Literature DB >> 7460952

Demonstration of the early--late switch in vitro with bacteriophage T7 DNA as template.

E Fuchs, K P Hirth, B Henrich, G Kälberer.   

Abstract

A protein-synthesizing system in vitro, programmed with bacteriophage T7 DNA as template, changed the specificity of gene expression in the course of incubation as a result of newly synthesized T7 early proteins. The system mimics largely the situation in vivo on both the transcriptional and the translational levels, i.e. early gene expression is turned off shortly after late synthesis has been started. These results suggest that the switch from early to late expression does not necessarily require changes in the cellular environment nor is it dependent on the presence of membranes. The main part in this process is played by the phage-dependent RNA polymerase (gene 1 product), whose activity appears 8-10 min after start of incubation. When its activity is reduced by inhibitors or creation of non-optimal conditions, the system is not able to manage the early--late switch.

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Year:  1980        PMID: 7460952     DOI: 10.1111/j.1432-1033.1980.tb06139.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  2 in total

1.  More than 150 nucleotides flanking the initiation codon contribute to the efficiency of the ribosomal binding site from bacteriophage T7 gene 1.

Authors:  R M Geisen; H P Fatscher; E Fuchs
Journal:  Nucleic Acids Res       Date:  1987-06-25       Impact factor: 16.971

2.  An unstructured mRNA region and a 5' hairpin represent important elements of the E. coli translation initiation signal determined by using the bacteriophage T7 gene 1 translation start site.

Authors:  A Helke; R M Geisen; M Vollmer; M L Sprengart; E Fuchs
Journal:  Nucleic Acids Res       Date:  1993-12-11       Impact factor: 16.971

  2 in total

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