The use of base analogs as effective antivirals, antimicrobials and anti-cancer agents is limited by their toxicity to the host organism. This toxicity is attributed to either poisoning of the regular nucleotide metabolism by inhibiting key enzymes or to hypermutagenesis. We have recently demonstrated that even natural base analogs uracil and hypoxanthine, that are not known to elicit any of the above consequences, are still genotoxic in E. coli because they induce chromosomal fragmentation. It turns out that chromosomal fragmentation is an important, though often ignored, consequence of the nucleotide pool imbalance and contamination with non-canonical DNA precursors. We propose to investigate the chromosomal consequences of nucleotide pool imbalance and contamination in the rdgB, dut, tdk and thyA mutants of E. coli guided by the following questions: 1) what are the modified DNA precursors in the nucleotide pools and modified bases in DNA? 2) What are the pathways of the modified DNA precursor synthesis and modified base repair? 3) What are the mechanisms of chromosomal fragmentation, caused by incorporation of the modified bases into DNA? To this end, we will use the following methods: 2-dimensional thin layer chromatography to detect modified DNA precursors, enzymatic excision with subsequent post-labeling to identify modified nucleotides in DNA;isolation of mutants synthetic lethal with the rdgB, tdk and dut genes to reveal cause-consequence-correction interactions between seemingly unlinked metabolic pathways;isolation of suppressors of synthetic lethalities with rdgB, tdk and dut inactivations to reveal the mechanisms behind the synthetic lethalities;determination of mutation spectra of the rdgB, tdk and dut mutants;pulsed-field gel electrophoresis to study mechanisms of the chromosomal fragmentation in these mutants. The proposed research will lead to a better understanding of the clastogenic potential of base analogs, as well as to elucidation of the chromosomal breakage-avoidance strategies of the cell.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM073115-02S1
Application #
7921262
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Portnoy, Matthew
Project Start
2009-09-30
Project End
2011-08-31
Budget Start
2009-09-30
Budget End
2011-08-31
Support Year
2
Fiscal Year
2009
Total Cost
$125,285
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Microbiology/Immun/Virology
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Kuzminov, Andrei (2018) When DNA Topology Turns Deadly - RNA Polymerases Dig in Their R-Loops to Stand Their Ground: New Positive and Negative (Super)Twists in the Replication-Transcription Conflict. Trends Genet 34:111-120
Khan, Sharik R; Kuzminov, Andrei (2017) Degradation of RNA during lysis of Escherichia coli cells in agarose plugs breaks the chromosome. PLoS One 12:e0190177
Khan, Sharik R; Kuzminov, Andrei (2017) Pulsed-field gel electrophoresis does not break E. coli chromosome undergoing excision repair after UV irradiation. Anal Biochem 526:66-68
Mahaseth, Tulip; Kuzminov, Andrei (2017) Potentiation of hydrogen peroxide toxicity: From catalase inhibition to stable DNA-iron complexes. Mutat Res 773:274-281
Kouzminova, Elena A; Kadyrov, Farid F; Kuzminov, Andrei (2017) RNase HII Saves rnhA Mutant Escherichia coli from R-Loop-Associated Chromosomal Fragmentation. J Mol Biol 429:2873-2894
Khan, Sharik R; Mahaseth, Tulip; Kouzminova, Elena A et al. (2016) Static and Dynamic Factors Limit Chromosomal Replication Complexity in Escherichia coli, Avoiding Dangers of Runaway Overreplication. Genetics 202:945-60
Kuzminov, Andrei (2016) Chromosomal Replication Complexity: A Novel DNA Metrics and Genome Instability Factor. PLoS Genet 12:e1006229
Mahaseth, Tulip; Kuzminov, Andrei (2016) Prompt repair of hydrogen peroxide-induced DNA lesions prevents catastrophic chromosomal fragmentation. DNA Repair (Amst) 41:42-53
Mahaseth, Tulip; Kuzminov, Andrei (2015) Cyanide enhances hydrogen peroxide toxicity by recruiting endogenous iron to trigger catastrophic chromosomal fragmentation. Mol Microbiol 96:349-67
Rotman, Ella; Khan, Sharik R; Kouzminova, Elena et al. (2014) Replication fork inhibition in seqA mutants of Escherichia coli triggers replication fork breakage. Mol Microbiol 93:50-64

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