Related Content
Search Google Scholar for:
|
Genes & Dev. 16 (13): 1696-1706
Copyright © 2002 by Cold Spring Harbor Laboratory Press.
Vol. 16, No. 13, pp. 1696-1706, July 1, 2002
RESEARCH PAPER
Spot 42 RNA mediates discoordinate expression of the E. coli galactose operon
Thorleif
Møller,
Thomas
Franch,
Christina
Udesen,
Kenn
Gerdes, and
Poul
Valentin-Hansen1
Department of Biochemistry and Molecular Biology, University of
Southern Denmark, Campusvej 55, DK-5230 Odense M, Denmark
The physiological role of Escherichia coli Spot 42 RNA has
remained obscure, even though the 109-nucleotide RNA was discovered almost three decades ago. Structural features of Spot 42 RNA and previous work suggested to us that the RNA might be a regulator of
discoordinate gene expression of the galactose operon, a control that
is only understood at the phenomenological level. The effects of
controlled expression of Spot 42 RNA or deleting the gene (spf) encoding the RNA supported this hypothesis. Down-regulation of galK expression, the third gene in the gal operon, was
only observed in the presence of Spot 42 RNA and required growth
conditions that caused derepression of the spf gene. Subsequent
biochemical studies showed that Spot 42 RNA specifically bound at the
galK Shine-Dalgarno region of the galETKM mRNA, thereby
blocking ribosome binding. We conclude that Spot 42 RNA is an antisense
RNA that acts to differentially regulate genes that are expressed from the same transcription unit. Our results reveal an interesting mechanism by which the expression of a promoter distal gene in an
operon can be modulated and underline the importance of antisense control in bacterial gene regulation.
[Key Words:
Antisense RNA; galactose operon; riboregulation; small RNAs; Spot 42 RNA; translational regulation]
1
Corresponding author.
GENES & DEVELOPMENT 16:1696-1706 © 2002 by Cold Spring Harbor Laboratory Press ISSN 0890-9369/02 $5.00
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
- Small RNA binding-site multiplicity involved in translational regulation of a polycistronic mRNA.
- J. B. Rice, D. Balasubramanian, and C. K. Vanderpool (2012)
PNAS
109, E2691-E2698
| Abstract »
| Full Text »
| PDF »
- Noncanonical repression of translation initiation through small RNA recruitment of the RNA chaperone Hfq.
- G. Desnoyers and E. Masse (2012)
Genes & Dev.
26, 726-739
| Abstract »
| Full Text »
| PDF »
- The Vibrio cholerae Mannitol Transporter Is Regulated Posttranscriptionally by the MtlS Small Regulatory RNA.
- L. M. Mustachio, S. Aksit, R. H. Mistry, R. Scheffler, A. Yamada, and J. M. Liu (2012)
J. Bacteriol.
194, 598-606
| Abstract »
| Full Text »
| PDF »
- Streptomyces coelicolor sRNA scr5239 inhibits agarase expression by direct base pairing to the dagA coding region.
- M.-P. Vockenhuber and B. Suess (2012)
Microbiology
158, 424-435
| Abstract »
| Full Text »
| PDF »
- Translational Repression of NhaR, a Novel Pathway for Multi-Tier Regulation of Biofilm Circuitry by CsrA.
- A. Pannuri, H. Yakhnin, C. A. Vakulskas, A. N. Edwards, P. Babitzke, and T. Romeo (2012)
J. Bacteriol.
194, 79-89
| Abstract »
| Full Text »
| PDF »
- Locked Nucleic Acid and Flow Cytometry-Fluorescence In Situ Hybridization for the Detection of Bacterial Small Noncoding RNAs.
- K. L. Robertson and G. J. Vora (2012)
Appl. Envir. Microbiol.
78, 14-20
| Abstract »
| Full Text »
| PDF »
- Bacterial Small RNA Regulators: Versatile Roles and Rapidly Evolving Variations.
