Literature DB >> 1834523

The nut site of bacteriophage lambda is made of RNA and is bound by transcription antitermination factors on the surface of RNA polymerase.

J R Nodwell1, J Greenblatt.   

Abstract

The boxA and boxB components of the lambda nut site are important for transcriptional antitermination by the phage N protein. We show here that boxA and boxB RNA in N-modified transcription complexes are inaccessible to ribonucleases and have altered sensitivity to dimethylsulfate. N and NusA suffice to weakly protect boxB, independently of boxA and other factors. However, efficient protection of the entire nut site from ribonucleases requires boxA and boxB, N, NusA, NusB, S10, and NusG. Mutations in RNA polymerase, which inhibit antitermination by N in vivo, disallow protection of the nut site during transcription in vitro; therefore, the surface of RNA polymerase must coordinate the formation of complexes containing the antitermination factors and nut site RNA.

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Year:  1991        PMID: 1834523     DOI: 10.1101/gad.5.11.2141

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  37 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.  Transcription frequency modulates the efficiency of an attenuator preceding the rpoBC RNA polymerase genes of Escherichia coli: possible autogenous control.

Authors:  K L Steward; T Linn
Journal:  Nucleic Acids Res       Date:  1992-09-25       Impact factor: 16.971

3.  A quantitative description of the binding states and in vitro function of antitermination protein N of bacteriophage lambda.

Authors:  Clarke R Conant; Marc R Van Gilst; Stephen E Weitzel; William A Rees; Peter H von Hippel
Journal:  J Mol Biol       Date:  2005-04-01       Impact factor: 5.469

Review 4.  A new look at bacteriophage lambda genetic networks.

Authors:  Donald L Court; Amos B Oppenheim; Sankar L Adhya
Journal:  J Bacteriol       Date:  2006-11-03       Impact factor: 3.490

5.  Transfer of Tat and release of TAR RNA during the activation of the human immunodeficiency virus type-1 transcription elongation complex.

Authors:  N J Keen; M J Churcher; J Karn
Journal:  EMBO J       Date:  1997-09-01       Impact factor: 11.598

6.  Structural and functional analysis of the E. coli NusB-S10 transcription antitermination complex.

Authors:  Xiao Luo; He-Hsuan Hsiao; Mikhail Bubunenko; Gert Weber; Donald L Court; Max E Gottesman; Henning Urlaub; Markus C Wahl
Journal:  Mol Cell       Date:  2008-12-26       Impact factor: 17.970

7.  The antitermination activity of bacteriophage lambda N protein is controlled by the kinetics of an RNA-looping-facilitated interaction with the transcription complex.

Authors:  Clarke R Conant; Jim P Goodarzi; Steven E Weitzel; Peter H von Hippel
Journal:  J Mol Biol       Date:  2008-05-13       Impact factor: 5.469

8.  Control of transcription processivity in phage lambda: Nus factors strengthen the termination-resistant state of RNA polymerase induced by N antiterminator.

Authors:  J DeVito; A Das
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-30       Impact factor: 11.205

9.  Specific binding of Escherichia coli ribosomal protein S1 to boxA transcriptional antiterminator RNA.

Authors:  J Mogridge; J Greenblatt
Journal:  J Bacteriol       Date:  1998-04       Impact factor: 3.490

10.  Human immunodeficiency virus type 1 transactivator protein, tat, stimulates transcriptional read-through of distal terminator sequences in vitro.

Authors:  M A Graeble; M J Churcher; A D Lowe; M J Gait; J Karn
Journal:  Proc Natl Acad Sci U S A       Date:  1993-07-01       Impact factor: 11.205

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