Evidence for a second class of S-adenosylmethionine riboswitches and other regulatory RNA motifs in alpha-proteobacteria

BackgroundRiboswitches are RNA elements in the 5' untranslated leaders of bacterial mRNAs that directly sense the levels of specific metabolites with a structurally conserved aptamer domain to regulate expression of downstream genes. Riboswitches are most common in the genomes of low GC Gram-positive bacteria (for example, Bacillus subtilis contains examples of all known riboswitches), and some riboswitch classes seem to be restricted to this group.ResultsWe used comparative sequence analysis and structural probing to identify five RNA elements (serC, speF, suhB, ybhL, and metA) that reside in the intergenic regions of Agrobacterium tumefaciens and many other α-proteobacteria. One of these, the metA motif, is found upstream of methionine biosynthesis genes and binds S-adenosylmethionine (SAM). This natural aptamer most likely functions as a SAM riboswitch (SAM-II) with a consensus sequence and structure that is distinct from the class of SAM riboswitches (SAM-I) predominantly found in Gram-positive bacteria. The minimal functional SAM-II aptamer consists of fewer than 70 nucleotides, which form a single stem and a pseudoknot. Despite its simple architecture and lower affinity for SAM, the SAM-II aptamer strongly discriminates against related compounds.ConclusionSAM-II is the only metabolite-binding riboswitch class identified so far that is not found in Gram-positive bacteria, and its existence demonstrates that biological systems can use multiple RNA structures to sense a single chemical compound. The two SAM riboswitches might be 'RNA World' relics that were selectively retained in certain bacterial lineages or new motifs that have emerged since the divergence of the major bacterial groups.

[1]  H. Schwalbe,et al.  An intermolecular base triple as the basis of ligand specificity and affinity in the guanine- and adenine-sensing riboswitch RNAs. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[2]  M. Gelfand,et al.  Comparative genomics of the methionine metabolism in Gram-positive bacteria: a variety of regulatory systems. , 2004, Nucleic acids research.

[3]  Jeffrey E. Barrick,et al.  Riboswitches Control Fundamental Biochemical Pathways in Bacillus subtilis and Other Bacteria , 2003, Cell.

[4]  B. Ganem RNA world , 1987, Nature.

[5]  Zasha Weinberg,et al.  A Glycine-Dependent Riboswitch That Uses Cooperative Binding to Control Gene Expression , 2004, Science.

[6]  Y. Lu,et al.  Function of RNA secondary structures in transcriptional attenuation of the Bacillus subtilis pyr operon. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[7]  L. Shapiro,et al.  Identification of Long Intergenic Repeat Sequences Associated with DNA Methylation Sites in Caulobacter crescentus and Other α-Proteobacteria , 2003, Journal of bacteriology.

[8]  James M. Carothers,et al.  Informational Complexity and Functional Activity of RNA Structures , 2004, Journal of the American Chemical Society.

[9]  Ali Nahvi,et al.  Genetic control by a metabolite binding mRNA. , 2002, Chemistry & biology.

[10]  D. Crothers,et al.  The speed of RNA transcription and metabolite binding kinetics operate an FMN riboswitch. , 2005, Molecular cell.

[11]  G. F. Joyce The antiquity of RNA-based evolution , 2002, Nature.

[12]  R. Breaker,et al.  Gene regulation by riboswitches , 2004, Nature Reviews Molecular Cell Biology.

[13]  Margaret S. Ebert,et al.  An mRNA structure in bacteria that controls gene expression by binding lysine. , 2003, Genes & development.

[14]  G. Haba,et al.  S-Adenosylmethionine: The Relation of Configuration at the Sulfonium Center to Enzymatic Reactivity1 , 1959 .

[15]  Sean R. Eddy,et al.  Rfam: an RNA family database , 2003, Nucleic Acids Res..

[16]  O. White,et al.  Environmental Genome Shotgun Sequencing of the Sargasso Sea , 2004, Science.

[17]  R. Breaker,et al.  An mRNA structure that controls gene expression by binding FMN , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[18]  Evgeny Nudler,et al.  Sensing Small Molecules by Nascent RNA A Mechanism to Control Transcription in Bacteria , 2002, Cell.

[19]  R. Nielsen A conserved RNA structure element involved in the regulation of bacterial riboflavin synthesis genes , 2022 .

