REVIEW: Role of Nucleotide Excision Repair Proteins in Oxidative DNA Damage Repair: an Updating

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B. Pascucci^1,2, M. D’Errico², E. Parlanti², S. Giovannini², and E. Dogliotti²*

¹Istituto di Cristallografia, Consiglio Nazionale delle Ricerche, Via Salaria Km 29.300, 00016 Monterotondo Stazione, Rome, Italy; fax: +3(906)9067-2630; E-mail: barbara.pascucci@mlib.ic.cnr.it

²Department of Environment and Primary Prevention, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy; fax: +3(906)4990-3650; E-mail: mariarosaria.derrico@iss.it; eleonora.parlanti@iss.it; giovannini.sara@hotmail.it; eugenia.dogliotti@iss.it

^* To whom correspondence should be addressed.

Received September 15, 2010; Revision received October 8, 2010

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DNA repair is a crucial factor in maintaining a low steady-state level of oxidative DNA damage. Base excision repair (BER) has an important role in preventing the deleterious effects of oxidative DNA damage, but recent evidence points to the involvement of several repair pathways in this process. Oxidative damage may arise from endogenous and exogenous sources and may target nuclear and mitochondrial DNA as well as RNA and proteins. The importance of preventing mutations associated with oxidative damage is shown by a direct association between defects in BER (i.e. MYH DNA glycosylase) and colorectal cancer, but it is becoming increasingly evident that damage by highly reactive oxygen species plays also central roles in aging and neurodegeneration. Mutations in genes of the nucleotide excision repair (NER) pathway are associated with diseases, such as xeroderma pigmentosum and Cockayne syndrome, that involve increased skin cancer and/or developmental and neurological symptoms. In this review we will provide an updating of the current evidence on the involvement of NER factors in the control of oxidative DNA damage and will attempt to address the issue of whether this unexpected role may unlock the difficult puzzle of the pathogenesis of these syndromes.

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KEY WORDS: oxidative damage, DNA repair, oxidative metabolism, xeroderma pigmentosum, Cockayne syndrome

DOI: 10.1134/S0006297911010032

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