Literature DB >> 2511323

Codon contexts from weakly expressed genes reduce expression in vivo.

L S Folley1, M Yarus.   

Abstract

Nucleotides that neighbor codons in Escherichia coli genes are highly non-random. Furthermore, these context biases are stronger and extend farther from the codon in weakly expressed than in highly expressed genes. We therefore suggested that codon contexts are selected to reduce gene expression levels. We now compare the expression levels of lacZ genes containing two specific coding sequences (context inserts). One context insert represents contexts seen in weakly expressed genes (low variant); the other represents contexts seen in highly expressed genes (high variant). The two variants have identical nucleotide and codon compositions, and encode the same protein. A permutation of four nucleotides, which changes eight codon:codon interfaces of 1043, comprises the only difference between the high and low context variant genes. In three different lacZ mRNAs, the low variant was expressed at a level significantly below that of the high variant. This context effect depends entirely on translation of the contexts in the correct frame; its magnitude depends in part on the placement of other features (e.g. transcriptional pauses and terminators, or perhaps other slow codons or contexts) in the mRNAs. Changing the ribosome density on the message by changing the ribosome binding site distinguishes between dropoff, interference and polarity, three fundamentally different types of models for the context effect. The expression difference between context variants is eliminated by both increases and decreases in the ribosome initiation frequency, as uniquely predicted by the polarity model. In fact, data from all constructions are accommodated by a model in which slow translation of the low context insert increases rho-dependent transcriptional termination within the test gene. The data suggest that the rates of translational initiation and elongation are poised with respect to the rate of transcriptional elongation so that all are influential in setting the expression level of wild-type lacZ. We conclude that context-induced polarity will exist in genes wherever low and reproducible gene product levels have been selected.

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Year:  1989        PMID: 2511323     DOI: 10.1016/0022-2836(89)90003-x

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  23 in total

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Review 2.  Codon context.

Authors:  R H Buckingham
Journal:  Experientia       Date:  1990-12-01

3.  Transcription of single-copy hybrid lacZ genes by T7 RNA polymerase in Escherichia coli: mRNA synthesis and degradation can be uncoupled from translation.

Authors:  M Chevrier-Miller; N Jacques; O Raibaud; M Dreyfus
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

4.  A simple and sensitive in vivo luciferase assay for tRNA-mediated nonsense suppression.

Authors:  D W Schultz; M Yarus
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

5.  Attenuation of human respiratory syncytial virus by genome-scale codon-pair deoptimization.

Authors:  Cyril Le Nouën; Linda G Brock; Cindy Luongo; Thomas McCarty; Lijuan Yang; Masfique Mehedi; Eckard Wimmer; Steffen Mueller; Peter L Collins; Ursula J Buchholz; Joshua M DiNapoli
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-25       Impact factor: 11.205

6.  In the Escherichia coli lacZ gene the spacing between the translating ribosomes is insensitive to the efficiency of translation initiation.

Authors:  J Guillerez; M Gazeau; M Dreyfus
Journal:  Nucleic Acids Res       Date:  1991-12-25       Impact factor: 16.971

Review 7.  You're one in a googol: optimizing genes for protein expression.

Authors:  Mark Welch; Alan Villalobos; Claes Gustafsson; Jeremy Minshull
Journal:  J R Soc Interface       Date:  2009-03-11       Impact factor: 4.118

8.  Conservation of location of several specific inhibitory codon pairs in the Saccharomyces sensu stricto yeasts reveals translational selection.

Authors:  Dalia H Ghoneim; Xiaoju Zhang; Christina E Brule; David H Mathews; Elizabeth J Grayhack
Journal:  Nucleic Acids Res       Date:  2019-02-20       Impact factor: 16.971

9.  Decoding with the A:I wobble pair is inefficient.

Authors:  J F Curran
Journal:  Nucleic Acids Res       Date:  1995-02-25       Impact factor: 16.971

Review 10.  Understanding the contribution of synonymous mutations to human disease.

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Journal:  Nat Rev Genet       Date:  2011-08-31       Impact factor: 53.242

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