Literature DB >> 8599950

The downstream box: an efficient and independent translation initiation signal in Escherichia coli.

M L Sprengart1, E Fuchs, A G Porter.   

Abstract

The downstream box (DB) was originally described as a translational enhancer of several Escherichia coli and bacteriophage mRNAs located just downstream of the initiation codon. Here, we introduced nucleotide substitutions into the DB and Shine-Dalgarno (SD) region of the highly active bacteriophage T7 gene 10 ribosome binding site (RBS) to examine the possibility that the DB has an independent and functionally important role. Eradication of the SD sequence in the absence of a DB abolished the translational activity of RBS fragments that were fused to a dihydrofolate reductase reporter gene. In contrast, an optimized DB at various positions downstream of the initiation codon promoted highly efficient protein synthesis despite the lack of a SD region. The DB was not functional when shifted upstream of the initiation codon to the position of the SD sequence. Nucleotides 1469-1483 of 16S rRNA ('anti-downstream box') are complementary to the DB, and optimizing this complementarity strongly enhanced translation in the absence and presence of a SD region. We propose that the stimulatory interaction between the DB and the anti-DB places the start codon in close contact with the decoding region of 16S rRNA, thereby mediating independent and efficient initiation of translation.

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Year:  1996        PMID: 8599950      PMCID: PMC449985     

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  60 in total

1.  Lambda repressor regulates the switch between PR and Prm promoters.

Authors:  A Walz; V Pirrotta; K Ineichen
Journal:  Nature       Date:  1976-08-19       Impact factor: 49.962

2.  Translational initiation on structured messengers. Another role for the Shine-Dalgarno interaction.

Authors:  M H de Smit; J van Duin
Journal:  J Mol Biol       Date:  1994-01-07       Impact factor: 5.469

3.  Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elements.

Authors:  J J Dunn; F W Studier
Journal:  J Mol Biol       Date:  1983-06-05       Impact factor: 5.469

4.  Characterization of translational initiation sites in E. coli.

Authors:  G D Stormo; T D Schneider; L M Gold
Journal:  Nucleic Acids Res       Date:  1982-05-11       Impact factor: 16.971

5.  The ribosome binding sites recognized by E. coli ribosomes have regions with signal character in both the leader and protein coding segments.

Authors:  G F Scherer; M D Walkinshaw; S Arnott; D J Morré
Journal:  Nucleic Acids Res       Date:  1980-09-11       Impact factor: 16.971

6.  Structure of ribosome-bound messenger RNA as revealed by enzymatic accessibility studies.

Authors:  C W Kang; C R Cantor
Journal:  J Mol Biol       Date:  1985-01-20       Impact factor: 5.469

7.  Bacteriophage P2 late promoters. II. Comparison of the four late promoter sequences.

Authors:  G E Christie; R Calendar
Journal:  J Mol Biol       Date:  1985-02-05       Impact factor: 5.469

8.  Increased expression of a cloned gene by local mutagenesis of its promoter and ribosome binding site.

Authors:  N Warburton; P G Boseley; A G Porter
Journal:  Nucleic Acids Res       Date:  1983-09-10       Impact factor: 16.971

9.  Sequences of the Escherichia coli dnaG primase gene and regulation of its expression.

Authors:  B L Smiley; J R Lupski; P S Svec; R McMacken; G N Godson
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

10.  Translational initiation frequency of atp genes from Escherichia coli: identification of an intercistronic sequence that enhances translation.

Authors:  J E McCarthy; H U Schairer; W Sebald
Journal:  EMBO J       Date:  1985-02       Impact factor: 11.598

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  53 in total

1.  Mutation analysis of the 5' untranslated region of the cold shock cspA mRNA of Escherichia coli.

Authors:  K Yamanaka; M Mitta; M Inouye
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

2.  Sequences downstream of the translation initiation codon are important determinants of translation efficiency in chloroplasts.

Authors:  H Kuroda; P Maliga
Journal:  Plant Physiol       Date:  2001-01       Impact factor: 8.340

3.  Low-temperature-induced DnaA protein synthesis does not change initiation mass in Escherichia coli K-12.

Authors:  T Atlung; F G Hansen
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

4.  A sequence downstream of the initiation codon is essential for cold shock induction of cspB of Escherichia coli.

Authors:  J P Etchegaray; M Inouye
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

5.  Enhancement of translation by the downstream box does not involve base pairing of mRNA with the penultimate stem sequence of 16S rRNA.

Authors:  M O'Connor; T Asai; C L Squires; A E Dahlberg
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

6.  CspA, CspB, and CspG, major cold shock proteins of Escherichia coli, are induced at low temperature under conditions that completely block protein synthesis.

Authors:  J P Etchegaray; M Inouye
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

7.  Translation during cold adaptation does not involve mRNA-rRNA base pairing through the downstream box.

Authors:  A La Teana; A Brandi; M O'Connor; S Freddi; C L Pon
Journal:  RNA       Date:  2000-10       Impact factor: 4.942

8.  Role of ribosome recycling factor (RRF) in translational coupling.

Authors:  Y Inokuchi; A Hirashima; Y Sekine; L Janosi; A Kaji
Journal:  EMBO J       Date:  2000-07-17       Impact factor: 11.598

9.  Protein S1 counteracts the inhibitory effect of the extended Shine-Dalgarno sequence on translation.

Authors:  Anastassia V Komarova; Ludmila S Tchufistova; Elena V Supina; Irina V Boni
Journal:  RNA       Date:  2002-09       Impact factor: 4.942

10.  Comparative analysis of the base biases at the gene terminal portions in seven eukaryote genomes.

Authors:  Yoshihito Niimura; Mahito Terabe; Takashi Gojobori; Kin-ichiro Miura
Journal:  Nucleic Acids Res       Date:  2003-09-01       Impact factor: 16.971

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