IDENTIFICATION OF 2 NEW POLYPEPTIDES ENCODED BY MESSENGER RNA5 OF THE CORONAVIRUS INFECTIOUS-BRONCHITIS VIRUS

被引:28
作者
LIU, DX
INGLIS, SC
机构
[1] UNIV CAMBRIDGE,DEPT PATHOL,DIV VIROL,TENNIS COURT RD,CAMBRIDGE CB2 1QP,ENGLAND
[2] IMMUNOL LTD,CAMBRIDGE CB4 4GN,ENGLAND
关键词
D O I
10.1016/0042-6822(92)90094-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The second smallest subgenomic messenger RNA, mRNA5, of the coronavirus infectious bronchitis virus includes in its "5′ unique region" two separate open reading frames (5a and 5b), whose coding function has not so far been established, and thus it may represent a dicistronic messenger RNA. We report here that two polypeptides with the sizes expected for the 5a and 5b products can be synthesised by in vitro translation of a single artificial mRNA containing both the 5a and 5b ORFs. To establish whether these polypeptides represent genuine virus gene products, both the 5a and 5b coding sequences were expressed as bacterial fusion proteins, and these were used to raise monospecific antisera. Antisera raised against both the 5a and 5b-specific sequences recognized specifically proteins of the expected size in infectious bronchitis virus-infected chicken kidney and Vero cells, indicating that 5a and 5b do represent genuine virus genes, and suggesting that mRNA5 is indeed functionally dicistronic. © 1992.
引用
收藏
页码:342 / 347
页数:6
相关论文
共 32 条
[1]   MEASLES VIRUS-P GENE CODES FOR 2 PROTEINS [J].
BELLINI, WJ ;
ENGLUND, G ;
ROZENBLATT, S ;
ARNHEITER, H ;
RICHARDSON, CD .
JOURNAL OF VIROLOGY, 1985, 53 (03) :908-919
[2]   THE 2.2-KB E1B MESSENGER-RNA OF HUMAN AD12 AND AD5 CODES FOR 2 TUMOR-ANTIGENS STARTING AT DIFFERENT AUG TRIPLETS [J].
BOS, JL ;
POLDER, LJ ;
BERNARDS, R ;
SCHRIER, PI ;
VANDENELSEN, PJ ;
VANDEREB, AJ ;
VANORMONDT, H .
CELL, 1981, 27 (01) :121-131
[3]   COMPLETION OF THE SEQUENCE OF THE GENOME OF THE CORONAVIRUS AVIAN INFECTIOUS-BRONCHITIS VIRUS [J].
BOURSNELL, MEG ;
BROWN, TDK ;
FOULDS, IJ ;
GREEN, PF ;
TOMLEY, FM ;
BINNS, MM .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :57-77
[4]  
BOURSNELL MEG, 1984, GENE, V29, P87, DOI 10.1016/0378-1119(84)90169-0
[5]   AN EFFICIENT RIBOSOMAL FRAME-SHIFTING SIGNAL IN THE POLYMERASE-ENCODING REGION OF THE CORONAVIRUS IBV [J].
BRIERLEY, I ;
BOURSNELL, MEG ;
BINNS, MM ;
BILIMORIA, B ;
BLOK, VC ;
BROWN, TDK ;
INGLIS, SC .
EMBO JOURNAL, 1987, 6 (12) :3779-3785
[6]   CHARACTERIZATION OF AN EFFICIENT CORONAVIRUS RIBOSOMAL FRAMESHIFTING SIGNAL - REQUIREMENT FOR AN RNA PSEUDOKNOT [J].
BRIERLEY, I ;
DIGARD, P ;
INGLIS, SC .
CELL, 1989, 57 (04) :537-547
[7]  
BRIERLEY I, 1990, CORONAVIRUSES THEIR, V276, P175
[8]   INVITRO SYNTHESIS OF 2 POLYPEPTIDES FROM A NONSTRUCTURAL GENE OF CORONAVIRUS MOUSE HEPATITIS-VIRUS STRAIN A59 [J].
BUDZILOWICZ, CJ ;
WEISS, SR .
VIROLOGY, 1987, 157 (02) :509-515
[9]   RECOMMENDATIONS OF THE CORONAVIRUS STUDY-GROUP FOR THE NOMENCLATURE OF THE STRUCTURAL PROTEINS, MESSENGER-RNAS, AND GENES OF CORONAVIRUSES [J].
CAVANAGH, D ;
BRIAN, DA ;
ENJUANES, L ;
HOLMES, KV ;
LAI, MMC ;
LAUDE, H ;
SIDDELL, SG ;
SPAAN, W ;
TAGUCHI, F ;
TALBOT, PJ .
VIROLOGY, 1990, 176 (01) :306-307
[10]   SIMPLE, EFFICIENT INVITRO SYNTHESIS OF CAPPED RNA USEFUL FOR DIRECT EXPRESSION OF CLONED EUKARYOTIC GENES [J].
CONTRERAS, R ;
CHEROUTRE, H ;
DEGRAVE, W ;
FIERS, W .
NUCLEIC ACIDS RESEARCH, 1982, 10 (20) :6353-6362