Our genome is continuously damaged by environmental, endogenous agents as well as by the instrinsic instability of DNA. For example, UV light gives rise to helix-distorting cyclobutane pyrimidine dimers (CPDs) and pyrimidine-(6,4)-pyrimidone adducts (6-4PPs). Ionizing radiation can cause both single and double strand breaks in DNA and numerous types of oxidative lesions. Chemotherapeutics, that are used in cancer therapy, and other environmental chemical agents, which are present in e.g. polluted air and tobacco smoke, induce a plethora of DNA lesions, including intra- and inter-strand cross-links and mono-adducts. In addition, endogenous agents cause a wide variety of DNA lesions. Metabolic processes within our cells lead to reactive oxygen species (ROS), which react with proteins, lipids and DNA. Although ROS participate in beneficial physiological processes as growth factor signal transduction, these by-products of metabolism also underlie a broad spectrum of oxidative DNA lesions, including 8-oxo-2’-deoxyguanosine (8-oxodG), thymine glycols, cylcopurines, as well as single and double strand breaks. Finally, lesions in the DNA can also form without a direct damaging agent. E.g. spontaneous hydrolysis or modifications of nucleotides occurs in cells, which leaves non-informative a-basic sites or altered, miscoding nucleotides.

Additional Metadata
Keywords DNA damage, DNA repair, bone aging, mice, trichothiodystrophy
Promotor Leeuwen, J.P.T.M. van (Hans) , Hoeijmakers, J.H.J. (Jan) , Horst, G.T.J. van der (Gijsbertus)
Publisher Erasmus University Rotterdam
Sponsor Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO), Research Institute for Diseases of the Elderly, National Institute of Health, National Institute of Environmental Health Sciences, Konigin Wilhelmina Fonds (KWF), EU
ISBN 978-908559-915-9
Persistent URL hdl.handle.net/1765/17723
Citation
Diderich, K.. (2010, January 6). Bone Aging in DNA Repair Deficient Trichothiodystrophy Mice. Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/17723