Release factor 2 frameshifting sites in different bacteria

被引:71
作者
Baranov, PV [1 ]
Gesteland, RF [1 ]
Atkins, JF [1 ]
机构
[1] Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA
关键词
D O I
10.1093/embo-reports/kvf065
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 mRNA encoding Escherichia coli polypeptide chain release factor 2 (RF2) has two partially overlapping reading frames. Synthesis of RF2 involves ribosomes shifting to the +1 reading frame at the end of the first open reading frame (ORF). Frameshifting serves an autoregulatory function. The RF2 gene sequences from the 86 additional bacterial species now available have been analyzed. Thirty percent of them have a single ORF and their expression does not require frameshifting. In the similar to70% that utilize frameshifting, the sequence cassette responsible for frameshifting is highly conserved. In the E. coli RF2 gene, an internal Shine-Dalgarno (SID) sequence just before the shift site was shown earlier to be important for frameshifting. Mutagenic data presented here show that the spacer region between the SID sequence and the shift site influences frameshifting, and possible mechanisms are discussed. Internal translation initiation occurs at the shift site, but any functional role is obscure.
引用
收藏
页码:373 / 377
页数:5
相关论文
共 28 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Overriding standard decoding:: Implications of recoding for ribosome function and enrichment of gene expression [J].
Atkins, JF ;
Baranov, PV ;
Fayet, O ;
Herr, AJ ;
Howard, MT ;
Ivanov, IP ;
Matsufuji, S ;
Miller, WA ;
Moore, B ;
Prère, MF ;
Willis, NM ;
Zhou, J ;
Gesteland, RF .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 2001, 66 :217-232
[3]   RECODE:: a database of frameshifting, bypassing and codon redefinition utilized for gene expression [J].
Baranov, PV ;
Gurvich, OL ;
Fayet, O ;
Prère, MF ;
Miller, WA ;
Gesteland, RF ;
Atkins, JF ;
Giddings, MC .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :264-267
[4]  
BARANOV PV, 2002, IN PRESS GENE
[5]   Structure of the C-terminal end of the nascent peptide influences translation termination [J].
Bjornsson, A ;
MottaguiTabar, S ;
Isaksson, LA .
EMBO JOURNAL, 1996, 15 (07) :1696-1704
[6]   EXPRESSION OF PEPTIDE-CHAIN RELEASE FACTOR-II REQUIRES HIGH-EFFICIENCY FRAMESHIFT [J].
CRAIGEN, WJ ;
CASKEY, CT .
NATURE, 1986, 322 (6076) :273-275
[7]   BACTERIAL PEPTIDE-CHAIN RELEASE FACTORS - CONSERVED PRIMARY STRUCTURE AND POSSIBLE FRAMESHIFT REGULATION OF RELEASE FACTOR-II [J].
CRAIGEN, WJ ;
COOK, RG ;
TATE, WP ;
CASKEY, CT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (11) :3616-3620
[8]   USE OF TRANSFER-RNA SUPPRESSORS TO PROBE REGULATION OF ESCHERICHIA-COLI RELEASE FACTOR-II [J].
CURRAN, JF ;
YARUS, M .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 203 (01) :75-83
[9]   Mutations which alter the elbow region of tRNA2Gly reduce T4 gene 60 translational bypassing efficiency [J].
Herr, AJ ;
Atkins, JF ;
Gesteland, RF .
EMBO JOURNAL, 1999, 18 (10) :2886-2896
[10]   Single amino acid substitution in prokaryote polypeptide release factor 2 permits it to terminate translation at all three stop codons [J].
Ito, K ;
Uno, M ;
Nakamura, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) :8165-8169