Expression of the first 811 nucleotides of the herpes simplex virus type 1 latency-associated transcript (LAT) partially restores wild-type spontaneous reactivation to a LAT-null mutant

被引:24
作者
Drolet, BS
Perng, GC
Viliosis, RJ
Slanina, SM
Nesburn, AB
Wechsler, SL
机构
[1] Cedars Sinai Med Ctr, Burns & Allen Res Inst, Ophthalmol Res Labs, Los Angeles, CA 90048 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Ophthalmol, Los Angeles, CA 90024 USA
关键词
D O I
10.1006/viro.1998.9492
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The herpes simplex virus type 1 (HSV-1) latency-associated transcript (LAT) gene is required for efficient spontaneous reactivation in the rabbit ocular model. We recently showed that insertion of 1.8 kb of the LAT promoter and the first 1.5 kb of the 8.3-kb primary LAT transcript into a novel, ectopic location in the virus unique long (UL) region restored wild-type spontaneous reactivation to a LAT-null mutant To further map the LAT spontaneous reactivation function within the first 1.5 kb of LAT, we rescued the same LAT-null mutant by inserting 1.8 kb of the LAT promoter and just the first 811 nucleotides of LAT into the same location in the UL. In a series of three experiments, the resulting virus, designated LAT2.6A, had a spontaneous reactivation rate that was midway between the original LAT-null mutant and wild-type virus, Thus expression of the first 811 LAT nucleotides produced a spontaneous reactivation rate that was significantly higher than that of the LAT-null mutant but significantly less than that of wild type. This suggests that part but not all, of the LAT function involved in efficient spontaneous reactivation is located within the first 811 nucleotides of the primary 8.3-kb LAT, (C) 1999 Academic Press.
引用
收藏
页码:96 / 106
页数:11
相关论文
共 30 条
[1]   A HERPES-SIMPLEX VIRUS TYPE-1 LATENCY-ASSOCIATED TRANSCRIPT MUTANT REACTIVATES WITH NORMAL KINETICS FROM LATENT INFECTION [J].
BLOCK, TM ;
SPIVACK, JG ;
STEINER, I ;
DESHMANE, S ;
MCINTOSH, MT ;
LIRETTE, RP ;
FRASER, NW .
JOURNAL OF VIROLOGY, 1990, 64 (07) :3417-3426
[2]   MOLECULAR ANALYSIS OF HERPES-SIMPLEX VIRUS TYPE-1 DURING EPINEPHRINE-INDUCED REACTIVATION OF LATENTLY INFECTED-RABBITS IN-VIVO [J].
BLOOM, DC ;
DEVIRAO, GB ;
HILL, JM ;
STEVENS, JG ;
WAGNER, EK .
JOURNAL OF VIROLOGY, 1994, 68 (03) :1283-1292
[3]   The region of the herpes simplex virus type 1 LAT gene involved in spontaneous reactivation does not encode a functional protein [J].
Drolet, BS ;
Perng, GC ;
Cohen, J ;
Slanina, SM ;
Yukht, A ;
Nesburn, AB ;
Wechsler, SL .
VIROLOGY, 1998, 242 (01) :221-232
[4]   HERPES-SIMPLEX VIRUS LATENCY-ASSOCIATED TRANSCRIPT IS A STABLE INTRON [J].
FARRELL, MJ ;
DOBSON, AT ;
FELDMAN, LT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :790-794
[5]   ANALYSIS OF THE HERPES-SIMPLEX VIRUS TYPE-1 PROMOTER CONTROLLING THE EXPRESSION OF UL38, A TRUE LATE GENE INVOLVED IN CAPSID ASSEMBLY [J].
FLANAGAN, WM ;
PAPAVASSILIOU, AG ;
RICE, M ;
HECHT, LB ;
SILVERSTEIN, S ;
WAGNER, EK .
JOURNAL OF VIROLOGY, 1991, 65 (02) :769-786
[6]   ADRENERGICALLY INDUCED RECURRENT HSV-1 CORNEAL EPITHELIAL LESIONS [J].
HILL, JM ;
HARUTA, Y ;
ROOTMAN, DS .
CURRENT EYE RESEARCH, 1987, 6 (08) :1065-1071
[7]   HERPES-SIMPLEX VIRUS LATENT PHASE TRANSCRIPTION FACILITATES INVIVO REACTIVATION [J].
HILL, JM ;
SEDARATI, F ;
JAVIER, RT ;
WAGNER, EK ;
STEVENS, JG .
VIROLOGY, 1990, 174 (01) :117-125
[8]   HERPES-SIMPLEX VIRUS LATENT RNA (LAT) IS NOT REQUIRED FOR LATENT INFECTION IN THE MOUSE [J].
HO, DY ;
MOCARSKI, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (19) :7596-7600
[9]   A HERPES-SIMPLEX VIRUS TRANSCRIPT ABUNDANT IN LATENTLY INFECTED NEURONS IS DISPENSABLE FOR ESTABLISHMENT OF THE LATENT STATE [J].
JAVIER, RT ;
STEVENS, JG ;
DISSETTE, VB ;
WAGNER, EK .
VIROLOGY, 1988, 166 (01) :254-257
[10]   THE CONTROL OF HERPES-SIMPLEX VIRUS TYPE-1 LATE GENE-TRANSCRIPTION - A 'TATA-BOX'/CAP SITE REGION IS SUFFICIENT FOR FULLY EFFICIENT REGULATED ACTIVITY [J].
JOHNSON, PA ;
EVERETT, RD .
NUCLEIC ACIDS RESEARCH, 1986, 14 (21) :8247-8264