Enhancer-like properties of an RNA element that modulates tombusvirus RNA accumulation

被引:45
作者
Ray, D [1 ]
White, KA [1 ]
机构
[1] York Univ, Dept Biol, N York, ON M3J 1P3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
RNA structure; RNA synthesis; RNA polymerase; plus-strand RNA virus; plant virus; TBSV;
D O I
10.1006/viro.1999.9630
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Prototypical defective interfering (DI) RNAs of the plus-strand RNA virus tomato bushy stunt virus contain four noncontiguous segments (regions I-IV) derived from the viral genome. Region I corresponds to 5'-noncoding sequence, regions II and III are derived from internal positions, and region IV represents a 3'-terminal segment We analyzed the internally located region III in a prototypical DI RNA to understand better its role in DI RNA accumulation. Our results indicate that (1) region III is not essential for DI RNA accumulation, but molecules that lack it accumulate at significantly reduced levels (similar to 10-fold lower), (2) region III is able to function at different positions and in opposite orientations, (3) a single copy of region III is favored over multiple copies, (4) the stimulatory effect observed on DI RNA accumulation is not due to region III-mediated RNA stabilization, (5) DI RNAs lacking region III permit the efficient accumulation of head-to-tail dimers and are less effective at suppressing helper RNA accumulation, and (6) negative-strand accumulation is also significantly depressed for DI RNAs lacking region III. Collectively, these results support a role for region III as an enhancer-like element that facilitates DI RNA replication. A scanning-type mutagenesis strategy was used to define portions of region III important for its stimulatory effect on DI RNA accumulation. Interestingly, the results revealed several differences in the requirements for activity when region III was in the forward versus the reverse orientation. In the context of the viral genome, region III was found to be essential for biological activity. This latter finding defines a critical role for this element in the reproductive cycle of the virus, (C) 1999 Academic Press.
引用
收藏
页码:162 / 171
页数:10
相关论文
共 30 条
[1]   POLIOVIRUS RNA-SYNTHESIS UTILIZES AN RNP COMPLEX FORMED AROUND THE 5'-END OF VIRAL-RNA [J].
ANDINO, R ;
RIECKHOF, GE ;
ACHACOSO, PL ;
BALTIMORE, D .
EMBO JOURNAL, 1993, 12 (09) :3587-3598
[2]   HOST EFFECTS AND SEQUENCES ESSENTIAL FOR ACCUMULATION OF DEFECTIVE INTERFERING RNAS OF CUCUMBER NECROSIS AND TOMATO BUSHY STUNT TOMBUSVIRUSES [J].
CHANG, YC ;
BORJA, M ;
SCHOLTHOF, HB ;
JACKSON, AO ;
MORRIS, TJ .
VIROLOGY, 1995, 210 (01) :41-53
[3]   GENERATION OF DEFECTIVE INTERFERING RNA DIMERS OF CYMBIDIUM RINGSPOT TOMBUSVIRUS [J].
DALMAY, T ;
SZITTYA, G ;
BURGYAN, J .
VIROLOGY, 1995, 207 (02) :510-517
[4]   MUTATIONAL ANALYSIS OF THE SEQUENCE AND STRUCTURAL REQUIREMENTS IN BROME MOSAIC-VIRUS RNA FOR MINUS STRAND PROMOTER ACTIVITY [J].
DREHER, TW ;
HALL, TC .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 201 (01) :31-40
[5]   CHARACTERIZATION AND BIOLOGICAL-ACTIVITY OF DI RNA DIMERS FORMED DURING CUCUMBER NECROSIS VIRUS COINFECTIONS [J].
FINNEN, RL ;
ROCHON, DM .
VIROLOGY, 1995, 207 (01) :282-286
[6]  
Guan HC, 1997, RNA, V3, P1401
[7]   3' TERMINAL PUTATIVE STEM-LOOP STRUCTURE REQUIRED FOR THE ACCUMULATION OF CYMBIDIUM RINGSPOT VIRAL-RNA [J].
HAVELDA, Z ;
BURGYAN, J .
VIROLOGY, 1995, 214 (01) :269-272
[8]   LOCALIZATION OF CIS-ACTING SEQUENCES ESSENTIAL FOR CYMBIDIUM RINGSPOT TOMBUSVIRUS DEFECTIVE INTERFERING RNA REPLICATION [J].
HAVELDA, Z ;
DALMAY, T ;
BURGYAN, J .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :2311-2316
[9]   THE COMPLETE GENOME STRUCTURE AND SYNTHESIS OF INFECTIOUS RNA FROM CLONES OF TOMATO BUSHY STUNT VIRUS [J].
HEARNE, PQ ;
KNORR, DA ;
HILLMAN, BI ;
MORRIS, TJ .
VIROLOGY, 1990, 177 (01) :141-151
[10]   Common themes in the function of transcription and splicing enhancers [J].
Hertel, KJ ;
Lynch, KW ;
Maniatis, T .
CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (03) :350-357