DNA is constantly exposed to endogenous and exogenous agents that produce lesions by modifying its nucleobases. The presence of these lesions in DNA in vivo is associated with aging, diseases such as cancer, and other genetically based diseases. However, DNA damage can also be beneficial. For instance, ionizing radiation is the most common nonsurgical method used to treat cancer. Radiation kills tumor cells by damaging DNA. The goals of this research are to understand how lesions produced in DNA as a result of oxidative stress are repaired, replicated, and react to form other lesions. Our effort is focused on oxidized abasic lesions, which are incapable of forming Watson- Crick hydrogen bonds. Contrary to what was previously believed, oxidized abasic lesions interact with polymerases in distinct ways from each other and from an abasic site (AP) resulting from formal hydrolysis of a nucleotide's glycosidic bond. Hence, the inability to form Watson- Crick hydrogen bonds does not mean that a lesion is noninstructive. We will use synthetic chemistry to synthesize lesions, rapid-quench kinetics to determine polymerase mechanisms, mechanistic studies to determine irreversible inhibition of repair, macromolecular NMR to determine structure, and carry out mutagenesis experiments in yeast to determine the properties of the individual lesions. In addition, we will investigate how oxidized abasic lesions react in nucleosomes. Do nucleosomes affect the reactivity of the lesions? Do they form DNA-protein cross-links? Studies in nucleosomes bring us one step closer to studying DNA damage in cells. We will also design methods for studying DNA repair of abasic sites in cells by using photoacids in conjunction with laser photolysis to produce the lesions. We are also developing modified nucleotides that will be irreversible inhibitors of DNA polymerase b, and important enzyme in base excision repair that is over expressed in tumor cells. In summary, the project combines organic chemistry, biochemistry, and biology with the goal of improving fundamentally important chemical processes that occur in living organisms.
DNA damage and repair are important chemical processes that significantly impact human health. These chemical processes are associated with aging and a variety of diseases, such as cancer. Understanding the chemistry, biochemistry, and biological effects of damaged DNA enhances our molecular level understanding of the etiology of diseases, such as cancer, as well as the various treatments for which nucleic acids are the target.
|Ghosh, Souradyuti; Greenberg, Marc M (2014) Nucleotide excision repair of chemically stabilized analogues of DNA interstrand cross-links produced from oxidized abasic sites. Biochemistry 53:5958-65|
|Greenberg, Marc M (2014) Looking beneath the surface to determine what makes DNA damage deleterious. Curr Opin Chem Biol 21:48-55|
|Cunniffe, Siobhan; O'Neill, Peter; Greenberg, Marc M et al. (2014) Reduced repair capacity of a DNA clustered damage site comprised of 8-oxo-7,8-dihydro-2'-deoxyguanosine and 2-deoxyribonolactone results in an increased mutagenic potential of these lesions. Mutat Res 762:32-9|
|Arian, Dumitru; Hedayati, Mohammad; Zhou, Haoming et al. (2014) Irreversible inhibition of DNA polymerase ? by small-molecule mimics of a DNA lesion. J Am Chem Soc 136:3176-83|
|Ghosh, Souradyuti; Greenberg, Marc M (2014) Synthesis of cross-linked DNA containing oxidized abasic site analogues. J Org Chem 79:5948-57|
|Greenberg, Marc M (2014) Abasic and oxidized abasic site reactivity in DNA: enzyme inhibition, cross-linking, and nucleosome catalyzed reactions. Acc Chem Res 47:646-55|
|Bajacan, John Ernest V; Greenberg, Marc M (2013) DNA polymerase V kinetics support the instructive nature of an oxidized abasic lesion in Escherichia coli. Biochemistry 52:6301-3|
|Crespan, Emmanuele; Pasi, Emanuela; Imoto, Shuhei et al. (2013) Human DNA polymerase ýý, but not ýý, can bypass a 2-deoxyribonolactone lesion together with proliferating cell nuclear antigen. ACS Chem Biol 8:336-44|
|Zhou, Chuanzheng; Sczepanski, Jonathan T; Greenberg, Marc M (2013) Histone modification via rapid cleavage of C4'-oxidized abasic sites in nucleosome core particles. J Am Chem Soc 135:5274-7|
|Sczepanski, Jonathan T; Zhou, Chuanzheng; Greenberg, Marc M (2013) Nucleosome core particle-catalyzed strand scission at abasic sites. Biochemistry 52:2157-64|
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