Literature DB >> 2475637

Identification and characterization of transcription termination sites in the Escherichia coli lacZ gene.

E C Ruteshouser1, J P Richardson.   

Abstract

The Escherichia coli lacZ gene contains a series of latent transcriptional terminators that are responsible for the polar effects of certain mutations. We demonstrate, using gel electrophoretic size analyses and nuclease S1 mapping procedures, that RNA polymerase terminates RNA synthesis in the vicinity of five positions 180, 220, 379, 421 and 463 base-pairs downstream from the start point during transcription of lacZ DNA in vitro in the presence of rho factor. Termination at all but the 421 position depends on rho factor. In the in vitro assays with 0.05 M-KCl and excess rho (36 nM), the terminators are moderately effective, having efficiencies that range from about 8% at the 180 base-pair site to 56% at the 463 base-pair site. These termination stop points correspond to five of the 11 transcriptional pause sites between 180 and 463 base-pairs. Several stop points also correspond to 3' end points of lacZ mRNA isolated from cells containing the strongly polar lacZ-U118 mutation and from cells starved for serine, thus confirming that these latent terminators are responsible for the polar effect and demonstrating that they also function under a condition of physiological stress that prevents the transcription from being translated properly. Two other potential termination factors, NusA protein and cyclic AMP receptor protein have no effect in vitro on the efficiency of termination at the five lacZ sites.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2475637     DOI: 10.1016/0022-2836(89)90085-5

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


  22 in total

1.  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

2.  Bacteriophage T7 RNA polymerase travels far ahead of ribosomes in vivo.

Authors:  I Iost; J Guillerez; M Dreyfus
Journal:  J Bacteriol       Date:  1992-01       Impact factor: 3.490

3.  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

4.  Expression of psbA genes produces prominent 5' psbA mRNA fragments in Synechococcus sp. PCC 7942.

Authors:  A J Soitamo; K Sippola; E M Aro
Journal:  Plant Mol Biol       Date:  1998-08       Impact factor: 4.076

5.  An rne-1 pnp-7 double mutation suppresses the temperature-sensitive defect of lacZ gene expression in a divE mutant.

Authors:  T Aiso; R Ohki
Journal:  J Bacteriol       Date:  1998-03       Impact factor: 3.490

6.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1989-11-25       Impact factor: 16.971

7.  Escherichia coli rho factor induces release of yeast RNA polymerase II but not polymerase I or III.

Authors:  W H Lang; T Platt; R H Reeder
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-28       Impact factor: 11.205

Review 8.  Tuning the sequence specificity of a transcription terminator.

Authors:  Michael R Lawson; James M Berger
Journal:  Curr Genet       Date:  2019-02-09       Impact factor: 3.886

9.  Entropy-based mechanism of ribosome-nucleoid segregation in E. coli cells.

Authors:  Jagannath Mondal; Benjamin P Bratton; Yijie Li; Arun Yethiraj; James C Weisshaar
Journal:  Biophys J       Date:  2011-06-08       Impact factor: 4.033

10.  Identification and characterization of the terminators of the lys and P transcripts of bacteriophage Mu.

Authors:  J Zha; Z Zhao; M M Howe
Journal:  J Bacteriol       Date:  1994-02       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.