Magnesium ions perform many essential roles in all living organisms, including enzymatic catalysis, structural integrity, and microbial pathogenesis; however, the mechanisms that regulate homeostasis are incompletely understood. Proteins are generally assumed to be the sentinels for metal ions; however, our central hypothesis is that a highly conserved metal-sensing RNA is broadly used among bacteria for posttranscriptional control of magnesium homeostasis. Given the biological distribution of this RNA element it is likely to constitute a common mode of metal ion regulation and its discovery suggests the presence of other RNA-based metal ion sensors. We have demonstrated that this RNA functions as a genetic sensor for magnesium in Bacillus subtilis, the model system for Gram-positive bacteria, and controls expression of one of the three magnesium transporter classes. Together, these data suggest that association of magnesium provokes a conformational switch within the RNA that in turn stabilizes a transcription termination signal for reduction of downstream gene expression. Based on these observations we will elucidate the mechanism of magnesium recognition by the RNA-based sensor and investigate the individual contribution of the regulatory RNA to overall magnesium homeostasis control.
The Specific Aims are to: 1). Elucidate the structural basis for metal ion detection. We will complete the three-dimensional resolution of the metal-bound RNA complex. Using additional biophysical and biochemical methods we will explore the specificity and stoichiometry of RNA-magnesium interactions, which we will also functionally test through specific substitution of RNA groups that directly coordinate to magnesium. 2). We will study the dynamical nature of metal-induced RNA folding by gel- and fluorescence-based techniques in relation to terminator formation. We will also investigate whether discontinuous transcriptional elongation is specifically coupled with these other processes as a final requirement for regulation. 3). We expect that this RNA-mediated mechanism, although vitally important, may only be one of multiple genetic mechanisms required for magnesium homeostasis. We will test this hypothesis by investigating posttranscriptional regulation of the candidate transport genes within the context of additional magnesium- regulated genes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
7R01GM081882-06
Application #
8413242
Study Section
Molecular Genetics A Study Section (MGA)
Program Officer
Reddy, Michael K
Project Start
2007-08-27
Project End
2014-07-31
Budget Start
2011-09-01
Budget End
2014-07-31
Support Year
6
Fiscal Year
2011
Total Cost
$226,442
Indirect Cost
Name
University of Maryland College Park
Department
Anatomy/Cell Biology
Type
Schools of Earth Sciences/Natur
DUNS #
790934285
City
College Park
State
MD
Country
United States
Zip Code
20742
Furukawa, Kazuhiro; Ramesh, Arati; Zhou, Zhiyuan et al. (2015) Bacterial riboswitches cooperatively bind Ni(2+) or Co(2+) ions and control expression of heavy metal transporters. Mol Cell 57:1088-1098
Shin, Jung-Ho; Wakeman, Catherine A; Goodson, Jonathan R et al. (2014) Transport of magnesium by a bacterial Nramp-related gene. PLoS Genet 10:e1004429
Wakeman, Catherine A; Goodson, Jonathan R; Zacharia, Vineetha M et al. (2014) Assessment of the requirements for magnesium transporters in Bacillus subtilis. J Bacteriol 196:1206-14
Dambach, Michael; Irnov, Irnov; Winkler, Wade C (2013) Association of RNAs with Bacillus subtilis Hfq. PLoS One 8:e55156
Ferré-D'Amaré, Adrian R; Winkler, Wade C (2011) The roles of metal ions in regulation by riboswitches. Met Ions Life Sci 9:141-73
Ramesh, Arati; Wakeman, Catherine A; Winkler, Wade C (2011) Insights into metalloregulation by M-box riboswitch RNAs via structural analysis of manganese-bound complexes. J Mol Biol 407:556-70
Irnov, Irnov; Sharma, Cynthia M; Vogel, Jorg et al. (2010) Identification of regulatory RNAs in Bacillus subtilis. Nucleic Acids Res 38:6637-51
Wakeman, Catherine A; Ramesh, Arati; Winkler, Wade C (2009) Multiple metal-binding cores are required for metalloregulation by M-box riboswitch RNAs. J Mol Biol 392:723-35
Fox, Kristina A; Ramesh, Arati; Stearns, Jennifer E et al. (2009) Multiple posttranscriptional regulatory mechanisms partner to control ethanolamine utilization in Enterococcus faecalis. Proc Natl Acad Sci U S A 106:4435-40
Dambach, Michael D; Winkler, Wade C (2009) Expanding roles for metabolite-sensing regulatory RNAs. Curr Opin Microbiol 12:161-9

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