Approximately 40 percent of the total energy production of E. coli is consumed to synthesize the large number of ribosomal components, 3 RNAs totaling over 4000 nucleotides and greater than 50 proteins. In bacteria, the rates of cell growth and ribosome biosynthesis are intimately related and directly correlated. Thus, for cell viability, the synthesis of ribosomal components and their subsequent assembly must be coordinated. These observations suggest that an accurately assembled and functional ribosome is one of the most important cellular organelles and that defects in ribosome assembly would be fatal. Although, years of research have been dedicated to studying ribosomal components and ribosome function, the pathway(s) and dynamics of ribosome assembly remain largely uncharacterized despite general importance to cell physiology. This proposal describes three approaches to study the mechanism, pathway and dynamics of ribosome assembly. The goal of this proposal is to understand what factors are involved in and critical for E. coli 30S ribosomal subunit assembly. First, in vitro reconstitution of 30S subunits using a complete set of recombinant small subunit ribosomal proteins will be used to identify l6S rRNA nucleotides and small subunit ribosomal proteins involved in 30S subunit assembly. Second, a combination of solution chemical probing and small subunit ribosomal protein-directed hydroxyl radical probing will be used to map 16S rRNA folding during different stages of 30S subunit formation. Lastly, in vitro reconstitution and standard biochemical approaches will be used to purify and characterize cellular (extra-ribosomal) factors involved in ribosome assembly. Preliminary results suggest that all three specific aims will add to our understanding of ribosome assembly. Insights gained in these studies will allow us to pursue future experiments studying ribosome biogenesis in vivo. In addition, these studies may identify targets for regulation of bacterial cell growth and perhaps lead to the production of novel antimicrobials.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM062432-04
Application #
6704175
Study Section
Biochemistry Study Section (BIO)
Program Officer
Rhoades, Marcus M
Project Start
2001-03-01
Project End
2006-02-28
Budget Start
2004-03-01
Budget End
2005-02-28
Support Year
4
Fiscal Year
2004
Total Cost
$206,906
Indirect Cost
Name
Iowa State University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
005309844
City
Ames
State
IA
Country
United States
Zip Code
50011
Napper, Nathan; Culver, Gloria M (2015) Analysis of r-protein and RNA conformation of 30S subunit intermediates in bacteria. RNA 21:1323-34
Gupta, Neha; Culver, Gloria M (2014) Multiple in vivo pathways for Escherichia coli small ribosomal subunit assembly occur on one pre-rRNA. Nat Struct Mol Biol 21:937-43
Connolly, Keith; Culver, Gloria (2013) Overexpression of RbfA in the absence of the KsgA checkpoint results in impaired translation initiation. Mol Microbiol 87:968-81
Desai, Pooja M; Culver, Gloria M; Rife, Jason P (2011) Site-directed mutants of 16S rRNA reveal important RNA domains for KsgA function and 30S subunit assembly. Biochemistry 50:854-63
Calidas, Deepika; Culver, Gloria M (2011) Interdependencies govern multidomain architecture in ribosomal small subunit assembly. RNA 17:263-77
Xu, Zhili; Culver, Gloria M (2010) Differential assembly of 16S rRNA domains during 30S subunit formation. RNA 16:1990-2001
Roy-Chaudhuri, Biswajoy; Kirthi, Narayanaswamy; Culver, Gloria M (2010) Appropriate maturation and folding of 16S rRNA during 30S subunit biogenesis are critical for translational fidelity. Proc Natl Acad Sci U S A 107:4567-72
Connolly, Keith; Culver, Gloria (2009) Deconstructing ribosome construction. Trends Biochem Sci 34:256-63
Xu, Zhili; Culver, Gloria M (2009) Chemical probing of RNA and RNA/protein complexes. Methods Enzymol 468:147-65
Connolly, Keith; Rife, Jason P; Culver, Gloria (2008) Mechanistic insight into the ribosome biogenesis functions of the ancient protein KsgA. Mol Microbiol 70:1062-75

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