Cancer and bacterial infections are caused by uncontrolled multiplication of undesired cell types within the organism. Effective treatments target critical and specific parts of these undesired cells, absent in by-stander cells of the organism. One successful strategy to fight cancer or infections is to target the complex DNA metabolism of the undesired cells, causing their chromosomal death, ? a mysterious phenomenon, whose mechanisms are still completely unclear. Chromosomal death is the inability to continue chromosome cycle ?the cycle of replication and segregation of genetic information that drives the cell cycle. The chromosomal cycle is blocked by chromosomal lesions ? DNA lesions that are so complex and harmful, that they inactivate the entire chromosomes. A classic chromosomal lesion is a double-strand DNA break, but the most common chromosomal lesions are efficiently mended by pathways of recombinational repair and various back-ups. We are purposefully looking for and characterizing conditions that induce irreparable chromosomal lesions that cause chromosomal death, to make it possible to convert them into future treatments against undesirable cells. This application describes our characterization of two such conditions: (i) thymine starvation; (ii) toxic RNA incorporation into DNA. In characterizing a chromosome- associated lethal phenomenon, we practice a three-pronged approach. On the one hand, we identify the most dramatic physical readouts; on the other hand, we identify the most interesting phenotypes of mutants. The third arm of the analysis is to look at the chromosome from the genome perspective. Our fist specific aim will address genetic and metabolic aspects of thymine starvation in relation to its three distinct phases. The second specific aim will characterize physical changes in the chromosome during thymine starvation.
The third aim i s about comprehensive characterization of the novel phenomenon of the unexpected RNA nucleotide toxicity within the chromosomal DNA. Combining the most relevant physical readouts with the most interesting mutants and the most dramatic genomic patterns should yield a comprehensive 3D-picture of the phenomenon in genetic / physical / genomic dimensions, producing mechanistic insights into the most complicated mechanisms of chromosomal death.

Public Health Relevance

Compared to exogenous DNA damage, which usefulness is limited by toxicity to by-stander cells, cell-type-specific induction of endogenous DNA damage is a much safer approach to effect chromosomal death in undesirable cell types without affecting by-standers. This research program investigates how inhibition of two specific segments of the DNA replication metabolism causes chromosomal death in bacteria. The obtained information will lay a foundation for future design of highly-specific and potent anti-cancer and anti-infection treatments.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM073115-10A1
Application #
9660926
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Willis, Kristine Amalee
Project Start
2007-06-01
Project End
2022-12-31
Budget Start
2019-01-01
Budget End
2019-12-31
Support Year
10
Fiscal Year
2019
Total Cost
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
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; 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
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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