The null mutant of the U(L)31 gene of herpes simplex virus 1: Construction and phenotype in infected cells

被引:77
作者
Chang, YE
VanSant, C
Krug, PW
Sears, AE
Roizman, B
机构
[1] UNIV CHICAGO, MARJORIE B KOVLER VIRAL ONCOL LABS, CHICAGO, IL 60637 USA
[2] EMORY UNIV, SCH MED, DEPT MICROBIOL & IMMUNOL, ATLANTA, GA 30322 USA
关键词
D O I
10.1128/JVI.71.11.8307-8315.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Earlier studies have shown that the U(L)31 protein is homogeneously distributed throughout the nucleus and cofractionates with nuclear matrix, We report the construction from an appropriate cosmid library a deletion mutant which replicates in rabbit skin cells carrying the U(L)31 gene under a late (gamma(1)) viral promoter, The mutant virus exhibits cytopathic effects and yields 0.01 to 0.1% of the yield of wild-type parent virus in noncomplementing cells but amounts of virus 10- to 1,000-fold higher than those recovered from the same cells 3 h after infection, Electron microscopic studies indicate the presence of small numbers of full capsids but a lack of enveloped virions, Viral DNA extracted from the cytoplasm of infected cells exhibits free termini indicating cleavage/packaging of viral DNA from concatemers for packaging into virions, but analyses of viral DNAs by pulsed-field electrophoresis indicate that at 16 h after infection, both the yields of viral DNA and cleavage of viral DNA for packaging are decreased, The repaired virus cannot be differentiated from the wild-type parent. These results suggest the possibility that U(L)31 protein forms a network to enable the anchorage of viral products for the synthesis and/or packaging of viral DNA into virions.
引用
收藏
页码:8307 / 8315
页数:9
相关论文
共 36 条
[1]   HERPES-SIMPLEX VIRUS AND PROTEIN-TRANSPORT ARE ASSOCIATED WITH THE CYTOSKELETAL FRAMEWORK AND THE NUCLEAR MATRIX IN INFECTED BSC-1 CELLS [J].
BENZEEV, A ;
ABULAFIA, R ;
BRATOSIN, S .
VIROLOGY, 1983, 129 (02) :501-507
[2]   THE NUCLEAR MATRIX - A HEURISTIC MODEL FOR INVESTIGATING GENOMIC ORGANIZATION AND FUNCTION IN THE CELL-NUCLEUS [J].
BEREZNEY, R .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1991, 47 (02) :109-123
[3]   INSITU LOCALIZATION OF THE MAJOR CAPSID PROTEIN DURING LYTIC INFECTION BY HERPES-SIMPLEX VIRUS [J].
BIBORHARDY, V ;
DAGENAIS, A ;
SIMARD, R .
JOURNAL OF GENERAL VIROLOGY, 1985, 66 (APR) :897-901
[4]   THE NUCLEAR MATRIX IS INVOLVED IN HERPES-SIMPLEX VIROGENESIS [J].
BIBORHARDY, V ;
POUCHELET, M ;
STPIERRE, E ;
HERZBERG, M ;
SIMARD, R .
VIROLOGY, 1982, 121 (02) :296-306
[5]   NUCLEAR MATRIX MODIFICATIONS AT DIFFERENT STAGES OF INFECTION BY HERPES-SIMPLEX VIRUS TYPE-1 [J].
BIBORHARDY, V ;
BERNARD, M ;
SIMARD, R .
JOURNAL OF GENERAL VIROLOGY, 1985, 66 (MAY) :1095-1103
[6]  
BLAHO JA, 1994, J BIOL CHEM, V269, P17401
[7]  
Carrol SB, 1987, DNA CLONING PRACTICA, V3, P89
[8]   THE PRODUCT OF THE U(L)31 GENE OF HERPES-SIMPLEX VIRUS-1 IS A NUCLEAR PHOSPHORPROTEIN WHICH PARTITIONS WITH THE NUCLEAR MATRIX [J].
CHANG, YE ;
ROIZMAN, B .
JOURNAL OF VIROLOGY, 1993, 67 (11) :6348-6356
[9]   Properties of the protein encoded by the U(L)32 open reading frame of herpes simplex virus 1 [J].
Chang, YJE ;
Poon, APW ;
Roizman, B .
JOURNAL OF VIROLOGY, 1996, 70 (06) :3938-3946
[10]  
CHANG YS, UNPUB