Normal cellular replication of Sendai virus without the trans-frame, nonstructural V protein

被引:57
作者
Delenda, C [1 ]
Hausmann, S [1 ]
Garcin, D [1 ]
Kolakofsky, D [1 ]
机构
[1] UNIV GENEVA,SCH MED,CMU,DEPT GENET & MICROBIOL,CH-1211 GENEVA,SWITZERLAND
关键词
D O I
10.1006/viro.1996.8354
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Sendai virus V protein is a nonstructural trans-frame protein in which a highly conserved cys-rich Zn2+-binding domain is fused to the N-terminal half of the P protein via mRNA editing. Using a recently developed system in which infectious virus is recovered from cDNA, we have engineered a virus in which a translation stop codon was placed al the beginning of the V ORF. Translation of the V-stop mRNA yields a W-like protein, i.e., a protein composed of the N-terminal half of the P protein alone which is naturally expressed at low levels from the P gene. This V-minus but W-augmented virus was found to replicate normally in cell culture and embryonated chicken eggs. The Sendai virus V protein is thus an accessory protein, and the cys-rich Zn2+-binding domain is likely to function in a specialized role during virus propagation. (C) 1997 Academic Press.
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收藏
页码:55 / 62
页数:8
相关论文
共 41 条
[1]   THE PHOSPHOPROTEIN GENE OF A DOLPHIN MORBILLIVIRUS ISOLATE EXHIBITS GENOMIC VARIATION AT THE EDITING SITE [J].
BOLT, G ;
ALEXANDERSEN, S ;
BLIXENKRONEMOLLER, M .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :3051-3058
[2]   INTRACELLULAR PHOSPHORYLATION OF THE SENDAI VIRUS P-PROTEIN [J].
BYRAPPA, S ;
HENDRICKS, DD ;
PAN, YB ;
SEYER, JM ;
GUPTA, KC .
VIROLOGY, 1995, 208 (01) :408-413
[3]   Sendai virus P protein is constitutively phosphorylated at serine249: High phosphorylation potential of the P protein [J].
Byrappa, S ;
Pan, YB ;
Gupta, KC .
VIROLOGY, 1996, 216 (01) :228-234
[4]   The sendai paramyxovirus accessory C proteins inhibit viral genome amplification in a promoter-specific fashion [J].
Cadd, T ;
Garcin, D ;
Tapparel, C ;
Itoh, M ;
Homma, M ;
Roux, L ;
Curran, J ;
Kolakofsky, D .
JOURNAL OF VIROLOGY, 1996, 70 (08) :5067-5074
[5]   MEASLES-VIRUS EDITING PROVIDES AN ADDITIONAL CYSTEINE-RICH PROTEIN [J].
CATTANEO, R ;
KAELIN, K ;
BACZKO, K ;
BILLETER, MA .
CELL, 1989, 56 (05) :759-764
[6]   CHARACTERIZATION OF THE SENDAI VIRUS V-PROTEIN WITH AN ANTIPEPTIDE ANTISERUM [J].
CURRAN, J ;
DEMELO, M ;
MOYER, S ;
KOLAKOFSKY, D .
VIROLOGY, 1991, 184 (01) :108-116
[7]   SENDAI VIRUS P-GENE PRODUCES MULTIPLE PROTEINS FROM OVERLAPPING OPEN READING FRAMES [J].
CURRAN, J ;
KOLAKOFSKY, D .
ENZYME, 1990, 44 (1-4) :244-249
[8]   THE SENDAI VIRUS P-GENE EXPRESSES BOTH AN ESSENTIAL PROTEIN AND AN INHIBITOR OF RNA-SYNTHESIS BY SHUFFLING MODULES VIA MESSENGER-RNA EDITING [J].
CURRAN, J ;
BOECK, R ;
KOLAKOFSKY, D .
EMBO JOURNAL, 1991, 10 (10) :3079-3085
[9]   AN N-TERMINAL DOMAIN OF THE SENDAI PARAMYXOVIRUS P-PROTEIN ACTS AS A CHAPERONE FOR THE NP PROTEIN DURING THE NASCENT CHAIN ASSEMBLY STEP OF GENOME REPLICATION [J].
CURRAN, J ;
MARQ, JB ;
KOLAKOFSKY, D .
JOURNAL OF VIROLOGY, 1995, 69 (02) :849-855
[10]   Reexamination of the sendai virus P protein domains required for RNA synthesis: A possible supplemental role for the P protein [J].
Curran, J .
VIROLOGY, 1996, 221 (01) :130-140