- S. Gottesman and G. Storz (2011)
Cold Spring Harb Perspect Biol
3, a003798
| Abstract »
| Full Text »
| PDF »
- Functional characterization of bacterial sRNAs using a network biology approach.
- S. R. Modi, D. M. Camacho, M. A. Kohanski, G. C. Walker, and J. J. Collins (2011)
PNAS
108, 15522-15527
| Abstract »
| Full Text »
| PDF »
- Structure and Function of the D-Galactose Network in Enterobacteria.
- Z. Csiszovszki, S. Krishna, L. Orosz, S. Adhya, and S. Semsey (2011)
mBio
2, e00053-11
| Abstract »
| Full Text »
| PDF »
- Quantifying the sequence-function relation in gene silencing by bacterial small RNAs.
- Y. Hao, Z. J. Zhang, D. W. Erickson, M. Huang, Y. Huang, J. Li, T. Hwa, and H. Shi (2011)
PNAS
108, 12473-12478
| Abstract »
| Full Text »
| PDF »
- The small RNA SgrS controls sugar-phosphate accumulation by regulating multiple PTS genes.
- J. B. Rice and C. K. Vanderpool (2011)
Nucleic Acids Res.
39, 3806-3819
| Abstract »
| Full Text »
| PDF »
- Artificial trans-encoded small non-coding RNAs specifically silence the selected gene expression in bacteria.
- S. Man, R. Cheng, C. Miao, Q. Gong, Y. Gu, X. Lu, F. Han, and W. Yu (2011)
Nucleic Acids Res.
39, e50
| Abstract »
| Full Text »
| PDF »
- Accessibility and Evolutionary Conservation Mark Bacterial Small-RNA Target-Binding Regions.
- A. Peer and H. Margalit (2011)
J. Bacteriol.
193, 1690-1701
| Abstract »
| Full Text »
| PDF »
- The stoichiometry of the Escherichia coli Hfq protein bound to RNA.
- T. B. Updegrove, J. J. Correia, Y. Chen, C. Terry, and R. M. Wartell (2011)
RNA
17, 489-500
| Abstract »
| Full Text »
| PDF »
- Timing of Gene Transcription in the Galactose Utilization System of Escherichia coli.
- P. Horvath, A. Hunziker, J. Erdossy, S. Krishna, and S. Semsey (2010)
J. Biol. Chem.
285, 38062-38068
| Abstract »
| Full Text »
| PDF »
- Evidence for an autonomous 5' target recognition domain in an Hfq-associated small RNA.
- K. Papenfort, M. Bouvier, F. Mika, C. M. Sharma, and J. Vogel (2010)
PNAS
107, 20435-20440
| Abstract »
| Full Text »
| PDF »
- The Archaeal Lsm Protein Binds to Small RNAs.
- S. Fischer, J. Benz, B. Spath, L.-K. Maier, J. Straub, M. Granzow, M. Raabe, H. Urlaub, J. Hoffmann, B. Brutschy, et al. (2010)
J. Biol. Chem.
285, 34429-34438
| Abstract »
| Full Text »
| PDF »
- The Crc Global Regulator Inhibits the Pseudomonas putida pWW0 Toluene/Xylene Assimilation Pathway by Repressing the Translation of Regulatory and Structural Genes.
- R. Moreno, P. Fonseca, and F. Rojo (2010)
J. Biol. Chem.
285, 24412-24419
| Abstract »
| Full Text »
| PDF »
- Identification of non-coding RNAs in environmental vibrios.
- A. C. G. Silveira, K. L. Robertson, B. Lin, Z. Wang, G. J. Vora, A. T. R. Vasconcelos, and F. L. Thompson (2010)
Microbiology
156, 2452-2458
| Abstract »
| Full Text »
| PDF »
- Impact of the RNA chaperone Hfq on multidrug resistance in Escherichia coli.
