The pseudorabies virus UL28 protein enters the nucleus after coexpression with the herpes simplex virus UL15 protein

被引:39
作者
Koslowski, KM
Shaver, PR
Wang, XY
Tenney, DJ
Pederson, NE
机构
[1] E CAROLINA UNIV,SCH MED,DEPT MICROBIOL & IMMUNOL,GREENVILLE,NC 27858
[2] BRISTOL MYERS SQUIBB CO,PHARMACEUT RES INST,DEPT VIROL,WALLINGFORD,CT 06492
关键词
D O I
10.1128/JVI.71.12.9118-9123.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Herpesvirus DNA is packaged into capsids in the nuclei of infected cells in a process requiring at least six viral proteins. Of the proteins required for encapsidation of viral DNA, UL15 and UL28 are the most conserved among herpes simplex virus type 1 (HSV), varicella-zoster virus, and equine herpesvirus 1. The subcellular distribution of the pseudorabies virus (PRV) UL28 protein was examined by in situ immunofluorescence, UL28 was present in the nuclei of infected cells; however, UL28 was limited to the cytoplasm in the absence of other viral proteins. When cells expressing variant forms of UL28 were infected with a PRV UL28-null mutant, UL28 entered the nucleus, provided the carboxyl terminal 155 amino acids were present. Additionally, PRV UL28 entered the nucleus in cells infected with HSV. Two HSV packaging proteins were tested for the ability to affect the subcellular distribution of UL28, Coexpression of HSV UL15 enabled PRV UL28 to enter the nucleus in a manner that required the carboxyl-terminal 155 amino acids of UL28, Coexpression of HSV UL25 did not affect the distribution of UL28, We propose that an interaction between UL15 and UL28 facilitates the transport of a UL15-UL28 complex to the infected-cell nucleus.
引用
收藏
页码:9118 / 9123
页数:6
相关论文
共 27 条
[1]   HERPES-SIMPLEX VIRUS TYPE-1 UL28 GENE-PRODUCT IS IMPORTANT FOR THE FORMATION OF MATURE CAPSIDS [J].
ADDISON, C ;
RIXON, FJ ;
PRESTON, VG .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :2377-2384
[2]   THE HERPES-SIMPLEX VIRUS UL33 GENE-PRODUCT IS REQUIRED FOR THE ASSEMBLY OF FULL CAPSIDS [J].
ALKOBAISI, MF ;
RIXON, FJ ;
MCDOUGALL, I ;
PRESTON, VG .
VIROLOGY, 1991, 180 (01) :380-388
[3]   The U(L)15 gene of herpes simplex virus type 1 contains within its second exon a novel open reading frame that is translated in frame with the U(L)15 gene product [J].
Baines, JD ;
Cunningham, C ;
Nalwanga, D ;
Davison, A .
JOURNAL OF VIROLOGY, 1997, 71 (04) :2666-2673
[4]   THE HERPES-SIMPLEX VIRUS-1 U(L)15 GENE ENCODES 2 PROTEINS AND IS REQUIRED FOR CLEAVAGE OF GENOMIC VIRAL-DNA [J].
BAINES, JD ;
POON, APW ;
ROVNAK, J ;
ROIZMAN, B .
JOURNAL OF VIROLOGY, 1994, 68 (12) :8118-8124
[5]   LINKER-INSERTION NONSENSE AND RESTRICTION-SITE DELETION MUTATIONS OF GB-GLYCOPROTEIN GENE OF HERPES-SIMPLEX VIRUS TYPE-1 [J].
CAI, WH ;
PERSON, S ;
WARNER, SC ;
ZHOU, JH ;
DELUCA, NA .
JOURNAL OF VIROLOGY, 1987, 61 (03) :714-721
[6]   RESOLUTION OF GENOTYPIC AND PHENOTYPIC PROPERTIES OF HERPES-SIMPLEX VIRUS TYPE-1 TEMPERATURE-SENSITIVE MUTANT (KOS) TSZ47 - EVIDENCE FOR ALLELIC COMPLEMENTATION IN THE UL28 GENE [J].
CAVALCOLI, JD ;
BAGHIAN, A ;
HOMA, FL ;
KOUSOULAS, KG .
VIROLOGY, 1993, 197 (01) :23-34
[7]   NUCLEOTIDE-SEQUENCES OF HERPES-SIMPLEX VIRUS TYPE-1 (HSV-1) AFFECTING VIRUS ENTRY, CELL-FUSION, AND PRODUCTION OF GLYCOPROTEIN-GB (VP7) [J].
DELUCA, N ;
BZIK, DJ ;
BOND, VC ;
PERSON, S ;
SNIPES, W .
VIROLOGY, 1982, 122 (02) :411-423
[8]   Enzymatic characterization of hepatitis C virus NS3/4A complexes expressed in mammalian cells by using the herpes simplex virus amplicon system [J].
Hong, Z ;
Ferrari, E ;
WrightMinogue, J ;
Chase, R ;
Risano, C ;
Seelig, G ;
Lee, CG ;
Kwong, AD .
JOURNAL OF VIROLOGY, 1996, 70 (07) :4261-4268
[9]   A SHORT AMINO-ACID SEQUENCE ABLE TO SPECIFY NUCLEAR LOCATION [J].
KALDERON, D ;
ROBERTS, BL ;
RICHARDSON, WD ;
SMITH, AE .
CELL, 1984, 39 (03) :499-509
[10]   THE VIRULENCE-DETERMINING GENOMIC BAMHI FRAGMENT-4 OF PSEUDORABIES VIRUS CONTAINS GENES CORRESPONDING TO THE U(L)15 (PARTIAL), U(L)18, U(L)19, U(L)20, AND U(L)21 GENES OF HERPES-SIMPLEX VIRUS AND A PUTATIVE ORIGIN OF REPLICATION [J].
KLUPP, BG ;
KERN, H ;
METTENLEITER, TC .
VIROLOGY, 1992, 191 (02) :900-908