A 100-KILODALTON POLYPEPTIDE ENCODED BY OPEN READING FRAME (ORF) 1B OF THE CORONAVIRUS INFECTIOUS-BRONCHITIS VIRUS IS PROCESSED BY ORF 1A PRODUCTS

被引:52
作者
LIU, DX
BRIERLEY, I
TIBBLES, KW
BROWN, TDK
机构
基金
英国医学研究理事会;
关键词
D O I
10.1128/JVI.68.9.5772-5780.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genome-length mRNA (mRNA 1) of the coronavirus infectious bronchitis virus (IBV) contains two large open reading frames (ORFs), 1a and 1b, with the potential to encode polypeptides of 441 and 300 kDa, respectively. The downstream ORF, ORF 1b, is expressed by a ribosomal frameshifting mechanism. In an effort to detect viral polypeptides encoded by ORF 1b in virus-infected cells, immunoprecipitations were carried out with a panel of region-specific antisera. A polypeptide of approximately 100 kDa was precipitated from IBV-infected, but not mock-infected Vero cells by one of these antisera (V58). Antiserum V58 was raised against a bacterially expressed fusion protein containing polypeptide sequences encoded by ORF 1b nucleotides 14492 to 15520; it recognizes specifically the corresponding in vitro-synthesized target protein. A polypeptide comigrating with the 100,000-molecular-weight protein (100K protein) identified in infected cells was also detected when the IBV sequence from nucleotides 8693 to 16980 was expressed in Vero cells by using a vaccinia virus-T7 expression system. Deletion analysis revealed that the sequence encoding the C terminus of the 100K polypeptide lies close to nucleotide 15120; it may therefore be generated by proteolysis at a potential QS cleavage site encoded by nucleotides 15129 to 15135. In contrast, expression of IBV sequences from nucleotides 10752 to 16980 generated two polypeptides of approximately 62 and 235 kDa, which represent the ORF 1a stop product and the 1a-1b fused product generated by a frameshifting mechanism, respectively, but no processed products were observed. Since the putative picornavirus 3C-like proteinase domain is located in ORF 1a between nucleotides 8937 and 9357, this observation suggests that deletion of the picornavirus 3C-like proteinase domain and surrounding regions abolishes processing of the 1b polyprotein. In addition, the in vitro translation and in vivo transfection studies also indicate that the ORF 1a region between nucleotides 8763 and 10720 contains elements that down-regulate the expression of ORF 1b.
引用
收藏
页码:5772 / 5780
页数:9
相关论文
共 30 条
[11]   INTRACELLULAR PROCESSING OF THE N-TERMINAL ORF-1A PROTEINS OF THE CORONAVIRUS MHV-A59 REQUIRES MULTIPLE PROTEOLYTIC EVENTS [J].
DENISON, MR ;
ZOLTICK, PW ;
HUGHES, SA ;
GIANGRECO, B ;
OLSON, AL ;
PERLMAN, S ;
LEIBOWITZ, JL ;
WEISS, SR .
VIROLOGY, 1992, 189 (01) :274-284
[12]   IDENTIFICATION OF POLYPEPTIDES ENCODED IN OPEN READING FRAME-1B OF THE PUTATIVE POLYMERASE GENE OF THE MURINE CORONAVIRUS MOUSE HEPATITIS VIRUS-A59 [J].
DENISON, MR ;
ZOLTICK, PW ;
LEIBOWITZ, JL ;
PACHUK, CJ ;
WEISS, SR .
JOURNAL OF VIROLOGY, 1991, 65 (06) :3076-3082
[13]   EUKARYOTIC TRANSIENT-EXPRESSION SYSTEM BASED ON RECOMBINANT VACCINIA VIRUS THAT SYNTHESIZES BACTERIOPHAGE-T7 RNA-POLYMERASE [J].
FUERST, TR ;
NILES, EG ;
STUDIER, FW ;
MOSS, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (21) :8122-8126
[14]   SEQUENCES THAT CONFER BETA-TUBULIN AUTOREGULATION THROUGH MODULATED MESSENGER-RNA STABILITY RESIDE WITHIN EXON-1 OF A BETA-TUBULIN MESSENGER-RNA [J].
GAY, DA ;
YEN, TJ ;
LAU, JTY ;
CLEVELAND, DW .
CELL, 1987, 50 (05) :671-679
[15]   CORONAVIRUS GENOME - PREDICTION OF PUTATIVE FUNCTIONAL DOMAINS IN THE NON-STRUCTURAL POLYPROTEIN BY COMPARATIVE AMINO-ACID SEQUENCE-ANALYSIS [J].
GORBALENYA, AE ;
KOONIN, EV ;
DONCHENKO, AP ;
BLINOV, VM .
NUCLEIC ACIDS RESEARCH, 1989, 17 (12) :4847-4861
[16]   NUCLEOTIDE-SEQUENCE OF THE HUMAN CORONAVIRUS 229E RNA-POLYMERASE LOCUS [J].
HEROLD, J ;
RAABE, T ;
SCHELLEPRINZ, B ;
SIDDELL, SG .
VIROLOGY, 1993, 195 (02) :680-691
[17]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[18]   THE COMPLETE SEQUENCE (22 KILOBASES) OF MURINE CORONAVIRUS GENE-1 ENCODING THE PUTATIVE PROTEASES AND RNA-POLYMERASE [J].
LEE, HJ ;
SHIEH, CK ;
GORBALENYA, AE ;
KOONIN, EV ;
LAMONICA, N ;
TULER, J ;
BAGDZHADZHYAN, A ;
LAI, MMC .
VIROLOGY, 1991, 180 (02) :567-582
[19]   IDENTIFICATION AND EXPRESSION OF THE HUMAN HERPESVIRUS-6 GLYCOPROTEIN-H AND INTERACTION WITH AN ACCESSORY 40K-GLYCOPROTEIN [J].
LIU, DX ;
GOMPELS, UA ;
NICHOLAS, J ;
LELLIOTT, C .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :1847-1857
[20]   A POLYCISTRONIC MESSENGER-RNA SPECIFIED BY THE CORONAVIRUS INFECTIOUS-BRONCHITIS VIRUS [J].
LIU, DX ;
CAVANAGH, D ;
GREEN, P ;
INGLIS, SC .
VIROLOGY, 1991, 184 (02) :531-544