4.6 Article

Oxidative demethylase ALKBH5 repairs DNA alkylation damage and protects against alkylation-induced toxicity

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2020.12.017

Keywords

AlkB; ALKBH2; ALKBH3; ALKBH5; DNA repair; Demethylation; Fe(II)/20G-Dependent dioxygenase; N3-methylcytosine; DNA alkylation; Alkyl adducts

Funding

  1. Science and Engineering Research Board (SERB) [EMR/2016/005135/BBM]

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ALKBH5, known as a RNA N6-methyladenine demethylase, is also found to have weak DNA repair activity and can demethylate DNA 3-methylcytosine. Overexpression of ALKBH5 reduces the level of 3-methylcytosine in genomic DNA and decreases the cytotoxic effects of the DNA damaging alkylating agent. This suggests that demethylation by ALKBH5 may play a supporting role in maintaining genome integrity.
DNA integrity is challenged by both exogenous and endogenous alkylating agents. DNA repair proteins such as Escherichia coli AIkB family of enzymes can repair 1-methyladenine and 3-methylcytosine adducts by oxidative demethylation. Human AIkB homologue 5 (ALKBH5) is RNA N6-methyladenine demethylase and not known to be involved in DNA repair. Herein we show that ALKBH5 also has weak DNA repair activity and it can demethylate DNA 3-methylcytosine. The mutation of the amino acid residues involved in demethylation also abolishes the DNA repair activity of ALKBH5. Overexpression of ALKBH5 decreases the 3-methylcytosine level in genomic DNA and reduces the cytotoxic effects of the DNA damaging alkylating agent methyl methanesulfonate. Thus, demethylation by ALKBH5 might play a supporting role in maintaining genome integrity. (C) 2020 Elsevier Inc. All rights reserved.

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