Literature DB >> 11443133

Different roles for basic and aromatic amino acids in conserved region 2 of Escherichia coli sigma(70) in the nucleation and maintenance of the single-stranded DNA bubble in open RNA polymerase-promoter complexes.

M Tomsic1, L Tsujikawa, G Panaghie, Y Wang, J Azok, P L deHaseth.   

Abstract

Amino acid residues in region 2 of final sigma(70) have been shown to play an important role in the strand separation step that is necessary for formation of the functional or open RNA polymerase-promoter complex. Here we present a comparison of the roles of basic and aromatic amino acids in the accomplishment of this process, using RNA polymerase bearing alanine substitutions for both types of amino acids in region 2. We determined the effects of the substitutions on the kinetics of open complex formation, as well as on the ability of the RNA polymerase to form complexes with single-stranded DNA, and with forked DNA duplexes carrying a single-stranded overhang consisting of bases in the -10 region. We concluded that two basic amino acids (Lys(414) and Lys(418)) are important for promoter binding and demonstrated distinct roles, at a subsequent step, for two aromatic amino acids (Tyr(430) and Trp(433)). It is likely that these four amino acids, which are close to each other in the structure of final sigma(70), together are involved in the nucleation of the strand separation process.

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Year:  2001        PMID: 11443133     DOI: 10.1074/jbc.M105027200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  34 in total

1.  Interaction of RNA polymerase with forked DNA: evidence for two kinetically significant intermediates on the pathway to the final complex.

Authors:  Laura Tsujikawa; Oleg V Tsodikov; Pieter L deHaseth
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-12       Impact factor: 11.205

2.  Structure-function studies of Escherichia coli RpoH (sigma32) by in vitro linker insertion mutagenesis.

Authors:  Franz Narberhaus; Sylvia Balsiger
Journal:  J Bacteriol       Date:  2003-05       Impact factor: 3.490

3.  Effect of DNA bases and backbone on sigma70 holoenzyme binding and isomerization using fork junction probes.

Authors:  Mike S Fenton; Jay D Gralla
Journal:  Nucleic Acids Res       Date:  2003-06-01       Impact factor: 16.971

4.  Structural basis for promoter-10 element recognition by the bacterial RNA polymerase σ subunit.

Authors:  Andrey Feklistov; Seth A Darst
Journal:  Cell       Date:  2011-12-01       Impact factor: 41.582

5.  Interaction of Escherichia coli RNA polymerase σ70 subunit with promoter elements in the context of free σ70, RNA polymerase holoenzyme, and the β'-σ70 complex.

Authors:  Vladimir Mekler; Olga Pavlova; Konstantin Severinov
Journal:  J Biol Chem       Date:  2010-10-15       Impact factor: 5.157

6.  Lineage-specific amino acid substitutions in region 2 of the RNA polymerase sigma subunit affect the temperature of promoter opening.

Authors:  N Barinova; E Zhilina; I Bass; V Nikiforov; A Kulbachinskiy
Journal:  J Bacteriol       Date:  2008-02-15       Impact factor: 3.490

Review 7.  Advances in bacterial promoter recognition and its control by factors that do not bind DNA.

Authors:  Shanil P Haugen; Wilma Ross; Richard L Gourse
Journal:  Nat Rev Microbiol       Date:  2008-06-03       Impact factor: 60.633

8.  Reduced capacity of alternative sigmas to melt promoters ensures stringent promoter recognition.

Authors:  Byoung-Mo Koo; Virgil A Rhodius; Gen Nonaka; Pieter L deHaseth; Carol A Gross
Journal:  Genes Dev       Date:  2009-10-15       Impact factor: 11.361

9.  Promoter recognition by bacterial alternative sigma factors: the price of high selectivity?

Authors:  Andrey Feklistov; Seth A Darst
Journal:  Genes Dev       Date:  2009-10-15       Impact factor: 11.361

10.  Threonine 429 of Escherichia coli sigma 70 is a key participant in promoter DNA melting by RNA polymerase.

Authors:  Lisa A Schroeder; Mary E Karpen; Pieter L deHaseth
Journal:  J Mol Biol       Date:  2007-11-28       Impact factor: 5.469

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