The periphery of nuclear domain 10 (ND10) as site of DNA virus deposition

被引:298
作者
Ishov, AM [1 ]
Maul, GG [1 ]
机构
[1] WISTAR INST ANAT & BIOL,PHILADELPHIA,PA 19104
关键词
D O I
10.1083/jcb.134.4.815
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
After DNA viruses enter the nucleus, they initiate a transcriptional cascade which is followed by replication. We investigated whether these processes take place at specific nuclear sites or, as suggested by the mode of entry, randomly throughout the nucleus. Three distinct nuclear domains, nuclear factor-1 sites, coiled bodies, and nuclear domain 10 (ND10), were used as markers to investigate the relative position of DNA virus replication sites, We found that all three nuclear domains had a very high spatial correlation with each other in uninfected cells, After adenoviral infection, nuclear factor 1 and coiled bodies were found associated with some viral replication domains, Simian virus 40 begins replication adjacent to ND10 but adenovirus 5 and herpes simplex type 1 modified ND10s before replication. Adenovirus E4orf 3 gene deletion mutants retain ND10 and begin replication at the peripheries of ND10. The same was found for the herpes simplex virus type 1 immediate early gene 1 mutants, That the deposition and replication of adenovirus 5 and herpesvirus type 1 at ND10 was not a mutant phenotype was confirmed by finding the input wild-type virus juxtaposed to ND10, The transport of viral genomes to ND10 does not require viral gene expression, Thus, the peripheries of ND10 represent preferred sites where early steps of transcription and replication of at least three DNA virus families take place, suggesting a new set of functional properties for this large nuclear domain.
引用
收藏
页码:815 / 826
页数:12
相关论文
共 68 条
[1]   IDENTIFICATION OF A NOVEL NUCLEAR DOMAIN [J].
ASCOLI, CA ;
MAUL, GG .
JOURNAL OF CELL BIOLOGY, 1991, 112 (05) :785-795
[2]   ADENOVIRUS TYPE-5 EARLY REGION-1B GENE-PRODUCT IS REQUIRED FOR EFFICIENT SHUTOFF OF HOST PROTEIN-SYNTHESIS [J].
BABISS, LE ;
GINSBERG, HS .
JOURNAL OF VIROLOGY, 1984, 50 (01) :202-212
[3]   MOLECULAR-GENETICS OF HERPES-SIMPLEX VIRUS .8. FURTHER CHARACTERIZATION OF A TEMPERATURE-SENSITIVE MUTANT DEFECTIVE IN RELEASE OF VIRAL-DNA AND IN OTHER STAGES OF THE VIRAL REPRODUCTIVE-CYCLE [J].
BATTERSON, W ;
FURLONG, D ;
ROIZMAN, B .
JOURNAL OF VIROLOGY, 1983, 45 (01) :397-407
[4]  
BERKNER KL, 1992, CURR TOP MICROBIOL, V158, P39
[5]   NUCLEAR FACTOR-I IS SPECIFICALLY TARGETED TO DISCRETE SUBNUCLEAR SITES IN ADENOVIRUS TYPE-2-INFECTED CELLS [J].
BOSHER, J ;
DAWSON, A ;
HAY, RT .
JOURNAL OF VIROLOGY, 1992, 66 (05) :3140-3150
[6]   NUCLEAR-BODIES (NBS) - A NEWLY REDISCOVERED ORGANELLE [J].
BRASCH, K ;
OCHS, RL .
EXPERIMENTAL CELL RESEARCH, 1992, 202 (02) :211-223
[7]   NUCLEAR-ORGANIZATION OF SPLICING SMALL NUCLEAR RIBONUCLEOPROTEINS IN ADENOVIRUS-INFECTED CELLS [J].
BRIDGE, E ;
CARMOFONSECA, M ;
LAMOND, A ;
PETTERSSON, U .
JOURNAL OF VIROLOGY, 1993, 67 (10) :5792-5802
[8]   REDUNDANT CONTROL OF ADENOVIRUS LATE GENE-EXPRESSION BY EARLY REGION-4 [J].
BRIDGE, E ;
KETNER, G .
JOURNAL OF VIROLOGY, 1989, 63 (02) :631-638
[9]   CONSTRUCTION, CHARACTERIZATION, AND UTILIZATION OF CELL-LINES WHICH INDUCIBLY EXPRESS THE ADENOVIRUS DNA-BINDING PROTEIN [J].
BROUGH, DE ;
CLEGHON, V ;
KLESSIG, DF .
VIROLOGY, 1992, 190 (02) :624-634
[10]   TRANSCRIPTION-DEPENDENT COLOCALIZATION OF THE U1, U2, U4/U6, AND U5 SNRNPS IN COILED BODIES [J].
CARMOFONSECA, M ;
PEPPERKOK, R ;
CARVALHO, MT ;
LAMOND, AI .
JOURNAL OF CELL BIOLOGY, 1992, 117 (01) :1-14