The cellular protein Daxx interacts with avian sarcoma virus integrase and viral DNA to repress viral transcription

被引:52
作者
Greger, JG
Katz, RA
Ishov, AM
Maul, GG
Skalka, AM
机构
[1] Fox Chase Canc Ctr, Inst Canc Res, Philadelphia, PA 19111 USA
[2] Univ Penn, Sch Med, Grad Grp Cell & Mol Biol, Philadelphia, PA 19104 USA
[3] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
关键词
D O I
10.1128/JVI.79.8.4610-4618.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The cellular protein Daxx was identified as an interactor with avian sarcoma virus (ASV) integrase (IN) in a yeast two-hybrid screen. After infection, Daxx-IN interactions were detected by coinummoprecipitation. An association between Daxx and viral DNA, likely mediated by IN, was also detected by chromatin immunoprecipitation. Daxx was not required for early events in ASV replication, including integration, as Daxx-null cells were transduced as efficiently as Daxx-expressing cells. However, viral reporter gene expression from ASV-based vectors was substantially higher in the Daxx-null cells than in Daxx-complemented cells. Consistent with this observation, histone deacetylases (HDACs) were found to associate with viral DNA in Daxx-complemented cells but not in Daxx-null cells. Furthermore, Daxx protein was induced in an interferon-like manner upon ASV infection. We conclude that Daxx interacts with an IN-viral DNA complex early after infection and may mediate the repression of viral gene expression via the recruitment of HDACs. Our findings provide a novel example of cellular immunity against viral replication in which viral transcription is repressed via the recruitment of antiviral proteins to the viral DNA.
引用
收藏
页码:4610 / 4618
页数:9
相关论文
共 47 条
[41]   Mouse cytomegalovirus immediate-early protein 1 binds with host cell repressors to relieve suppressive effects on viral transcription and replication during lytic infection [J].
Tang, QY ;
Maul, GG .
JOURNAL OF VIROLOGY, 2003, 77 (02) :1357-1367
[42]   Human Daxx regulates Fas-induced apoptosis from nuclear PML oncogenic domains (PODs) [J].
Torii, S ;
Egan, DA ;
Evans, RA ;
Reed, JC .
EMBO JOURNAL, 1999, 18 (21) :6037-6049
[43]   Cytoplasmic recruitment of INI1 and PML on incoming HIV preintegration complexes: Interference with early steps of viral replication [J].
Turelli, P ;
Doucas, V ;
Craig, E ;
Mangeat, B ;
Klages, N ;
Evans, R ;
Kalpana, G ;
Trono, D .
MOLECULAR CELL, 2001, 7 (06) :1245-1254
[44]   Daxx, a novel Fas-binding protein that activates JNK and apoptosis [J].
Yang, XL ;
KhosraviFar, R ;
Chang, HY ;
Baltimore, D .
CELL, 1997, 89 (07) :1067-1076
[45]   Inhibition of HIV-1 virion production by a transdominant mutant of integrase interactor 1 [J].
Yung, E ;
Sorin, M ;
Pal, A ;
Craig, E ;
Morozov, A ;
Delattre, O ;
Kappes, J ;
Oti, D ;
Kalpana, GV .
NATURE MEDICINE, 2001, 7 (08) :920-926
[46]   Studies on the morphology and taxonomy of three new myxosporeans of the genus Sinuolinea Davis, 1917 (Myxosporea: Sinuolineidae) infecting the urinary bladder of some marine fishes from the Shandong coast, China [J].
Zhao, YJ ;
Song, WB .
SYSTEMATIC PARASITOLOGY, 2003, 55 (01) :53-59
[47]   Interferon action in triply deficient mice reveals the existence of alternative antiviral pathways [J].
Zhou, AM ;
Paranjape, JM ;
Der, SD ;
Williams, BRG ;
Silverman, RH .
VIROLOGY, 1999, 258 (02) :435-440