Transcription map and expression of bovine herpesvirus-1 glycoprotein D in early region 4 of bovine adenovirus-3

被引:16
作者
Baxi, MK
Babiuk, LA
Mehtali, M
Tikoo, SK [1 ]
机构
[1] Univ Saskatchewan, Vet Infect Dis Org, Virol Grp, Saskatoon, SK S7N 5E3, Canada
[2] Transgene SA, Gene Therapy Dept, F-67000 Strasbourg, France
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1006/viro.1999.9826
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Early region 4 (E4) of bovine adenovirus type 3 (BAV-3) was analyzed by Northern blotting, RT-PCR analysis, cDNA sequencing, and S1 nuclease protection assays. The transcriptional map of the E4 region of BAV-3 has marked dissimilarities from those of mouse adenovirus-1, ovine adenovirus-287, and human adenovirus-2, for which the transcriptional maps have been constructed. The E4 region of BAV-3, located between 98.6 and 89.8 MU transcribes seven distinct classes of bovine adenovirus type 3 mRNA. The seven mRNA species formed by the removal of one to three introns share both the 3' end and a short 5' leader (25 nucleotides). The E4 mRNAs can encode at least five unique polypeptides, namely, 143R1, 69R, 143R2, 268R, and 219R. Isolation of a replication-competent recombinant "BAV404" containing 1.9-kb insertion [glycoprotein (gD) of bovine herpesvirus 1, under the control of a SV40 early promoter and poly(A)] in the region between E4 and the right ITR suggested that this region is nonessential for BAV-3 replication. Expression of go by BAV404 recombinant virus was confirmed by immunoprecipitation with go-specific monoclonal antibodies. Analysis of the kinetics of protein expression indicated that go is expressed at both early and late limes postinfection, These results suggest that: (a) 54 produces seven 5'-3' coterminal mRNAs and (b) the right terminal region of BAV-3 can be used for the expression of vaccine antigens. (C) 1999 Academic Press.
引用
收藏
页码:143 / 152
页数:10
相关论文
共 52 条
[1]  
Anderson WF, 1998, NATURE, V392, P25
[2]  
[Anonymous], ADENOVIRUS METHODS P
[3]   Effect of the E4 region on the persistence of transgene expression from adenovirus vectors [J].
Armentano, D ;
Zabner, J ;
Sacks, C ;
Sookdeo, CC ;
Smith, MP ;
StGeorge, JA ;
Wadsworth, SC ;
Smith, AE ;
Gregory, RJ .
JOURNAL OF VIROLOGY, 1997, 71 (03) :2408-2416
[4]   EARLY REGION-4 SEQUENCE AND BIOLOGICAL COMPARISON OF 2 ISOLATES OF MOUSE ADENOVIRUS TYPE-1 [J].
BALL, AO ;
BEARD, CW ;
VILLEGAS, P ;
SPINDLER, KR .
VIROLOGY, 1991, 180 (01) :257-265
[5]  
BARTHA A, 1969, ACTA VET ACAD SCI H, V19, P319
[6]   Characterization of bovine adenovirus type 3 early region 2B [J].
Baxi, MK ;
Reddy, PS ;
Zakhartchouk, AN ;
Idamakanti, N ;
Pyne, C ;
Babiuk, LA ;
Tikoo, SK .
VIRUS GENES, 1998, 16 (03) :313-316
[7]   A HETEROPLOID PERMANENT CELL-LINE ORIGINATING FROM EMBRYONIC CALF THYROID SUPPORTING THE REPLICATION OF ALL KNOWN BOVINE ADENOVIRUS SEROTYPES [J].
BENKO, M ;
BARTHA, A ;
MOSTL, K ;
BURKI, F .
VETERINARY MICROBIOLOGY, 1989, 19 (04) :317-324
[8]   REDUNDANT CONTROL OF ADENOVIRUS LATE GENE-EXPRESSION BY EARLY REGION-4 [J].
BRIDGE, E ;
KETNER, G .
JOURNAL OF VIROLOGY, 1989, 63 (02) :631-638
[9]   A gene transfer vector-cell line system for complete functional complementation of adenovirus early regions E1 and E4 [J].
Brough, DE ;
Lizonova, A ;
Hsu, C ;
Kulesa, VA ;
Kovesdi, I .
JOURNAL OF VIROLOGY, 1996, 70 (09) :6497-6501
[10]   HIGH-LEVEL EXPRESSION OF THE ENVELOPE GLYCOPROTEINS OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 IN PRESENCE OF REV GENE USING HELPER-INDEPENDENT ADENOVIRUS TYPE-7 RECOMBINANTS [J].
CHANDA, PK ;
NATUK, RJ ;
MASON, BB ;
BHAT, BM ;
GREENBERG, L ;
DHEER, SK ;
MOLNARKIMBER, KL ;
MIZUTANI, S ;
LUBECK, MD ;
DAVIS, AR ;
HUNG, PP .
VIROLOGY, 1990, 175 (02) :535-547