Literature DB >> 6309406

Evidence that a nucleotide sequence, "boxA," is involved in the action of the NusA protein.

D I Friedman, E R Olson.   

Abstract

We report the isolation of a mutation, boxA1, in the nutR region of the phage lambda genome. The nutR region, located downstream of the pR promoter, includes the site nutR where the lambda N protein is thought to act to render subsequent transcription termination-resistant. We have previously suggested that the boxA sequence, 5'CGCTCTTA3' (or its RNA analog), located 8 bp promoter-proximal to nutR, might be the recognition site for the E. coli host factor, NusA, which has been shown to be necessary for N action. The boxA1 mutation, an A:T to T:A transversion, results in a changed boxA sequence upstream of nutR, CGCTCTTT. This change is necessary for lambda to effectively use the NusA of Salmonella typhimurium, a NusA function not normally active with the N product of lambda. Other lambdoid phages with unique N functions and nut sites that are normally active with the NusA of Salmonella have boxA sequences with the terminal three Ts. Moreover, sequences closely resembling boxA have been found near transcription termination sequences in E. coli operons where NusA has been shown to be involved in termination. These findings identify boxA as an important recognition signal for the NusA protein.

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Year:  1983        PMID: 6309406     DOI: 10.1016/0092-8674(83)90144-7

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


  43 in total

Review 1.  How the phage lambda N gene product suppresses transcription termination: communication of RNA polymerase with regulatory proteins mediated by signals in nascent RNA.

Authors:  A Das
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

2.  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

3.  Genetic interaction between the beta' subunit of RNA polymerase and the arginine-rich domain of Escherichia coli nusA protein.

Authors:  K Ito; K Egawa; Y Nakamura
Journal:  J Bacteriol       Date:  1991-02       Impact factor: 3.490

4.  Nucleotide sequence of the Escherichia coli recJ chromosomal region and construction of recJ-overexpression plasmids.

Authors:  S T Lovett; R D Kolodner
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

5.  Inhibition of transcription of cytosine-containing DNA in vitro by the alc gene product of bacteriophage T4.

Authors:  R H Drivdahl; E M Kutter
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

6.  Ribosomal protein L4 stimulates in vitro termination of transcription at a NusA-dependent terminator in the S10 operon leader.

Authors:  J M Zengel; L Lindahl
Journal:  Proc Natl Acad Sci U S A       Date:  1990-04       Impact factor: 11.205

7.  An RNA enhancer in a phage transcriptional antitermination complex functions as a structural switch.

Authors:  L Su; J T Radek; L A Labeots; K Hallenga; P Hermanto; H Chen; S Nakagawa; M Zhao; S Kates; M A Weiss
Journal:  Genes Dev       Date:  1997-09-01       Impact factor: 11.361

8.  Regulation of DNA superhelicity by rpoB mutations that suppress defective Rho-mediated transcription termination in Escherichia coli.

Authors:  G F Arnold; I Tessman
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

9.  Two-step cloning and expression in Escherichia coli of the DNA restriction-modification system StyLTI of Salmonella typhimurium.

Authors:  O De Backer; C Colson
Journal:  J Bacteriol       Date:  1991-02       Impact factor: 3.490

10.  RNA-binding specificity of E. coli NusA.

Authors:  Stefan Prasch; Marcel Jurk; Robert S Washburn; Max E Gottesman; Birgitta M Wöhrl; Paul Rösch
Journal:  Nucleic Acids Res       Date:  2009-06-10       Impact factor: 16.971

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