Specificity of stimulation of human 8-oxoguanine-DNA glycosylase by AP endonuclease |
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| Authors: | Sidorenko Viktoriya S Nevinsky Georgy A Zharkov Dmitry O |
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| Institution: | a SB RAS Institute of Chemical Biology and Fundamental Medicine, Laboratory of Repair Enzymes, 8 Lavrentieva Avenue, Novosibirsk 630090, Russia
b Department of Natural Sciences, Novosibirsk State University, Novosibirsk 630090, Russia |
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| Abstract: | Human 8-oxoguanine-DNA glycosylase OGG1 is an enzyme that removes abundant oxidative lesion 8-oxoguanine (8-oxoG) from DNA. Excision of 8-oxoG by OGG1 is inhibited by the abasic DNA reaction product and is stimulated by AP endonuclease APEX1. Besides 8-oxoG, OGG1 shows activity towards several other base lesions. Here we report that APEX1 efficiently stimulates OGG1 on good substrates (8-oxoadenine, 8-oxoinosine, or 6-methoxy-8-oxoguanine opposite to cytosine) but the stimulation is low or absent with poor OGG1 substrates (8-oxoadenine or 8-oxoinosine opposite to thymine; 8-oxoG or 8-aminoguanine opposite to adenine; 8-oxonebularine, 8-metoxyguanine, inosine or guanine opposite to cytosine). APEX1 significantly improves the ability of OGG1 to excise 8-aminoguanine from its naturally occurring pair with cytosine, making it possible that OGG1 repairs this lesion. Overall, APEX1 serves to improve specificity of OGG1 for its biologically relevant substrates. |
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| Keywords: | DNA repair 8-oxoguanine-DNA glycosylase AP endonuclease Protein-protein interactions |
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