Role of DNA polymerase β oxidized nucleotide insertion in DNA ligation failure. (11th July 2017)

• Record Type: Journal Article
• Authors: Çağlayan, Melike; Wilson, Samuel H
• Is Part Of: Journal of radiation research. Volume 58:Number 5(2017:Sep.)
• Page Start: 603
• Page End: 607
• Publication Date: 2017-07-11
• Subjects: genome stability -- oxidative DNA damage -- base excision repair -- DNA polymerase β -- DNA ligase I; Radiology, Medical -- Periodicals; Radiobiology -- Periodicals; Radiation -- Periodicals; 616.0757
• DOI: 10.1093/jrr/rrx027
• Languages: English
• ISSNs: 0449-3060

Abstract

Abstract: Production of reactive oxygen and nitrogen species (ROS), such as hydrogen peroxide, superoxide and hydroxyl radicals, has been linked to cancer, and these oxidative molecules can damage DNA. Base excision repair (BER), a major repair system maintaining genome stability over a lifespan, has an important role in repairing oxidatively induced DNA damage. Failure of BER leads to toxic consequences in ROS-exposed cells, and ultimately can contribute to the pathobiology of disease. In our previous report, we demonstrated that oxidized nucleotide insertion by DNA polymerase β (pol β) impairs BER due to ligation failure and leads to formation of a cytotoxic repair intermediate. Biochemical and cytotoxic effects of ligation failure could mediate genome stability and influence cancer therapeutics. In this review, we discuss the importance of coordination between pol β and DNA ligase I during BER, and how this could be a fundamental mechanism underlying human diseases such as cancer and neurodegeneration. A summary of this work was presented in a symposium at the International Congress of Radiation Research 2015 in Kyoto, Japan.