The role of the pseudoknot at the 3' end of turnip yellow mosaic virus RNA in minus-strand synthesis by the viral RNA-Dependent RNA polymerase

被引:33
作者
Deiman, BALM [1 ]
Kortlever, RM [1 ]
Pleij, CWA [1 ]
机构
[1] LEIDEN UNIV,LEIDEN INST CHEM,GORLAEUS LABS,NL-2300 RA LEIDEN,NETHERLANDS
关键词
D O I
10.1128/JVI.71.8.5990-5996.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The tRNA-like structure at the 3' end of turnip yellow mosaic virus (TYMV) RNA was studied in order to determine the role of this structure in the initiation of minus-strand synthesis in vitro. Deletions in the 5'-to 3' direction up to the pseudoknot structure did not result in a decrease of transcription efficiency. However, transcription efficiency was reduced twofold when a fragment of 21 nucleotides, comprising the 3'-terminal hairpin, was used as a template, tRNA(Phe) from yeast, Escherichia coli 5S rRNA, and the 3'-terminal 208 nucleotides of alfalfa mosaic virus RNA 3 could not be transcribed by the RNA-dependent RNA polymerase (RdRp) of TYMV. Various mutations in the sequences of loop regions L1 and L2 or of stem region S1 of the pseudoknot were tested to further investigate the importance of the pseudoknot structure. The results were compared with those obtained in an earlier study on aminoacylation with the same mutants tR, M. W. Mans, M. H. van Steeg, P. W. G. Verlaan, C. W. A. Pleij, and L. Bosch. J. Mol. Biol, 223:221-232: 1992). Mutants which still harbor a stable pseudoknot, as proven by probing its structure, have a transcription efficiency very close to that of the wild-type virus. Disruption of the pseudoknot structure, however, gives rise to a drop in transcription efficiency to about 50%, No indications of base-specific interactions between L1, L2, or S1 of the pseudoknot and the RdRp were found.
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页码:5990 / 5996
页数:7
相关论文
共 23 条
[1]   IN-VITRO TRANSCRIPTS OF TURNIP YELLOW MOSAIC-VIRUS ENCOMPASSING A LONG 3' EXTENSION OR PRODUCED FROM A FULL-LENGTH CDNA CLONE HARBORING A 2 KB-LONG PCR-AMPLIFIED SEGMENT ARE INFECTIOUS [J].
BOYER, JC ;
DRUGEON, G ;
SERON, K ;
MORCHDEVIGNES, MD ;
AGNES, F ;
HAENNI, AL .
RESEARCH IN VIROLOGY, 1993, 144 (05) :339-348
[2]   DELETIONS IN THE 3'-TERMINAL TRANSFER RNA-LIKE STRUCTURE OF BROME MOSAIC-VIRUS RNA DIFFERENTIALLY AFFECT AMINOACYLATION AND REPLICATION INVITRO [J].
BUJARSKI, JJ ;
DREHER, TW ;
HALL, TC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (17) :5636-5640
[3]   Efficient transcription obtained by a new procedure of the tRNA-like structure of turnip yellow mosaic virus by a template-dependent and specific viral RNA polymerase [J].
Deiman, BALM ;
Seron, K ;
Jaspars, EMJ ;
Pleij, CWA .
JOURNAL OF VIROLOGICAL METHODS, 1997, 64 (02) :181-195
[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]   Aminoacylation identity switch of turnip yellow mosaic virus RNA from valine to methionine results in an infectious virus [J].
Dreher, TW ;
Tsai, CH ;
Skuzeski, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12212-12216
[6]  
EUSKEN CBE, 1994, NUCLEIC ACIDS RES, V22, P1346
[7]   THE 3' PROMOTER REGION INVOLVED IN RNA-SYNTHESIS DIRECTED BY THE TURNIP YELLOW MOSAIC-VIRUS GENOME INVITRO [J].
GARGOURIBOUZID, R ;
DAVID, C ;
HAENNI, AL .
FEBS LETTERS, 1991, 294 (1-2) :56-58
[8]   Interplay of tRNA-like structures from plant viral RNAs with partners of the translation and replication machineries [J].
Giege, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12078-12081
[9]   INTERACTION OF TURNIP YELLOW MOSAIC-VIRUS VAL-RNA WITH EUKARYOTIC ELONGATION-FACTOR EF-1-ALPHA - SEARCH FOR A FUNCTION [J].
JOSHI, RL ;
RAVEL, JM ;
HAENNI, AL .
EMBO JOURNAL, 1986, 5 (06) :1143-1148
[10]   ELONGATION FACTOR VIRAL GENOME INTERACTION DEPENDENT ON AMINOACYLATION OF TYMV AND TMV RNAS [J].
LITVAK, S ;
TARRAGO, A ;
TARRAGOL.L ;
ALLENDE, JE .
NATURE-NEW BIOLOGY, 1973, 241 (107) :88-90