- J. Yamada, S. Yamasaki, H. Hirakawa, M. Hayashi-Nishino, A. Yamaguchi, and K. Nishino (2010)
J. Antimicrob. Chemother.
65, 853-858
| Abstract »
| Full Text »
| PDF »
- Dynamic features of gene expression control by small regulatory RNAs.
- N. Mitarai, J.-A. M. Benjamin, S. Krishna, S. Semsey, Z. Csiszovszki, E. Masse, and K. Sneppen (2009)
PNAS
106, 10655-10659
| Abstract »
| Full Text »
| PDF »
- Specific gene silencing by artificial trans-encoded small noncoding RNAs in bacteria.
- R. Cheng, C. Miao, Q. Gong, Y. Gu, X. Lu, F. Han, and W. Yu (2009)
Nucleic Acids Res.
| Abstract »
| Full Text »
| PDF »
- Identification of RNA molecules by specific enzyme digestion and mass spectrometry: software for and implementation of RNA mass mapping.
- R. Matthiesen and F. Kirpekar (2009)
Nucleic Acids Res.
37, e48
| Abstract »
| Full Text »
| PDF »
- The Crp-Activated Small Noncoding Regulatory RNA CyaR (RyeE) Links Nutritional Status to Group Behavior.
- N. De Lay and S. Gottesman (2009)
J. Bacteriol.
191, 461-476
| Abstract »
| Full Text »
| PDF »
- Role of the sRNA GcvB in regulation of cycA in Escherichia coli.
- S. C. Pulvermacher, L. T. Stauffer, and G. V. Stauffer (2009)
Microbiology
155, 106-114
| Abstract »
| Full Text »
| PDF »
- IntaRNA: efficient prediction of bacterial sRNA targets incorporating target site accessibility and seed regions.
- A. Busch, A. S. Richter, and R. Backofen (2008)
Bioinformatics
24, 2849-2856
| Abstract »
| Full Text »
| PDF »
- RNAplex: a fast tool for RNA-RNA interaction search.
- H. Tafer and I. L. Hofacker (2008)
Bioinformatics
24, 2657-2663
| Abstract »
| Full Text »
| PDF »
- Noncoding RNA control of the making and breaking of sugars.
- B. Gorke and J. Vogel (2008)
Genes & Dev.
22, 2914-2925
| Abstract »
| Full Text »
| PDF »
- Detection of small RNAs in Pseudomonas aeruginosa by RNomics and structure-based bioinformatic tools.
- E. Sonnleitner, T. Sorger-Domenigg, M. J. Madej, S. Findeiss, J. Hackermuller, A. Huttenhofer, P. F. Stadler, U. Blasi, and I. Moll (2008)
Microbiology
154, 3175-3187
| Abstract »
| Full Text »
| PDF »
- Trans-natural antisense transcripts including noncoding RNAs in 10 species: implications for expression regulation.
- J.-T. Li, Y. Zhang, L. Kong, Q.-R. Liu, and L. Wei (2008)
Nucleic Acids Res.
36, 4833-4844
| Abstract »
| Full Text »
| PDF »
- TargetRNA: a tool for predicting targets of small RNA action in bacteria.
- B. Tjaden (2008)
Nucleic Acids Res.
36, W109-W113
| Abstract »
| Full Text »
| PDF »
- An Hfq-like protein in archaea: Crystal structure and functional characterization of the Sm protein from Methanococcus jannaschii.
- J. S. Nielsen, A. Boggild, C. B.F. Andersen, G. Nielsen, A. Boysen, D. E. Brodersen, and P. Valentin-Hansen (2007)
RNA
13, 2213-2223
| Abstract »
| Full Text »
| PDF »
- In vitro analysis of the interaction between the small RNA SR1 and its primary target ahrC mRNA.
- N. Heidrich, I. Moll, and S. Brantl (2007)
Nucleic Acids Res.
35, 4331-4346
| Abstract »
| Full Text »
| PDF »
- The Novel Transcription Factor SgrR Coordinates the Response to Glucose-Phosphate Stress.
