tmRNA engages the bacterial ribosome in a unique process termed """"""""trans-translation"""""""" that challenges the standard model of protein translation, in that mRNA molecules are switched during the synthesis of a single polypeptide, switching from the end of a """"""""broken"""""""" mRNA (lacking a stop codon) to a reading frame within tmRNA. Physiological, genetic, biochemical, structural and phylogenetic approaches will be brought to bear on the broad, long-term objectives of this proposal: 1) to understand in mechanistic detail how trans-translation is accomplished, then test predictions made by the trans-translation mechanism concerning normal translation, so as to produce a unified picture of ribosome function, and 2) to understand the roles that tmRNA and trans-translation fill in the various physiological states and adaptive responses that cells undergo. Public health benefits from inhibiting bacterial infection, and biotechnological protein synthetic applications may ultimately accrue as new ways to control the ribosome emerge from the exploration of tmRNA function.
Specific aims are to: 1) Identify biological roles of tmRNA in a survey of various physiological settings, evaluating benefits that tmRNA provides to the cell (using a previously developed competitive growth approach), and monitoring tmRNA expression levels. 2) Reveal structure/function relationships in the tmRNA molecule, applying previously developed methods for randomization/selection and in vivo assay of variant tmRNAs. 3) Search for factors that interact with tmRNA using genetic and biochemical approaches, identifying any complexes outside of the ribosome that include tmRNA. 4) Develop a staged in vitro trans-translation system to isolate the various complexes produced as tmRNA traverses the ribosome. 5) Analyze structure of tmRNA alone and in trans-translation complexes by chemical probing, cross-linking, crystallographic, and electron micrographic (the latter two collaborative) approaches.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM059881-05
Application #
6607637
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Rhoades, Marcus M
Project Start
1999-08-01
Project End
2005-07-31
Budget Start
2003-08-01
Budget End
2005-07-31
Support Year
5
Fiscal Year
2003
Total Cost
$278,768
Indirect Cost
Name
Indiana University Bloomington
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401
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Williams, Kelly P (2003) Traffic at the tmRNA gene. J Bacteriol 185:1059-70
Williams, Kelly P (2002) The tmRNA Website: invasion by an intron. Nucleic Acids Res 30:179-82
Gaudin, Cyril; Zhou, Xiong; Williams, Kelly P et al. (2002) Two-piece tmRNA in cyanobacteria and its structural analysis. Nucleic Acids Res 30:2018-24
Williams, Kelly P (2002) Integration sites for genetic elements in prokaryotic tRNA and tmRNA genes: sublocation preference of integrase subfamilies. Nucleic Acids Res 30:866-75
Williams, Kelly P (2002) Descent of a split RNA. Nucleic Acids Res 30:2025-30
Keiler, K C; Shapiro, L; Williams, K P (2000) tmRNAs that encode proteolysis-inducing tags are found in all known bacterial genomes: A two-piece tmRNA functions in Caulobacter. Proc Natl Acad Sci U S A 97:7778-83