Programmed translational frameshifting

被引:286
作者
Farabaugh, PJ
机构
关键词
D O I
10.1128/MMBR.60.1.103-134.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Translating ribosomes maintain their reading flame with extreme accuracy. However, certain RNA sequences program the ribosome to alter the reading frame efficiently to allow for the expression of alternative translational products. Sites which cause the ribosome to shift frames, termed programmed frameshift sites occur in organisms from bacteria to higher eukaryotes. Mechanistically, the frameshift events are very diverse. Ribosomes may shift frames 1 base in the leftward, or -1, direction, 1 base in the rightward, or +1, direction, and even over dozens of nucleotides in the rightward direction an event termed a translational hop. By studying the sequence requirements of such sites, the primary, sequence of the peptides produced, and the effect of site-specific mutations researchers have defined the rules of programmed frameshifting at a large number of sites of all three types. Although the detailed mechanisms differ, the sites all conform to a general pattern. Programmed frameshifting occurs when the ribosome transiently pauses during elongation with a sequence in the decoding sites of the ribosome which predisposes it to shift frames. In almost all cases, this predisposition results from the ability of tRNAs to reposition themselves on cognate or near-cognate codons in the new reading frame. However this is not a universal requirement, since at least two programmed +1 frameshifts probably occur without tRNA slippage. These events occur when the mRNA sequence of the frameshift site manipulates the frame maintenance mechanism of the ribosome to increase drastically the probability of frame disruption. They may therefore be used as tools to probe this mechanism.
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页码:103 / +
页数:1
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共 230 条
[1]  
Atkins J. F., 1995, P471
[2]   LOW ACTIVITY OF BETA-GALACTOSIDASE IN FRAMESHIFT MUTANTS OF ESCHERICHIA-COLI [J].
ATKINS, JF ;
ELSEVIERS, D ;
GORINI, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (05) :1192-+
[3]   NORMAL TRANSFER-RNAS PROMOTE RIBOSOMAL FRAMESHIFTING [J].
ATKINS, JF ;
GESTELAND, RF ;
REID, BR ;
ANDERSON, CW .
CELL, 1979, 18 (04) :1119-1131
[4]  
ATKINS JF, 1975, J BIOL CHEM, V250, P5688
[5]   THE CONTEXT EFFECT DOES NOT REQUIRE A 4TH BASE PAIR [J].
AYER, D ;
YARUS, M .
SCIENCE, 1986, 231 (4736) :393-395
[6]   SPE1 AND SPE2 - 2 ESSENTIAL GENES IN THE BIOSYNTHESIS OF POLYAMINES THAT MODULATE +1-RIBOSOMAL FRAMESHIFTING IN SACCHAROMYCES-CEREVISIAE [J].
BALASUNDARAM, D ;
DINMAN, JD ;
TABOR, CW ;
TABOR, H .
JOURNAL OF BACTERIOLOGY, 1994, 176 (22) :7126-7128
[7]   SPERMIDINE DEFICIENCY INCREASES +1 RIBOSOMAL FRAMESHIFTING EFFICIENCY AND INHIBITS TY1 RETROTRANSPOSITION IN SACCHAROMYCES-CEREVISIAE [J].
BALASUNDARAM, D ;
DINMAN, JD ;
WICKNER, RB ;
TABOR, CW ;
TABOR, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :172-176
[8]   LOCALIZATION OF THE TARGET SITE FOR TRANSLATIONAL REGULATION OF THE L11-OPERON AND DIRECT EVIDENCE FOR TRANSLATIONAL COUPLING IN ESCHERICHIA-COLI [J].
BAUGHMAN, G ;
NOMURA, M .
CELL, 1983, 34 (03) :979-988
[9]   RIBOSOMAL FRAMESHIFTING IN THE YEAST RETROTRANSPOSON TY - TRANSFER-RNAS INDUCE SLIPPAGE ON A 7-NUCLEOTIDE MINIMAL SITE [J].
BELCOURT, MF ;
FARABAUGH, PJ .
CELL, 1990, 62 (02) :339-352
[10]   FRAMESHIFTING IN THE EXPRESSION OF THE ESCHERICHIA-COLI TRPR GENE OCCURS BY THE BYPASSING OF A SEGMENT OF ITS CODING SEQUENCE [J].
BENHAR, I ;
ENGELBERGKULKA, H .
CELL, 1993, 72 (01) :121-130