Literature DB >> 8134358

RNA polymerase binding using a strongly acidic hydrophobic-repeat region of sigma 54.

Y Tintut1, C Wong, Y Jiang, M Hsieh, J D Gralla.   

Abstract

sigma 54 is a rare bacterial protein that substitutes for sigma 70 in the case of Escherichia coli genes transcribed by certain activators with enhancer protein-like properties. It contains a strongly acidic region of previously unknown function. Gel mobility-shift assays using sigma 54 deletion mutants show that this region is essential for sigma 54 to bind the core RNA polymerase and recruit it to the promoter. Multiple-point mutational analysis shows that the acidic amino acids and overlapping periodic hydrophobic amino acids are necessary for this binding. Related sequences are not found within the core binding determinant of sigma 70, which binds the same core RNA polymerase. This comparison suggests that the core RNA polymerase interacts differently with the two sigma factors, likely contributing to the critical differences in transcription mechanism in the two cases.

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Year:  1994        PMID: 8134358      PMCID: PMC43321          DOI: 10.1073/pnas.91.6.2120

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  33 in total

Review 1.  Transcriptional regulation in mammalian cells by sequence-specific DNA binding proteins.

Authors:  P J Mitchell; R Tjian
Journal:  Science       Date:  1989-07-28       Impact factor: 47.728

2.  Function of a bacterial activator protein that binds to transcriptional enhancers.

Authors:  D L Popham; D Szeto; J Keener; S Kustu
Journal:  Science       Date:  1989-02-03       Impact factor: 47.728

3.  Initiation of transcription at the bacterial glnAp2 promoter by purified E. coli components is facilitated by enhancers.

Authors:  A J Ninfa; L J Reitzer; B Magasanik
Journal:  Cell       Date:  1987-09-25       Impact factor: 41.582

4.  Structural and functional characterization of the short acidic transcriptional activation region of yeast GCN4 protein.

Authors:  I A Hope; S Mahadevan; K Struhl
Journal:  Nature       Date:  1988-06-16       Impact factor: 49.962

5.  Probing the Escherichia coli glnALG upstream activation mechanism in vivo.

Authors:  S Sasse-Dwight; J D Gralla
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

6.  Five intermediate complexes in transcription initiation by RNA polymerase II.

Authors:  S Buratowski; S Hahn; L Guarente; P A Sharp
Journal:  Cell       Date:  1989-02-24       Impact factor: 41.582

7.  Mutations that create new promoters suppress the sigma 54 dependence of glnA transcription in Escherichia coli.

Authors:  L J Reitzer; R Bueno; W D Cheng; S A Abrams; D M Rothstein; T P Hunt; B Tyler; B Magasanik
Journal:  J Bacteriol       Date:  1987-09       Impact factor: 3.490

8.  The nucleotide sequence of the sigma factor gene ntrA (rpoN) of Azotobacter vinelandii: analysis of conserved sequences in NtrA proteins.

Authors:  M Merrick; J Gibbins; A Toukdarian
Journal:  Mol Gen Genet       Date:  1987-12

9.  Klebsiella pneumoniae nifA product activates the Rhizobium meliloti nitrogenase promoter.

Authors:  V Sundaresan; J D Jones; D W Ow; F M Ausubel
Journal:  Nature       Date:  1983-02-24       Impact factor: 49.962

10.  Transcription of glnA in E. coli is stimulated by activator bound to sites far from the promoter.

Authors:  L J Reitzer; B Magasanik
Journal:  Cell       Date:  1986-06-20       Impact factor: 41.582

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  16 in total

1.  Single amino acid substitution mutants of Klebsiella pneumoniae sigma(54) defective in transcription.

Authors:  M Pitt; M T Gallegos; M Buck
Journal:  Nucleic Acids Res       Date:  2000-11-15       Impact factor: 16.971

Review 2.  The bacterial enhancer-dependent sigma(54) (sigma(N)) transcription factor.

Authors:  M Buck; M T Gallegos; D J Studholme; Y Guo; J D Gralla
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

3.  The role of region II in the RNA polymerase sigma factor sigma(N) (sigma(54)).

Authors:  E Southern; M Merrick
Journal:  Nucleic Acids Res       Date:  2000-07-01       Impact factor: 16.971

4.  Roles of genes 44, 50, and 51 in regulating gene expression and host takeover during infection of Bacillus subtilis by bacteriophage SPO1.

Authors:  Aruna Sampath; Charles R Stewart
Journal:  J Bacteriol       Date:  2004-03       Impact factor: 3.490

5.  PCR mutagenesis identifies a polymerase-binding sequence of sigma 54 that includes a sigma 70 homology region.

Authors:  Y Tintut; J D Gralla
Journal:  J Bacteriol       Date:  1995-10       Impact factor: 3.490

6.  Identification of an N-terminal region of sigma 54 required for enhancer responsiveness.

Authors:  A Syed; J D Gralla
Journal:  J Bacteriol       Date:  1998-11       Impact factor: 3.490

7.  Regulation of type VI secretion gene clusters by sigma54 and cognate enhancer binding proteins.

Authors:  Christophe S Bernard; Yannick R Brunet; Marthe Gavioli; Roland Lloubès; Eric Cascales
Journal:  J Bacteriol       Date:  2011-03-04       Impact factor: 3.490

8.  Probing the assembly of transcription initiation complexes through changes in sigmaN protease sensitivity.

Authors:  P Casaz; M Buck
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

9.  Binding affinity of Escherichia coli RNA polymerase*sigma54 holoenzyme for the glnAp2, nifH and nifL promoters.

Authors:  Sabine K Vogel; Alexandra Schulz; Karsten Rippe
Journal:  Nucleic Acids Res       Date:  2002-09-15       Impact factor: 16.971

10.  Genes that protect against the host-killing activity of the E3 protein of Bacillus subtilis bacteriophage SPO1.

Authors:  P Wei; C R Stewart
Journal:  J Bacteriol       Date:  1995-05       Impact factor: 3.490

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