Literature DB >> 3081264

Inefficient translation initiation causes premature transcription termination in the lacZ gene.

P Stanssens, E Remaut, W Fiers.   

Abstract

Expression plasmids containing the E. coli lacZ coding region preceded by a set of different ribosome-binding sites and put under transcriptional control of the leftward promoter of phage lambda (PL) were used to study the synthesis of lacZ mRNA. In a normal host the steady state level of full-length lacZ mRNA varied 100-fold with the different synthesis levels of beta-galactosidase, whereas in a host expressing the antitermination protein N of phage lambda, all vectors synthesized the same amount of full-length lacZ mRNA, while maintaining the differences in beta-galactosidase expression. We present evidence for a causal relationship between the rate of ribosome loading and the continuation of transcription across the lacZ gene. We suggest that extended spacing between the RNA polymerase and the elongating ribosome causes transcriptional polarity by increasing the extent of premature termination. The conditional character of the termination event can best be explained by invoking termination factor Rho.

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Year:  1986        PMID: 3081264     DOI: 10.1016/0092-8674(86)90837-8

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  48 in total

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

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

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5.  Features of the rho-dependent transcription termination polar element within the hisG cistron of Salmonella typhimurium.

Authors:  M S Ciampi; P Alifano; A G Nappo; C B Bruni; M S Carlomagno
Journal:  J Bacteriol       Date:  1989-08       Impact factor: 3.490

6.  The ompA 5' untranslated RNA segment functions in Escherichia coli as a growth-rate-regulated mRNA stabilizer whose activity is unrelated to translational efficiency.

Authors:  S A Emory; J G Belasco
Journal:  J Bacteriol       Date:  1990-08       Impact factor: 3.490

7.  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

8.  Polynucleotide phosphorylase hinders mRNA degradation upon ribosomal protein S1 overexpression in Escherichia coli.

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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

10.  Cis control of gene expression in E.coli by ribosome queuing at an inefficient translational stop signal.

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Journal:  EMBO J       Date:  2002-08-15       Impact factor: 11.598

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