The periphery of nuclear domain 10 (ND10) as site of DNA virus deposition.
about
Virion assembly factories in the nucleus of polyomavirus-infected cellsDifferential regulation of sentrinized proteins by a novel sentrin-specific proteaseEBV tegument protein BNRF1 disrupts DAXX-ATRX to activate viral early gene transcriptionEvidence 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 expressionInteraction of the adenovirus type 5 E4 Orf3 protein with promyelocytic leukemia protein isoform II is required for ND10 disruption.Cellular localization, expression, and structure of the nuclear dot protein 52Viral immediate-early proteins abrogate the modification by SUMO-1 of PML and Sp100 proteins, correlating with nuclear body disruptionProteasome-independent disruption of PML oncogenic domains (PODs), but not covalent modification by SUMO-1, is required for human cytomegalovirus immediate-early protein IE1 to inhibit PML-mediated transcriptional repression.A 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 expressionAbility of the human cytomegalovirus IE1 protein to modulate sumoylation of PML correlates with its functional activities in transcriptional regulation and infectivity in cultured fibroblast cellsCovalent modification of the homeodomain-interacting protein kinase 2 (HIPK2) by the ubiquitin-like protein SUMO-1PML 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 genomesThe potential link between PML NBs and ICP0 in regulating lytic and latent infection of HSV-1An Adenovirus DNA Replication Factor, but Not Incoming Genome Complexes, Targets PML Nuclear Bodies.Dynamic Response of IFI16 and Promyelocytic Leukemia Nuclear Body Components to Herpes Simplex Virus 1 InfectionAdenovirus Early Proteins and Host SumoylationThe Role of Nuclear Antiviral Factors against Invading DNA Viruses: The Immediate Fate of Incoming Viral GenomesDegradation of nucleosome-associated centromeric histone H3-like protein CENP-A induced by herpes simplex virus type 1 protein ICP0The transcriptional role of PML and the nuclear bodyIdentification of three major sentrinization sites in PMLKaposi's sarcoma-associated herpesvirus K-Rta exhibits SUMO-targeting ubiquitin ligase (STUbL) like activity and is essential for viral reactivationAdenovirus type 5 early region 1B 55K oncoprotein-dependent degradation of cellular factor Daxx is required for efficient transformation of primary rodent cellsAdenovirus protein VII functions throughout early phase and interacts with cellular proteins SET and pp32ND10 components relocate to sites associated with herpes simplex virus type 1 nucleoprotein complexes during virus infection.Changing nuclear landscape and unique PML structures during early epigenetic transitions of human embryonic stem cells.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.Functional connection between Rad51 and PML in homology-directed repair.Proteomics of herpes simplex virus replication compartments: association of cellular DNA replication, repair, recombination, and chromatin remodeling proteins with ICP8.A dominant-negative herpesvirus protein inhibits intranuclear targeting of viral proteins: effects on DNA replication and late gene expression.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 isoformsAnalysis of HCF, the cellular cofactor of VP16, in herpes simplex virus-infected cells.Perturbation of cell cycle progression and cellular gene expression as a function of herpes simplex virus ICP0.
P2860
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P2860
The periphery of nuclear domain 10 (ND10) as site of DNA virus deposition.
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
The periphery of nuclear domain 10 (ND10) as site of DNA virus deposition.
@en
The periphery of nuclear domain 10
@nl
type
label
The periphery of nuclear domain 10 (ND10) as site of DNA virus deposition.
@en
The periphery of nuclear domain 10
@nl
prefLabel
The periphery of nuclear domain 10 (ND10) as site of DNA virus deposition.
@en
The periphery of nuclear domain 10
@nl
P2860
P356
P1476
The periphery of nuclear domain 10 (ND10) as site of DNA virus deposition.
@en
P2093
P2860
P304
P356
10.1083/JCB.134.4.815
P407
P577
1996-08-01T00:00:00Z