Minimal sequence and structural requirements of a subgenomic RNA promoter for turnip crinkle virus

被引:35
作者
Wang, J
Carpenter, CD
Simon, AE [1 ]
机构
[1] Univ Massachusetts, Dept Biochem & Mol Biol, Amherst, MA 01003 USA
[2] Univ Massachusetts, Mol & Cellular Biol Program, Amherst, MA 01003 USA
基金
美国国家科学基金会;
关键词
turnip crinkle virus; RNA replication; RNA-dependent RNA polymerase; subgenomic RNAs; plant RNA viruses;
D O I
10.1006/viro.1998.9538
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Infection of plants or protoplasts with turnip crinkle Virus (TCV) results in the synthesis of the genomic RNA and two subgenomic (sg) RNAs of 1.7 kb and 1.45 kb, respectively. Both of the sgRNA promoters were characterized previously and their secondary structures predicted by computer analysis [J. Wang and A. E. Simon (1997). Virology 232, 174-186]. Secondary structure-sensitive chemical and enzymatic probes have now been used to determine the structure of the promoter directing synthesis of the 1.45-kb sgRNA, namely the 1.45-kb sgRNA promoter, in solution. The newly obtained structure conforms with the previously predicted hairpin structure except for the hairpin base: four CG base pairs and a CA bulge are present instead of an A bulge. Studies of deletions within the 96-nucleotide (nt) 1.45-kb sgRNA promoter defined a minimal 30-nt core sequence as essential for promoter activity: a 21-nt hairpin and a 9-nt flanking single-stranded sequence. Mutational analysis in the stem section of the core promoter supported a role for the primary sequence and secondary structure in promoter activity. Sequence alterations in the flanking single-stranded region further suggest that the sequence CCCAUUA, encompassing the transcription start site, is required for efficient transcription of the 1.45-kb sgRNA by the TCV RNA-dependent RNA polymerase in vivo. (C) 1999 Academic Press.
引用
收藏
页码:327 / 336
页数:10
相关论文
共 40 条
[1]  
Adkins S, 1997, RNA, V3, P634
[2]  
Adkins S, 1998, RNA, V4, P455
[3]   MAPPING THE PROMOTER FOR SUBGENOMIC RNA-SYNTHESIS ON BEET NECROTIC YELLOW VEIN VIRUS RNA-3 [J].
BALMORI, E ;
GILMER, D ;
RICHARDS, K ;
GUILLEY, H ;
JONARD, G .
BIOCHIMIE, 1993, 75 (07) :517-521
[4]  
Bernal JJ, 1997, RNA, V3, P1052
[5]   MUTATIONAL ANALYSIS OF CIS-ACTING SEQUENCES AND GENE-FUNCTION IN RNA3 OF CUCUMBER MOSAIC-VIRUS [J].
BOCCARD, F ;
BAULCOMBE, D .
VIROLOGY, 1993, 193 (02) :563-578
[6]   In vivo repair of 3'-end deletions in a TCV satellite RNA may involve two abortive synthesis and priming events [J].
Carpenter, CD ;
Simon, AE .
VIROLOGY, 1996, 226 (02) :153-160
[7]   In vivo restoration of biologically active 3' ends of virus-associated RNAs by nonhomologous RNA recombination and replacement of a terminal motif [J].
Carpenter, CD ;
Simon, AE .
JOURNAL OF VIROLOGY, 1996, 70 (01) :478-486
[8]   Analysis of sequences and predicted structures required for viral satellite RNA accumulation by in vivo genetic selection [J].
Carpenter, CD ;
Simon, AE .
NUCLEIC ACIDS RESEARCH, 1998, 26 (10) :2426-2432
[9]   INVOLVEMENT OF A STEM-LOOP STRUCTURE IN THE LOCATION OF JUNCTION SITES IN VIRAL-RNA RECOMBINATION [J].
CARPENTER, CD ;
OH, JW ;
ZHANG, CX ;
SIMON, AE .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 245 (05) :608-622
[10]   THE GENOME STRUCTURE OF TURNIP CRINKLE VIRUS [J].
CARRINGTON, JC ;
HEATON, LA ;
ZUIDEMA, D ;
HILLMAN, BI ;
MORRIS, TJ .
VIROLOGY, 1989, 170 (01) :219-226