The objective is the characterization of accessory factors that influence transcription One major goal is to extend the characterization of the functions and interactions influencing regulation of gene expression b the N protein of coliphage lambda. This interaction, which results in the generation of a transcription complex that overrides transcription termination signals (transcription antitermination), requires in addition to the lambda-encoded N protein, host Nus proteins, and an RNA site, NUT. Genetic, physiological, and biochemical studies are directed toward understanding how the participants interact to form a termination- resistant transcription complex. In addition to continuing studies on the roles of functions previously identified with N-mediated antitermination, we propose to study the roles of other factors directly implicated in modulating N action. These include a putative inhibitor of N action and the alpha subunit of RNA polymerase. A newly developed technology based on surface plasmon resonance that allows measurements of molecular interactions in real time will be employed to study interactions between participants in N-mediated antitermination. A second major goal is to extend studies on the E. coli 10Sa RNA. Our work suggests a previously unknown role for this RNA, binding of DNA- binding proteins. We propose to determine its structure of 10Sa RNA and characterize the nature of its interactions with various DNA-binding proteins, characterize the regulation its synthesis. This combination of genetic, biochemical and physiological approaches should continue to provide new information about transcription antitermination. The lambda N system will undoubtedly remain a useful model for studies on eucaryotic gene expression systems thought to be regulated by antitermination, such as the TAT regulation of HIV expression and c-myc transcription. 10Sa RNA is highly conserved and thus may play an important physiological role in nearly all, if not all, bacteria. It could play an important role in maximizing bacterial growth and thus could be a important auxiliary factor fostering pathogenesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI011459-28
Application #
6169354
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1976-09-01
Project End
2002-07-31
Budget Start
2000-08-01
Budget End
2002-07-31
Support Year
28
Fiscal Year
2000
Total Cost
$369,164
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Tyler, Jessica S; Beeri, Karen; Reynolds, Jared L et al. (2013) Prophage induction is enhanced and required for renal disease and lethality in an EHEC mouse model. PLoS Pathog 9:e1003236
Bubunenko, Mikhail; Court, Donald L; Al Refaii, Abdalla et al. (2013) Nus transcription elongation factors and RNase III modulate small ribosome subunit biogenesis in Escherichia coli. Mol Microbiol 87:382-93
Friedman, David I; Mozola, Cara C; Beeri, Karen et al. (2011) Activation of a prophage-encoded tyrosine kinase by a heterologous infecting phage results in a self-inflicted abortive infection. Mol Microbiol 82:567-77
Eaton, Kathryn A; Friedman, David I; Francis, Gayle J et al. (2008) Pathogenesis of renal disease due to enterohemorrhagic Escherichia coli in germ-free mice. Infect Immun 76:3054-63
Tyler, Jessica S; Mills, Melissa J; Friedman, David I (2004) The operator and early promoter region of the Shiga toxin type 2-encoding bacteriophage 933W and control of toxin expression. J Bacteriol 186:7670-9
Livny, Jonathan; Friedman, David I (2004) Characterizing spontaneous induction of Stx encoding phages using a selectable reporter system. Mol Microbiol 51:1691-704
Tyler, Jessica S; Friedman, David I (2004) Characterization of a eukaryotic-like tyrosine protein kinase expressed by the Shiga toxin-encoding bacteriophage 933W. J Bacteriol 186:3472-9
Zhou, Y; Mah, T F; Yu, Y T et al. (2001) Interactions of an Arg-rich region of transcription elongation protein NusA with NUT RNA: implications for the order of assembly of the lambda N antitermination complex in vivo. J Mol Biol 310:33-49
Neely, M N; Friedman, D I (2000) N-mediated transcription antitermination in lambdoid phage H-19B is characterized by alternative NUT RNA structures and a reduced requirement for host factors. Mol Microbiol 38:1074-85
Huang, C; Wolfgang, M C; Withey, J et al. (2000) Charged tmRNA but not tmRNA-mediated proteolysis is essential for Neisseria gonorrhoeae viability. EMBO J 19:1098-107

Showing the most recent 10 out of 19 publications