Nucleotide sequence and genomic organization of Acyrthosiphon pisum virus

被引:49
作者
vanderWilk, F
Dullemans, AM
Verbeek, M
VandenHeuvel, JFJM
机构
[1] Department of Virology, DLO Res. Inst. for Plant P., 6700 GW Wageningen
关键词
D O I
10.1006/viro.1997.8835
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The nucleotide sequence of the genomic RNA of Acyrthosiphon pisum virus was determined. The APV genome is 10,016 nucleotides in length, excluding the 3'-end poly(A) track, and contains two large open reading frames (ORFs), encoding proteins of 296,340 and 63,279 Da. The ORF1 is preceded by an untranslated leader sequence of 267 nucleotides. The ORF1 product contains sequence motifs characteristic of RNA-dependent RNA polymerases, chymotrypsin-like proteases, and helicases. Interviral sequence comparison revealed significant similarities with viruses belonging to the so-called picornavirus superfamily. The ORF2 is most likely expressed by a -1 translational frameshift and is followed by an untranslated sequence of 222 nucleotides. Internal amino acid sequences of three capsid proteins (66K, 34K, 23/24K) were determined. Comparison of the obtained amino acid sequences with the APV sequence disclosed that the structural proteins are located in the 3'-terminal half of the genome. The 34K protein is encoded by the ORF1, while the 66K protein contains both ORF1-(34K) and ORF2-derived sequences and is probably expressed by a translational frameshift The 23/24K proteins mast likely arise by proteolytic breakdown of the 34K protein. Although the deduced APV genomic organization in some aspects resembles that of the picornaviruses, its overall genomic organization indicates that APV is a distinct species only distantly related to the Picornaviridae. (C) 1997 Academic Press.
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页码:353 / 362
页数:10
相关论文
共 32 条
[1]   PURIFICATION, CHARACTERIZATION, AND SOME PROPERTIES OF A VIRUS FROM THE APHID SITOBION-AVENAE [J].
ALLEN, MF ;
BALL, BV .
JOURNAL OF INVERTEBRATE PATHOLOGY, 1990, 55 (02) :162-168
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]   COMPARATIVE-ANALYSIS OF VIRAL CYSTEINE PROTEASE STRUCTURAL MODELS [J].
BAZAN, JF ;
FLETTERICK, RJ .
FEBS LETTERS, 1989, 249 (01) :5-7
[4]   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
[5]  
Cauchi MR, 1996, J MED VIROL, V49, P70
[6]   CLONED DNA COPIES OF COWPEA SEVERE MOSAIC-VIRUS GENOMIC RNAS - INFECTIOUS TRANSCRIPTS AND COMPLETE NUCLEOTIDE-SEQUENCE OF RNA-1 [J].
CHEN, XJ ;
BRUENING, G .
VIROLOGY, 1992, 191 (02) :607-618
[7]   The molecular biology of caliciviruses [J].
Clarke, IN ;
Lambden, PR .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :291-301
[8]   PURIFICATION AND CHARACTERIZATION OF A VIRUS FROM THE APHID RHOPALOSIPHUM-PADI [J].
DARCY, CJ ;
BURNETT, PA ;
HEWINGS, AD ;
GOODMAN, RM .
VIROLOGY, 1981, 112 (01) :346-349
[9]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[10]   CYSTEINE PROTEASES OF POSITIVE STRAND RNA VIRUSES AND CHYMOTRYPSIN-LIKE SERINE PROTEASES - A DISTINCT PROTEIN SUPERFAMILY WITH A COMMON STRUCTURAL FOLD [J].
GORBALENYA, AE ;
DONCHENKO, AP ;
BLINOV, VM ;
KOONIN, EV .
FEBS LETTERS, 1989, 243 (02) :103-114