PSEUDOKNOT-DEPENDENT READ-THROUGH OF RETROVIRAL GAG TERMINATION CODONS - IMPORTANCE OF SEQUENCES IN THE SPACER AND LOOP-2

被引:60
作者
WILLS, NM [1 ]
GESTELAND, RF [1 ]
ATKINS, JF [1 ]
机构
[1] UNIV UTAH, DEPT HUMAN GENET, SALT LAKE CITY, UT 84112 USA
关键词
PSEUDOKNOT; READ-THROUGH; RECODING; RETROVIRUS;
D O I
10.1002/j.1460-2075.1994.tb06731.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
Retroviruses whose gag and pol genes are in the same reading frame depend upon similar to 5% read-through of the gag UAG termination codon to make the gag-pol polyprotein. For murine leukemia virus, this read-through is dependent on a pseudoknot located eight nucleotides 3' of the UAG. Other retroviruses whose gag and pol genes are in the same frame can potentially form similar pseudoknots 3' of their UAG codons. Beyond the similar secondary structures, there is strong sequence conservation in the spacer region and in loop 2 of the pseudoknots. The detrimental effects of substitutions of several of these conserved spacer and loop 2 nucleotides in the murine leukemia virus sequence show their importance for the read-through process. The importance of specific nucleotides in loop 2 of the pseudoknot contrasts with the flexibility of sequence in loop 2 of the most intensively studied frameshift-promoting pseudoknot which occurs in infectious bronchitis virus. Two nucleotides in loop 2 of the murine leukemia virus pseudoknot, which were shown to be important by mutagenic analysis, display hypersensitivity to the single-strand specific nuclease, S1. They are likely to be particularly accessible or are in an unusually reactive conformation.
引用
收藏
页码:4137 / 4144
页数:8
相关论文
共 37 条
[1]   RIBOSOME GYMNASTICS - DEGREE OF DIFFICULTY 9.5, STYLE 10.0 [J].
ATKINS, JF ;
WEISS, RB ;
GESTELAND, RF .
CELL, 1990, 62 (03) :413-423
[2]   FUNCTIONAL-CHARACTERIZATION OF THE EUKARYOTIC SECIS ELEMENTS WHICH DIRECT SELENOCYSTEINE INSERTION AT UGA CODONS [J].
BERRY, MJ ;
BANU, L ;
HARNEY, JW ;
LARSEN, PR .
EMBO JOURNAL, 1993, 12 (08) :3315-3322
[3]   SELENOPROTEIN SYNTHESIS - AN EXPANSION OF THE GENETIC-CODE [J].
BOCK, A ;
FORCHHAMMER, K ;
HEIDER, J ;
BARON, C .
TRENDS IN BIOCHEMICAL SCIENCES, 1991, 16 (12) :463-467
[4]   MUTATIONAL ANALYSIS OF THE RNA PSEUDOKNOT COMPONENT OF A CORONAVIRUS RIBOSOMAL FRAMESHIFTING SIGNAL [J].
BRIERLEY, I ;
ROLLEY, NJ ;
JENNER, AJ ;
INGLIS, SC .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 220 (04) :889-902
[5]   CHARACTERIZATION OF AN EFFICIENT CORONAVIRUS RIBOSOMAL FRAMESHIFTING SIGNAL - REQUIREMENT FOR AN RNA PSEUDOKNOT [J].
BRIERLEY, I ;
DIGARD, P ;
INGLIS, SC .
CELL, 1989, 57 (04) :537-547
[6]   INTRODUCTION OF UAG, UAA, AND UGA NONSENSE MUTATIONS AT A SPECIFIC SITE IN THE ESCHERICHIA-COLI CHLORAMPHENICOL ACETYLTRANSFERASE GENE - USE IN MEASUREMENT OF AMBER, OCHRE, AND OPAL SUPPRESSION IN MAMMALIAN-CELLS [J].
CAPONE, JP ;
SEDIVY, JM ;
SHARP, PA ;
RAJBHANDARY, UL .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (09) :3059-3067
[7]   AN RNA PSEUDOKNOT AND AN OPTIMAL HEPTAMERIC SHIFT SITE ARE REQUIRED FOR HIGHLY EFFICIENT RIBOSOMAL FRAMESHIFTING ON A RETROVIRAL MESSENGER-RNA [J].
CHAMORRO, M ;
PARKIN, N ;
VARMUS, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (02) :713-717
[8]   GENETIC ORGANIZATION OF GIBBON APE LEUKEMIA-VIRUS [J].
DELASSUS, S ;
SONIGO, P ;
WAINHOBSON, S .
VIROLOGY, 1989, 173 (01) :205-213
[9]   EXPRESSION OF THE GAG-POL FUSION PROTEIN OF MOLONEY MURINE LEUKEMIA-VIRUS WITHOUT GAG PROTEIN DOES NOT INDUCE VIRION FORMATION OR PROTEOLYTIC PROCESSING [J].
FELSENSTEIN, KM ;
GOFF, SP .
JOURNAL OF VIROLOGY, 1988, 62 (06) :2179-2182
[10]   MUTATIONAL ANALYSIS OF THE GAG-POL JUNCTION OF MOLONEY MURINE LEUKEMIA-VIRUS - REQUIREMENTS FOR EXPRESSION OF THE GAG-POL FUSION PROTEIN [J].
FELSENSTEIN, KM ;
GOFF, SP .
JOURNAL OF VIROLOGY, 1992, 66 (11) :6601-6608