[20]  Jeffrey E. Barrick,et al.  New RNA motifs suggest an expanded scope for riboswitches in bacterial genetic control. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[21]  A. Serganov,et al.  Structural basis for discriminative regulation of gene expression by adenine- and guanine-sensing mRNAs. , 2004, Chemistry & biology.

[22]  R. Borchardt,et al.  Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 5. Role of the asymmetric sulfonium pole in the enzymatic binding of S-adenosyl-L-methionine. , 1976, Journal of medicinal chemistry.

[23]  T. Henkin,et al.  Transcription termination control of the S box system: Direct measurement of S-adenosylmethionine by the leader RNA , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[24]  Darren A. Natale,et al.  The COG database: an updated version includes eukaryotes , 2003, BMC Bioinformatics.

[25]  R. Breaker,et al.  Control of gene expression by a natural metabolite-responsive ribozyme , 2004, Nature.

[26]  R. Borchardt,et al.  Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 2. Modification of the base portion of S-adenosylhomocysteine , 1974 .

[27]  E. Dolence,et al.  Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 8. Molecular dissections of carbocyclic 3-deazaadenosine as inhibitors of S-adenosylhomocysteine hydrolase. , 1985, Journal of medicinal chemistry.

[28]  R. Breaker,et al.  Adenine riboswitches and gene activation by disruption of a transcription terminator , 2004, Nature Structural &Molecular Biology.

[29]  J. Szostak,et al.  Evolution of aptamers with a new specificity and new secondary structures from an ATP aptamer. , 2003, RNA.

[30]  Jeffrey E. Barrick,et al.  Coenzyme B12 riboswitches are widespread genetic control elements in prokaryotes. , 2004, Nucleic acids research.

[31]  L. Samson,et al.  Influence of S-Adenosylmethionine Pool Size on Spontaneous Mutation, Dam Methylation, and Cell Growth ofEscherichia coli , 1999, Journal of bacteriology.

[32]  David Penny,et al.  Relics from the RNA World , 1998, Journal of Molecular Evolution.

[33]  Vitaly Epshtein,et al.  The riboswitch-mediated control of sulfur metabolism in bacteria , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[34]  Zasha Weinberg,et al.  Exploiting conserved structure for faster annotation of non-coding RNAs without loss of accuracy , 2004, ISMB/ECCB.

[35]  T. Henkin Transcription termination control in bacteria. , 2000, Current opinion in microbiology.

[36]  K. Wassarman Small RNAs in Bacteria Diverse Regulators of Gene Expression in Response to Environmental Changes , 2002, Cell.

[37]  R R Breaker,et al.  Relationship between internucleotide linkage geometry and the stability of RNA. , 1999, RNA.

[38]  M. Gelfand,et al.  Attenuation regulation of amino acid biosynthetic operons in proteobacteria: comparative genomics analysis. , 2004, FEMS microbiology letters.

[39]  Jack W. Szostak,et al.  A Small Aptamer with Strong and Specific Recognition of the Triphosphate of ATP , 2004, Journal of the American Chemical Society.

[40]  S A Benner,et al.  Modern metabolism as a palimpsest of the RNA world. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[41]  M. Osteras,et al.  Identification of Rhizobium-specific intergenic mosaic elements within an essential two-component regulatory system of Rhizobium species , 1995, Journal of bacteriology.

[42]  Ali Nahvi,et al.  An mRNA structure that controls gene expression by binding S-adenosylmethionine , 2003, Nature Structural Biology.

[43]  E. Nudler,et al.  The riboswitch control of bacterial metabolism. , 2004, Trends in biochemical sciences.

[44]  Larry Gold,et al.  One, two, infinity: genomes filled with aptamers. , 2002, Chemistry & biology.

[45]  R. Borchardt,et al.  Potential inhibitor of S-adenosylmethionine-dependent methyltransferases. 2. Modification of the base portion of S-adenosylhomocysteine. , 1974, Journal of medicinal chemistry.

[46]  H. White Coenzymes as fossils of an earlier metabolic state , 1976, Journal of Molecular Evolution.

[47]  R. Borchardt,et al.  Potential inhibitors of S-adenosylmethionine-dependent methyltransferases. 3. Modifications of the sugar portion of S-adenosylhomocysteine. , 1975, Journal of medicinal chemistry.

[48]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[49]  Jack W. Szostak,et al.  An RNA motif that binds ATP , 1993, Nature.