- C. K. Vanderpool and S. Gottesman (2007)
J. Bacteriol.
189, 2238-2248
| Abstract »
| Full Text »
| PDF »
- Identification of new noncoding RNAs in Listeria monocytogenes and prediction of mRNA targets.
- P. Mandin, F. Repoila, M. Vergassola, T. Geissmann, and P. Cossart (2007)
Nucleic Acids Res.
35, 962-974
| Abstract »
| Full Text »
| PDF »
- Translational control and target recognition by Escherichia coli small RNAs in vivo.
- J. H. Urban and J. Vogel (2007)
Nucleic Acids Res.
35, 1018-1037
| Abstract »
| Full Text »
| PDF »
- Small RNA Regulators and the Bacterial Response to Stress.
- S. GOTTESMAN, C.A. McCULLEN, M. GUILLIER, C.K. VANDERPOOL, N. MAJDALANI, J. BENHAMMOU, K.M. THOMPSON, P.C. FitzGERALD, N.A. SOWA, and D.J. FitzGERALD (2006)
Cold Spring Harb Symp Quant Biol
71, 1-11
| Abstract »
| PDF »
- Target prediction for small, noncoding RNAs in bacteria..
- B. Tjaden, S. S. Goodwin, J. A. Opdyke, M. Guillier, D. X. Fu, S. Gottesman, and G. Storz (2006)
Nucleic Acids Res.
34, 2791-2802
| Abstract »
| Full Text »
| PDF »
- Identification of a Gene Cluster for the Formation of Extracellular Polysaccharide Precursors in the Chemolithoautotroph Acidithiobacillus ferrooxidans.
- M. Barreto, E. Jedlicki, and D. S. Holmes (2005)
Appl. Envir. Microbiol.
71, 2902-2909
| Abstract »
| Full Text »
| PDF »
- The Etiological Agent of Lyme Disease, Borrelia burgdorferi, Appears To Contain Only a Few Small RNA Molecules.
- Y. Ostberg, I. Bunikis, S. Bergstrom, and J. Johansson (2004)
J. Bacteriol.
186, 8472-8477
| Abstract »
| Full Text »
| PDF »
- GadY, a Small-RNA Regulator of Acid Response Genes in Escherichia coli.
- J. A. Opdyke, J.-G. Kang, and G. Storz (2004)
J. Bacteriol.
186, 6698-6705
| Abstract »
| Full Text »
| PDF »
- 6S RNA Function Enhances Long-Term Cell Survival.
- A. E. Trotochaud and K. M. Wassarman (2004)
J. Bacteriol.
186, 4978-4985
| Abstract »
| Full Text »
| PDF »
- A Repeated GGA Motif Is Critical for the Activity and Stability of the Riboregulator RsmY of Pseudomonas fluorescens.
- C. Valverde, M. Lindell, E. G. H. Wagner, and D. Haas (2004)
J. Biol. Chem.
279, 25066-25074
| Abstract »
| Full Text »
| PDF »
- Coupled degradation of a small regulatory RNA and its mRNA targets in Escherichia coli.
- E. Masse, F. E. Escorcia, and S. Gottesman (2003)
Genes & Dev.
17, 2374-2383
| Abstract »
| Full Text »
| PDF »
- Suboperonic Regulatory Signals.
- S. Adhya (2003)
Sci. STKE
2003, pe22
| Abstract »
| Full Text »
| PDF »
- Expression of the glycolytic gapA operon in Bacillus subtilis: differential syntheses of proteins encoded by the operon.
- C. Meinken, H.-M. Blencke, H. Ludwig, and J. Stulke (2003)
Microbiology
149, 751-761
| Abstract »
| Full Text »
| PDF »
- Stealth regulation: biological circuits with small RNA switches.
- S. Gottesman (2002)
Genes & Dev.
16, 2829-2842
| Full Text »
| PDF »
|
|