Literature DB >> 14597663

An mRNA structure in bacteria that controls gene expression by binding lysine.

Narasimhan Sudarsan1, J Kenneth Wickiser, Shingo Nakamura, Margaret S Ebert, Ronald R Breaker.   

Abstract

Riboswitches are metabolite-responsive genetic control elements that reside in the untranslated regions (UTRs) of certain messenger RNAs. Herein, we report that the 5'-UTR of the lysC gene of Bacillus subtilis carries a conserved RNA element that serves as a lysine-responsive riboswitch. The ligand-binding domain of the riboswitch binds to L-lysine with an apparent dissociation constant (KD) of approximately 1 micro M, and exhibits a high level of molecular discrimination against closely related analogs, including D-lysine and ornithine. Furthermore, we provide evidence that this widespread class of riboswitches serves as a target for the antimetabolite S-(2-aminoethyl)-L-cysteine (AEC). These findings add support to the hypotheses that direct sensing of metabolites by messenger RNAs is a fundamental form of genetic control and that riboswitches represent a new class of antimicrobial drug targets.

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Year:  2003        PMID: 14597663      PMCID: PMC280618          DOI: 10.1101/gad.1140003

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


  28 in total

1.  Aspartokinase III repression and lysine analogs utilization for protein synthesis.

Authors:  M Di Girolamo; V Busiello; R Coccia; C Foppoli
Journal:  Physiol Chem Phys Med NMR       Date:  1990

2.  Fine-structure mapping of cis-acting control sites in the lysC operon of Bacillus subtilis.

Authors:  Y Lu; T N Shevtchenko; H Paulus
Journal:  FEMS Microbiol Lett       Date:  1992-04-01       Impact factor: 2.742

3.  Regulation of dihydrodipicolinate synthase and aspartate kinase in Bacillus subtilis.

Authors:  B Vold; J Szulmajster; A Carbone
Journal:  J Bacteriol       Date:  1975-03       Impact factor: 3.490

4.  Isolation and identification of mutants constitutive for aspartokinase III synthesis in Escherichia coli K 12.

Authors:  E Boy; F Borne; J C Patte
Journal:  Biochimie       Date:  1979       Impact factor: 4.079

5.  A common motif organizes the structure of multi-helix loops in 16 S and 23 S ribosomal RNAs.

Authors:  N B Leontis; E Westhof
Journal:  J Mol Biol       Date:  1998-10-30       Impact factor: 5.469

6.  Analysis of the regulatory region of the lysC gene of Escherichia coli.

Authors:  H H Liao; T H Hseu
Journal:  FEMS Microbiol Lett       Date:  1998-11-01       Impact factor: 2.742

7.  Quantitative analysis of transcriptional pausing by Escherichia coli RNA polymerase: his leader pause site as paradigm.

Authors:  R Landick; D Wang; C L Chan
Journal:  Methods Enzymol       Date:  1996       Impact factor: 1.600

8.  Nucleotide sequence of the Escherichia coli cad operon: a system for neutralization of low extracellular pH.

Authors:  S Y Meng; G N Bennett
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

9.  Lysine-induced premature transcription termination in the lysC operon of Bacillus subtilis.

Authors:  S Kochhar; H Paulus
Journal:  Microbiology       Date:  1996-07       Impact factor: 2.777

10.  Cloning and nucleotide sequence of the gene coding for aspartokinase II from a thermophilic methylotrophic Bacillus sp.

Authors:  F J Schendel; M C Flickinger
Journal:  Appl Environ Microbiol       Date:  1992-09       Impact factor: 4.792

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  145 in total

1.  Bacterial lysine decarboxylase influences human dental biofilm lysine content, biofilm accumulation, and subclinical gingival inflammation.

Authors:  Zsolt Lohinai; Beata Keremi; Eva Szoko; Tamas Tabi; Csaba Szabo; Zsolt Tulassay; Martin Levine
Journal:  J Periodontol       Date:  2011-12-05       Impact factor: 6.993

2.  A nascent polypeptide domain that can regulate translation elongation.

Authors:  Peng Fang; Christina C Spevak; Cheng Wu; Matthew S Sachs
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-12       Impact factor: 11.205

3.  New RNA motifs suggest an expanded scope for riboswitches in bacterial genetic control.

Authors:  Jeffrey E Barrick; Keith A Corbino; Wade C Winkler; Ali Nahvi; Maumita Mandal; Jennifer Collins; Mark Lee; Adam Roth; Narasimhan Sudarsan; Inbal Jona; J Kenneth Wickiser; Ronald R Breaker
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-19       Impact factor: 11.205

4.  A theophylline responsive riboswitch based on helix slipping controls gene expression in vivo.

Authors:  Beatrix Suess; Barbara Fink; Christian Berens; Régis Stentz; Wolfgang Hillen
Journal:  Nucleic Acids Res       Date:  2004-03-05       Impact factor: 16.971

5.  Evidence for widespread gene control function by the ydaO riboswitch candidate.

Authors:  Kirsten F Block; Ming C Hammond; Ronald R Breaker
Journal:  J Bacteriol       Date:  2010-05-28       Impact factor: 3.490

6.  Identification of a tertiary interaction important for cooperative ligand binding by the glycine riboswitch.

Authors:  Thanh V Erion; Scott A Strobel
Journal:  RNA       Date:  2010-11-23       Impact factor: 4.942

Review 7.  Riboswitch structure in the ligand-free state.

Authors:  Joseph A Liberman; Joseph E Wedekind
Journal:  Wiley Interdiscip Rev RNA       Date:  2011-09-28       Impact factor: 9.957

8.  Role of lysine binding residues in the global folding of the lysC riboswitch.

Authors:  Erich Smith-Peter; Anne-Marie Lamontagne; Daniel A Lafontaine
Journal:  RNA Biol       Date:  2015       Impact factor: 4.652

Review 9.  Themes and variations in riboswitch structure and function.

Authors:  Alla Peselis; Alexander Serganov
Journal:  Biochim Biophys Acta       Date:  2014-02-28

Review 10.  Computational analysis of riboswitch-based regulation.

Authors:  Eric I Sun; Dmitry A Rodionov
Journal:  Biochim Biophys Acta       Date:  2014-02-28
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