FORMATION OF A THERMODYNAMICALLY METASTABLE STRUCTURE CONTAINING HAIRPIN-II IS CRITICAL FOR INFECTIVITY OF POTATO SPINDLE TUBER VIROID RNA

被引:99
作者
LOSS, P
SCHMITZ, M
STEGER, G
RIESNER, D
机构
关键词
SITE-DIRECTED MUTAGENESIS; STABILITY CALCULATIONS; TEMPERATURE-GRADIENT GEL ELECTROPHORESIS; TRANSCRIPTION FACTOR BINDING;
D O I
10.1002/j.1460-2075.1991.tb08002.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The functional relevance of a hairpin II-containing structure of viroid RNA was studied by site-directed mutagenesis, thermodynamic calculations, experimental denaturation curves and infectivity tests. Hairpin II is formed during thermal denaturation of circular viroids or as part of a metastable structure during synthesis of viroid replication intermediates. In potato spindle tuber viroid (PSTVd), eight single-site mutations were generated in the segments which form hairpin II. From the mutated viroid cDNA clones, linear RNA transcripts of PSTVd unit length were synthesized. The relevance of hairpin II for the mechanism of denaturation was confirmed quantitatively by optical denaturation curves and temperature-gradient gel electrophoresis. Infectivity tests showed that the mutations in the core region of hairpin II reverted to the wild type sequence whereas the mutations in the peripheral regions of hairpin II remained genetically stable. These data are in accordance with the natural variance of hairpin II in other viroids of the PSTVd class. Thus, the integrity of the core of hairpin II is critical for infectivity. Hairpin II exhibits a strong similarity in sequence as well as in three-dimensional structure to certain DNA GC-clusters found in the 5'-upstream regions of some genes in man, animals, viruses and plants. A hypothesis about a function of hairpin II as a binding site for host cell transcription factors is proposed.
引用
收藏
页码:719 / 727
页数:9
相关论文
共 51 条
[1]   AN RNA-POLYMERASE MUTANT WITH REDUCED ACCURACY OF CHAIN ELONGATION [J].
BLANK, A ;
GALLANT, JA ;
BURGESS, RR ;
LOEB, LA .
BIOCHEMISTRY, 1986, 25 (20) :5920-5928
[2]   LARGE-SCALE PURIFICATION OF VIROID RNA USING CS2SO4 GRADIENT CENTRIFUGATION AND HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
COLPAN, M ;
SCHUMACHER, J ;
BRUGGEMANN, W ;
SANGER, HL ;
RIESNER, D .
ANALYTICAL BIOCHEMISTRY, 1983, 131 (01) :257-265
[3]   CONSTRUCTION OF INFECTIOUS POTATO SPINDLE TUBER VIROID CDNA CLONES [J].
CRESS, DE ;
KIEFER, MC ;
OWENS, RA .
NUCLEIC ACIDS RESEARCH, 1983, 11 (19) :6821-6835
[4]   OLIGONUCLEOTIDE-DIRECTED MUTAGENESIS AS A GENERAL AND POWERFUL METHOD FOR STUDIES OF PROTEIN FUNCTION [J].
DALBADIEMCFARLAND, G ;
COHEN, LW ;
RIGGS, AD ;
MORIN, C ;
ITAKURA, K ;
RICHARDS, JH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (21) :6409-6413
[5]  
Diener T.O., 1987, VIROIDS
[7]  
DIENER TO, 1979, VIROIDS VIROID DISEA
[8]   STRUCTURE AND ELICITOR OR UV-LIGHT-STIMULATED EXPRESSION OF 2 4-COUMARATE-COA LIGASE GENES IN PARSLEY [J].
DOUGLAS, C ;
HOFFMANN, H ;
SCHULZ, W ;
HAHLBROCK, K .
EMBO JOURNAL, 1987, 6 (05) :1189-1195
[9]   TERTIARY STRUCTURE IN TRANSFER RIBONUCLEIC ACIDS [J].
FRESCO, JR ;
ADAMS, A ;
ASCIONE, R ;
HENLEY, D ;
LINDAHL, T .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1966, 31 :527-&
[10]   MULTIPLE SPECIFIC CONTACTS BETWEEN A MAMMALIAN TRANSCRIPTION FACTOR AND ITS COGNATE PROMOTERS [J].
GIDONI, D ;
DYNAN, WS ;
TJIAN, R .
NATURE, 1984, 312 (5993) :409-413