThe papillomavirus minor capsid protein, L2, induces localization of the major capsid protein, L1, and the viral transcription/replication protein, E2, to PML oncogenic domainsHerpes simplex virus DNA packaging without measurable DNA synthesis.Persistence and expression of the herpes simplex virus genome in the absence of immediate-early proteins.The disruption of ND10 during herpes simplex virus infection correlates with the Vmw110- and proteasome-dependent loss of several PML isoformsPurification and characterization of a cellular protein that binds to the downstream activation sequence of the strict late UL38 promoter of herpes simplex virus type 1Analysis of HCF, the cellular cofactor of VP16, in herpes simplex virus-infected cells.Interactions of herpes simplex virus type 1 with ND10 and recruitment of PML to replication compartments.Evaluation of interactions of human cytomegalovirus immediate-early IE2 regulatory protein with small ubiquitin-like modifiers and their conjugation enzyme Ubc9Accumulation and intranuclear distribution of unintegrated human immunodeficiency virus type 1 DNA.
P2860
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P2860
Nuclear domain 10 as preexisting potential replication start sites of herpes simplex virus type-1.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Nuclear domain 10 as preexisti ...... f herpes simplex virus type-1.
@en
type
label
Nuclear domain 10 as preexisti ...... f herpes simplex virus type-1.
@en
prefLabel
Nuclear domain 10 as preexisti ...... f herpes simplex virus type-1.
@en
P2093
P356
P1433
P1476
Nuclear domain 10 as preexisti ...... f herpes simplex virus type-1.
@en
P2093
P356
10.1006/VIRO.1996.0094
P407
P577
1996-03-01T00:00:00Z