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

DNA integrity is challenged by both exogenous and endogenous alkylating agents. DNA repair proteins such as Escherichia coli AlkB family of enzymes can repair 1-methyladenine and 3-methylcytosine adducts by oxidative demethylation. Human AlkB homologue 5 (ALKBH5) is RNA N6-methyladenine demethylase...

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Veröffentlicht in:Biochemical and biophysical research communications 2021-01, Vol.534, p.114-120
Hauptverfasser: Akula, Deepa, O’Connor, Timothy R., Anindya, Roy
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Sprache:eng
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Zusammenfassung:DNA integrity is challenged by both exogenous and endogenous alkylating agents. DNA repair proteins such as Escherichia coli AlkB family of enzymes can repair 1-methyladenine and 3-methylcytosine adducts by oxidative demethylation. Human AlkB 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. •Fe(II)/2OG-dependent dioxygenase ALKBH5 can demethylate 3meC in vitro.•ALKBH5 rescues MMS sensitivity in heterologous system.•ALKBH5 overexpression can demethylate 3meC from genomic DNA in vivo.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2020.12.017