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MutY-glycosylase: An overview on mutagenesis and activities beyond the GO system

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.mrfmmm.2014.08.002

Keywords

MutY-glycosylase; DNA damage; DNA repair; GO system; Mutagenesis; Oxidative stress

Funding

  1. Programa Nacional de Cooperacao Academica da Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior - CAPES/Brazil [PROCAD-NF: 23038001273/2010-20]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) (Bolsa de Pos Doutorado - PDJ) [164160/2013-2]
  3. INCT-Redox Processes in Biomedicine, Redoxome - CNPq [573530/2008-4]
  4. Fundacao de Amparo a Pesquisa do Rio Grande do Sul (FAPERGS) (Pronex - Fapergs/CNPq and PqG) [10/0044-3, 06/2010]
  5. GENOTOX-Genotoxicity Laboratory - Royal Institute

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MutY is a glycosylase known for its role in DNA base excision repair (BER). It is critically important in the prevention of DNA mutations derived from 7,8-dihydro-8-oxoguanine (8-oxoG), which are the major lesions resulting from guanine oxidation. MutY has been described as a DNA repair enzyme in the GO system responsible for removing adenine residues misincorporated in 8-oxoG:A mispairs, avoiding G:C to T:A mutations. Further studies have shown that this enzyme binds to other mispairs, interacts with several enzymes, avoids different transversions/transitions in DNA, and is involved in different repair pathways. Additional activities have been reported for MutY, such as the repair of replication errors in newly synthesized DNA strands through its glycosylase activity. Moreover, MutY is a highly conserved enzyme present in several prokaryotic and eukaryotic organisms. MutY defects are associated with a hereditary colorectal cancer syndrome termed MUTYH-associated polyposis (MAP). Here, we have reviewed the roles of MutY in the repair of mispaired bases in DNA as well as its activities beyond the GO system. (C) 2014 Elsevier B.V. All rights reserved.

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