Literature DB >> 1681509

Codon choice and potential complementarity between mRNA downstream of the initiation codon and bases 1471-1480 in 16S ribosomal RNA affects expression of glnS.

M Faxén1, J Plumbridge, L A Isaksson.   

Abstract

A cis-acting expression mutation, GAG to GAA, in the third codon of the glnS gene is analyzed. Both codons code for glutamic acid but the mutation is known to increase gene expression by four fold. We show that the mutation has an effect only if it is located in the beginning of a gene but not if located internally. Data are presented that suggest that the reason for the increased expression by the mutation is the potential formation of one more base pair between the mRNA and 16S ribosomal RNA. Gene expression varies about 16 fold as the number of potential base pairs within the sequence 1471-1480 in 16S RNA increase from two to ten. We also give evidence that supports the idea that the presence of rare codons near the beginning of the mRNA can affect expression.

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Year:  1991        PMID: 1681509      PMCID: PMC328883          DOI: 10.1093/nar/19.19.5247

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  25 in total

1.  A translational enhancer derived from tobacco mosaic virus is functionally equivalent to a Shine-Dalgarno sequence.

Authors:  D R Gallie; C I Kado
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

2.  Characterization of cis-acting mutations which increase expression of a glnS-lacZ fusion in Escherichia coli.

Authors:  J Plumbridge; D Söll
Journal:  Mol Gen Genet       Date:  1989-03

3.  Rates of aminoacyl-tRNA selection at 29 sense codons in vivo.

Authors:  J F Curran; M Yarus
Journal:  J Mol Biol       Date:  1989-09-05       Impact factor: 5.469

4.  What constitutes the signal for the initiation of protein synthesis on Escherichia coli mRNAs?

Authors:  M Dreyfus
Journal:  J Mol Biol       Date:  1988-11-05       Impact factor: 5.469

5.  Chemical measurement of steady-state levels of ten aminoacyl-transfer ribonucleic acid synthetases in Escherichia coli.

Authors:  F C Neidhardt; P L Bloch; S Pedersen; S Reeh
Journal:  J Bacteriol       Date:  1977-01       Impact factor: 3.490

6.  Accuracy of in vivo aminoacylation requires proper balance of tRNA and aminoacyl-tRNA synthetase.

Authors:  R Swanson; P Hoben; M Sumner-Smith; H Uemura; L Watson; D Söll
Journal:  Science       Date:  1988-12-16       Impact factor: 47.728

7.  Tightly regulated tac promoter vectors useful for the expression of unfused and fused proteins in Escherichia coli.

Authors:  E Amann; B Ochs; K J Abel
Journal:  Gene       Date:  1988-09-30       Impact factor: 3.688

8.  A novel sequence element derived from bacteriophage T7 mRNA acts as an enhancer of translation of the lacZ gene in Escherichia coli.

Authors:  P O Olins; S H Rangwala
Journal:  J Biol Chem       Date:  1989-10-15       Impact factor: 5.157

9.  Translation rates of individual codons are not correlated with tRNA abundances or with frequencies of utilization in Escherichia coli.

Authors:  F Bonekamp; H Dalbøge; T Christensen; K F Jensen
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

10.  Structural basis for misaminoacylation by mutant E. coli glutaminyl-tRNA synthetase enzymes.

Authors:  J J Perona; R N Swanson; M A Rould; T A Steitz; D Söll
Journal:  Science       Date:  1989-12-01       Impact factor: 47.728

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  25 in total

1.  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

2.  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

3.  A codon window in mRNA downstream of the initiation codon where NGG codons give strongly reduced gene expression in Escherichia coli.

Authors:  Ernesto I Gonzalez de Valdivia; Leif A Isaksson
Journal:  Nucleic Acids Res       Date:  2004-09-30       Impact factor: 16.971

4.  Dynamic evolution of translation initiation mechanisms in prokaryotes.

Authors:  So Nakagawa; Yoshihito Niimura; Kin-ichiro Miura; Takashi Gojobori
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-22       Impact factor: 11.205

5.  Accumulation of a mRNA decay intermediate by ribosomal pausing at a stop codon.

Authors:  A Björnsson; L A Isaksson
Journal:  Nucleic Acids Res       Date:  1996-05-01       Impact factor: 16.971

6.  Downstream box-anti-downstream box interactions are dispensable for translation initiation of leaderless mRNAs.

Authors:  A Resch; K Tedin; A Gründling; A Mündlein; U Bläsi
Journal:  EMBO J       Date:  1996-09-02       Impact factor: 11.598

7.  Complementarity of the 16S rRNA penultimate stem with sequences downstream of the AUG destabilizes the plastid mRNAs.

Authors:  H Kuroda; P Maliga
Journal:  Nucleic Acids Res       Date:  2001-02-15       Impact factor: 16.971

Review 8.  Strategies for achieving high-level expression of genes in Escherichia coli.

Authors:  S C Makrides
Journal:  Microbiol Rev       Date:  1996-09

9.  Expression cloning of the nox, mdh and ldh genes from Thermus species encoding NADH oxidase, malate dehydrogenase and lactate dehydrogenase.

Authors:  H J Park; R Kreutzer
Journal:  Appl Microbiol Biotechnol       Date:  1994-01       Impact factor: 4.813

10.  Reduced synonymous substitution rate at the start of enterobacterial genes.

Authors:  A Eyre-Walker; M Bulmer
Journal:  Nucleic Acids Res       Date:  1993-09-25       Impact factor: 16.971

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