Identification of ALKBH6 as a nucleotide demethylase with a distinct substrate preference

AlkB homolog (ALKBH) family enzymes remove the methyl groups from a variety of substrates including ssDNA and dsDNA, RNA, and proteins. There are eight different ALKBH genes (ALKBH1-8) encoded in the human genome. However, the identity of the substrate of ALKBH6 has remained elusive. In this study, through biochemical experiments and mass spectrometry analysis, we demonstrate that ALKBH6 effectively demethylates N-7-methyl-GMP, and N-1-methyl-adenosine monophosphate. We observed that the presence of a phosphate group in the substrate molecule is essential for ALKBH6 activity as it showed no activity toward methylated bases or the methylated nucleosides. Enzyme kinetic analysis led to the identification of the catalytic and substrate binding residues of ALKBH6 and revealed that succinate and oncometabolite 2-hydroxyglutarate can act as inhibitors of this enzyme. By using mass spectrometry analysis, immunofluorescence microscopy, and ELISA, we confirmed that N-7-methyl-GMP and N-1-methyl-AMP are also the endogenous substrates of ALKBH6. This functional characterization of ALKBH6 broadens the substrate range of ALKBH family proteins and positions ALKBH6 as one of the key players involved in sanitizing the N-methylated nucleotides.

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Journal
Journal of Biological Chemistry
Published
2025-08-28
DOI
https://doi.org/10.1016/j.jbc.2025.110638
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
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article

Identification of ALKBH6 as a nucleotide demethylase with a distinct substrate preference

Sourbh Rankawat, Unnikrishnan Paruthiyezhath Shaji, