Literature DB >> 12963366

Hyperthermophilic Thermotoga arginine repressor binding to full-length cognate and heterologous arginine operators and to half-site targets.

Amélie Morin1, Nadine Huysveld, Frédérique Braun, Diliana Dimova, Vehary Sakanyan, Daniel Charlier.   

Abstract

The degree of sequence conservation of arginine repressor proteins (ArgR) and of the cognate operators (tandem pairs of 18 bp imperfect palindromes, ARG boxes) in evolutionarily distant bacteria is unusually high, and the global mechanism of ArgR-mediated regulation appears to be similar. However, here we demonstrate that the arginine repressor from the hyperthermophilic bacterium Thermotoga neapolitana (ArgR(Tn)) exhibits characteristics that clearly distinguish this regulator from the well-studied homologues from Escherichia coli, Bacillus subtilis and B.stearothermophilus. A high-resolution contact map of ArgR(Tn) binding to the operator of the biosynthetic argGHCJBD operon of Thermotoga maritima indicates that ArgR(Tn) establishes all of its strong contacts with a single ARG box-like sequence of the operator only. Protein array and electrophoretic mobility-shift data demonstrate that ArgR(Tn) has a remarkable capacity to bind to arginine operators from Gram-negative and Gram-positive bacteria, and to single ARG box-bearing targets. Moreover, the overall effect of L-arginine on the apparent K(d) of ArgR(Tn) binding to various cognate and heterologous operator fragments was minor with respect to that observed with diverse bacterial arginine repressors. We demonstrate that this unusual behaviour for an ArgR protein can, to a large extent, be ascribed to the presence of a serine residue at position 107 of ArgR(Tn), instead of the highly conserved glutamine that is involved in arginine binding in the E.coli repressor. Consistent with these results, ArR(Tn) was found to behave as a superrepressor in E.coli, inhibiting growth in minimal medium, even supplemented with arginine, whereas similar constructs bearing the S107Q mutant allele did not inhibit growth. We assume that ArgR(Tn), owing to its broad target specificity and its ability to bind single ARG box sequences, might play a more general regulatory role in Thermotoga

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12963366     DOI: 10.1016/s0022-2836(03)00951-3

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


  7 in total

1.  Crystallization and preliminary X-ray diffraction analysis of the arginine repressor of the hyperthermophile Thermotoga neapolitana.

Authors:  Jan Massant; Eveline Peeters; Daniel Charlier; Dominique Maes
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-12-16

2.  Binding-competent states for L-arginine in E. coli arginine repressor apoprotein.

Authors:  Saurabh Kumar Pandey; David Řeha; Vasilina Zayats; Milan Melichercik; Jannette Carey; Rüdiger Ettrich
Journal:  J Mol Model       Date:  2014-06-21       Impact factor: 1.810

3.  Genome-wide comprehensive analysis of transcriptional regulation by ArgR in Thermus thermophilus.

Authors:  Naoki Iwanaga; Kaori Ide; Takeshi Nagashima; Takeo Tomita; Yoshihiro Agari; Akeo Shinkai; Seiki Kuramitsu; Mariko Okada-Hatakeyema; Tomohisa Kuzuyama; Makoto Nishiyama
Journal:  Extremophiles       Date:  2014-07-29       Impact factor: 2.395

4.  Symmetric allosteric mechanism of hexameric Escherichia coli arginine repressor exploits competition between L-arginine ligands and resident arginine residues.

Authors:  Rebecca Strawn; Milan Melichercik; Michael Green; Thomas Stockner; Jannette Carey; Rüdiger Ettrich
Journal:  PLoS Comput Biol       Date:  2010-06-03       Impact factor: 4.475

5.  Two arginine repressors regulate arginine biosynthesis in Lactobacillus plantarum.

Authors:  Hervé Nicoloff; Florence Arsène-Ploetze; Cédric Malandain; Michiel Kleerebezem; Françoise Bringel
Journal:  J Bacteriol       Date:  2004-09       Impact factor: 3.490

6.  Structural Analysis and Insights into the Oligomeric State of an Arginine-Dependent Transcriptional Regulator from Bacillus halodurans.

Authors:  Young Woo Park; Jina Kang; Hyun Ku Yeo; Jae Young Lee
Journal:  PLoS One       Date:  2016-05-12       Impact factor: 3.240

7.  Large-scale computational and statistical analyses of high transcription potentialities in 32 prokaryotic genomes.

Authors:  Christine Sinoquet; Sylvain Demey; Frédérique Braun
Journal:  Nucleic Acids Res       Date:  2008-04-25       Impact factor: 16.971

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.