Herpes simplex virus type-1: A model for genome transactions

被引:9
作者
Boehmer, PE
Villani, G
机构
[1] Univ Miami, Sch Med, Dept Biochem & Mol Biol, Miami, FL 33101 USA
[2] CNRS, UMR 5089, Inst Pharmacol & Biol Struct, F-31077 Toulouse 4, France
来源
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 75 | 2003年 / 75卷
关键词
D O I
10.1016/S0079-6603(03)75005-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In many respects, HSV-1 is the prototypic herpes virus. However, HSV-1 also serves as an excellent model system to study genome transactions, including DNA replication, homologous recombination, and the interaction of DNA replication enzymes with DNA damage. Like eukaryotic chromosomes, the HSV-1 genome contains multiple origins of replication. Replication of the HSV-1 genome is mediated by the concerted action of several virus-encoded proteins that are thought to assemble into a multiprotein complex. Several host-encoded factors have also been implicated in viral DNA replication. Furthermore, replication of the HSV-1 genome is known to be closely associated with homologous recombination that, like in many cellular organisms, may function in recombinational repair. Finally, recent data have shed some light on the interaction of essential HSV-1 replication proteins, specifically its DNA polymerase and DNA helicases, with damaged DNA. © 2003 Elsevier Science. © 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:139 / 171
页数:33
相关论文
共 120 条
[1]   THE ORIGIN-BINDING DOMAIN OF THE HERPES-SIMPLEX VIRUS TYPE-1 UL9 PROTEIN IS NOT REQUIRED FOR DNA HELICASE ACTIVITY [J].
ABBOTTS, AP ;
STOW, ND .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :3125-3130
[2]   Modulation of the herpes simplex virus type-1 UL9 DNA helicase by its cognate single-strand DNA-binding protein, ICP8 [J].
Arana, ME ;
Haq, B ;
Le Gac, NT ;
Boehmer, PE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (09) :6840-6845
[3]   ATP-dependent unwinding of a minimal origin of DNA replication by the origin-binding protein and the single-strand DNA-binding protein ICP8 from Herpes simplex virus type I [J].
Aslani, A ;
Olsson, M ;
Elias, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (43) :41204-41212
[4]   Complementary intrastrand base pairing during initiation of herpes simplex virus type 1 DNA replication [J].
Aslani, A ;
Macao, B ;
Simonsson, S ;
Elias, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (13) :7194-7199
[5]   Purification and characterization of OF-1, a host factor implicated in herpes simplex replication [J].
Baker, RO ;
Murata, LB ;
Dodson, MS ;
Hall, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (39) :30050-30057
[6]   TRANSCRIPTIONAL ANALYSIS OF THE REGION OF THE HERPES-SIMPLEX VIRUS TYPE-1 GENOME CONTAINING THE UL8, UL9, AND UL10 GENES AND IDENTIFICATION OF A NOVEL DELAYED-EARLY GENE-PRODUCT, OBPC [J].
BARADARAN, K ;
DABROWSKI, CE ;
SCHAFFER, PA .
JOURNAL OF VIROLOGY, 1994, 68 (07) :4251-4261
[7]   Inhibition of a DNA-helicase by peptide nucleic acids [J].
Bastide, L ;
Boehmer, PE ;
Villani, G ;
Lebleu, B .
NUCLEIC ACIDS RESEARCH, 1999, 27 (02) :551-554
[8]   DNA cleavage and packaging proteins encoded by genes UL28, UL15, and UL33 of herpes simplex virus type 1 form a complex in infected cells [J].
Beard, PM ;
Taus, NS ;
Baines, JD .
JOURNAL OF VIROLOGY, 2002, 76 (10) :4785-4791
[9]   Herpes virus replication [J].
Boehmer, PE ;
Nimonkar, AV .
IUBMB LIFE, 2003, 55 (01) :13-22
[10]   The herpes simplex virus type-1 single-strand DNA-binding protein, ICP8, increases the processivity of the UL9 protein DNA helicase [J].
Boehmer, PE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (05) :2676-2683