ANALYSIS OF THE HSV-1 STRAIN 17-DNA POLYMERASE GENE REVEALS THE EXPRESSION OF 4 DIFFERENT CLASSES OF POL TRANSCRIPTS

被引:9
作者
BLUDAU, H
FREESE, UK
机构
[1] Institut für Virusforschung, Deutsches krebsforschungszentrum, Im Neuenheimer Feld 280
关键词
D O I
10.1016/0042-6822(91)90980-P
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have investigated the structure and the expression of transcripts of the HSV-1 strain 17 DNA polymerase gene (pol) by various mapping methods including cDNA cloning. The majority of mature pol transcripts is strictly colinear with the pol gene. But additionally, pol cDNAs show a defined heterogeneity in respect to their 5′-terminal regions and can be divided into four classes with characteristics differences: (i) class 1 represents the major transcript (pol-R1) with initiation at HSV-1 positions 62,605-62,610, (ii) class 2 initiates about 70 bp downstream, (iii) class 3 is generated by splicing the short open reading frame (SORF) to a 5′-truncated part of the long open reading frame (LORF) which results in a partially different coding potential, and (iv) class 4 starts 120 bp upstream of the major iniation site in the central part of the origin of replication (oriL). S1 and Exo VII nuclease and RNase protection assays as well as primer extension analyses confirm the classification regarding the genuine structure of pol mRNAs and the differential usage of transcriptional start sites. Furthermore, the transcript classes can be distinguished from each other by their kinetics of appearance/disappearance in the cytoplasm: The first transcription of the pol gene is indicated by the predominant presence of class 2 and class 4 mRNAs at 2 hr postinfection (h.p.i.), followed by an increase of class 1 transcripts up to 4 h.p.i. and a parallel decrease of class 2 mRNAs. These data suggest that expression of the pol gene is finely regulated already at the transcriptional and/or posttranscriptional level prior to the translation of pol mRNAs. © 1991.
引用
收藏
页码:505 / 518
页数:14
相关论文
共 73 条
[1]   SIMIAN VIRUS-40 MAJOR LATE PROMOTER - A NOVEL TRIPARTITE STRUCTURE THAT INCLUDES INTRAGENIC SEQUENCES [J].
AYER, DE ;
DYNAN, WS .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2021-2033
[2]   DNA-SEQUENCE AND EXPRESSION OF THE B95-8 EPSTEIN-BARR VIRUS GENOME [J].
BAER, R ;
BANKIER, AT ;
BIGGIN, MD ;
DEININGER, PL ;
FARRELL, PJ ;
GIBSON, TJ ;
HATFULL, G ;
HUDSON, GS ;
SATCHWELL, SC ;
SEGUIN, C ;
TUFFNELL, PS ;
BARRELL, BG .
NATURE, 1984, 310 (5974) :207-211
[3]   DELETIONS COVERING THE PUTATIVE PROMOTER REGION OF EARLY MESSENGER-RNAS OF SIMIAN-VIRUS-40 DO NOT ABOLISH T-ANTIGEN EXPRESSION [J].
BENOIST, C ;
CHAMBON, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07) :3865-3869
[4]   SIZING AND MAPPING OF EARLY ADENOVIRUS MESSENGER-RNAS BY GEL-ELECTROPHORESIS OF S1 ENDONUCLEASE-DIGESTED HYBRIDS [J].
BERK, AJ ;
SHARP, PA .
CELL, 1977, 12 (03) :721-732
[5]  
BROACH JR, 1982, COLD SPRING HARB SYM, V45, P1165
[6]   GENETIC STUDIES WITH HERPES-SIMPLEX VIRUS TYPE-1 - ISOLATION OF TEMPERATURE-SENSITIVE MUTANTS, THEIR ARRANGEMENT INTO COMPLEMENTATION GROUPS AND RECOMBINATION ANALYSIS LEADING TO A LINKAGE MAP [J].
BROWN, SM ;
RITCHIE, DA ;
SUBAKSHA.JH .
JOURNAL OF GENERAL VIROLOGY, 1973, 18 (MAR) :329-346
[8]  
CHALLBERG MD, 1989, ANNU REV BIOCHEM, V58, P671
[9]   AN UNUSUAL SPLICED HERPES-SIMPLEX VIRUS TYPE-1 TRANSCRIPT WITH SEQUENCE HOMOLOGY TO EPSTEIN-BARR VIRUS-DNA [J].
COSTA, RH ;
DRAPER, KG ;
KELLY, TJ ;
WAGNER, EK .
JOURNAL OF VIROLOGY, 1985, 54 (02) :317-328
[10]   DIRECT DEMONSTRATION THAT THE ABUNDANT 6-KILOBASE HERPES-SIMPLEX VIRUS TYPE-1 MESSENGER-RNA MAPPING BETWEEN 0.23 AND 0.27 MAP UNITS ENCODES THE MAJOR CAPSID PROTEIN VP5 [J].
COSTA, RH ;
COHEN, G ;
EISENBERG, R ;
LONG, D ;
WAGNER, E .
JOURNAL OF VIROLOGY, 1984, 49 (01) :287-292