SUBGENOMIC RNAS OF LELYSTAD VIRUS CONTAIN A CONSERVED LEADER BODY JUNCTION SEQUENCE

被引:111
作者
MEULENBERG, JJM
DEMEIJER, EJ
MOORMANN, RJM
机构
[1] Central Veterinary Institute, Department of Virology, 8221 RA Lelystad
关键词
D O I
10.1099/0022-1317-74-8-1697
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
During the replication of Lelystad virus in alveolar lung macrophages, a 3'-coterminal nested set of six subgenomic RNAs (RNA2 to RNA7) is formed. These contain a common leader sequence derived from the 5' non-coding region of the genomic RNA. In this study, the sequence of the junction sites. i.e. the sites where the leader sequence joins to the body of the subgenomic RNA, was determined for all six subgenomic RNAs. For each subgenomic RNA, six to nine cDNA clones were isolated by means of reverse transcription and PCR. The nucleotide sequence at the junction site was identical for all eight cDNA clones derived from subgenomic RNA4. However, heterogeneity was observed in the nucleotide sequence surrounding the junction sites of the cDNA clones derived from subgenomic RNAs 2, 3, 5, 6 and 7. This heterogeneity suggests that the fusion of the leader to the body of the subgenomic RNA may be imprecise. The junction sites of the six subgenomic RNAs had a conserved sequence motif of six nucleotides (UCAACC or a highly similar sequence). The distance between the junction site and the translation initiation codon of the downstream open reading frame varied from nine to 83 nucleotides.
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页码:1697 / 1701
页数:5
相关论文
共 17 条
[1]   AN IN VITRO SYSTEM FOR THE LEADER-PRIMED TRANSCRIPTION OF CORONAVIRUS MRNAS [J].
BAKER, SC ;
LAI, MMC .
EMBO JOURNAL, 1990, 9 (12) :4173-4179
[2]   CHARACTERIZATION OF REPLICATIVE INTERMEDIATE RNA OF MOUSE HEPATITIS-VIRUS - PRESENCE OF LEADER RNA SEQUENCES ON NASCENT CHAINS [J].
BARIC, RS ;
STOHLMAN, SA ;
LAI, MMC .
JOURNAL OF VIROLOGY, 1983, 48 (03) :633-640
[3]   CHARACTERIZATION OF LEADER-RELATED SMALL RNAS IN CORONAVIRUS-INFECTED CELLS - FURTHER EVIDENCE FOR LEADER-PRIMED MECHANISM OF TRANSCRIPTION [J].
BARIC, RS ;
STOHLMAN, SA ;
RAZAVI, MK ;
LAI, MMC .
VIRUS RESEARCH, 1985, 3 (01) :19-33
[4]   SELF-SPLICING OF GROUP-I INTRONS [J].
CECH, TR .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :543-568
[5]   SEQUENCES OF 3' END OF GENOME AND OF 5' END OF OPEN READING FRAME 1A OF LACTATE DEHYDROGENASE-ELEVATING VIRUS AND COMMON JUNCTION MOTIFS BETWEEN 5' LEADER AND BODIES OF 7 SUBGENOMIC MESSENGER-RNAS [J].
CHEN, ZY ;
KUO, L ;
ROWLAND, RRR ;
EVEN, C ;
FAABERG, KS ;
PLAGEMANN, PGW .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :643-660
[6]   ALL SUBGENOMIC MESSENGER-RNAS OF EQUINE ARTERITIS VIRUS CONTAIN A COMMON LEADER SEQUENCE [J].
DEVRIES, AAF ;
CHIRNSIDE, ED ;
BREDENBEEK, PJ ;
GRAVESTEIN, LA ;
HORZINEK, MC ;
SPAAN, WJM .
NUCLEIC ACIDS RESEARCH, 1990, 18 (11) :3241-3247
[7]  
KUO L, 1992, VIRUS RES, V23, P55
[8]   DISCONTINUOUS TRANSCRIPTION GENERATES HETEROGENEITY AT THE LEADER FUSION SITES OF CORONAVIRUS MESSENGER-RNAS [J].
MAKINO, S ;
SOE, LH ;
SHIEH, CK ;
LAI, MMC .
JOURNAL OF VIROLOGY, 1988, 62 (10) :3870-3873
[9]   A SYSTEM FOR STUDY OF CORONAVIRUS MESSENGER-RNA SYNTHESIS - A REGULATED, EXPRESSED SUBGENOMIC DEFECTIVE INTERFERING RNA RESULTS FROM INTERGENIC SITE INSERTION [J].
MAKINO, S ;
JOO, M ;
MAKINO, JK .
JOURNAL OF VIROLOGY, 1991, 65 (11) :6031-6041
[10]  
MAKINO S, 1986, P NATL ACAD SCI USA, V83, P4202