共 40 条
TRANSCRIPTIONAL ANALYSIS OF THE HERPES-SIMPLEX VIRUS TYPE-1 REGION CONTAINING THE TR(L)-U(L) JUNCTION
被引:33
作者:

SINGH, J
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF IRVINE,DEPT MOLEC BIOL & BIOCHEM,IRVINE,CA 92717

WAGNER, EK
论文数: 0 引用数: 0
h-index: 0
机构: UNIV CALIF IRVINE,DEPT MOLEC BIOL & BIOCHEM,IRVINE,CA 92717
机构:
[1] UNIV CALIF IRVINE,DEPT MOLEC BIOL & BIOCHEM,IRVINE,CA 92717
[2] UNIV CALIF IRVINE,PROGRAM ANIM VIROL,IRVINE,CA 92717
来源:
关键词:
D O I:
10.1006/viro.1993.1470
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
In this study we have used a combination of Northern blot, cDNA, and RNAse protection analysis to characterize transcription occurring at the junction of the long terminal repeat (TRL) and long unique segment (UL) of herpes simplex virus type 1 (HSV-1). Two low abundance 5′ colinear transcripts mapped between the junction of the TRL/UL and the cap site of the primary latency associated transcripts (LAT). Analysis of the region containing the first four open translational reading frames (ORFs) of the UL segment of the virus revealed a complex pattern of overlapping transcripts and polyadenylation site utilization. Inefficient termination late, but not early in infection, at the polyadenylation site following the UL2 ORF leads to an unusual situation where the promoter controlling a βγ transcript encoding the UL1 ORF also controls a 5′ colinear γ transcript. Further, although the entire UL3 ORF is conserved between HSV-1 and HSV-2, the only abundant uniquely UL3 encoding transcript in both virus types was found to originate within the UL3 ORF and has the capacity to encode only a truncated UL3 protein product. © 1993 Academic Press. All rights reserved.
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页码:220 / 231
页数:12
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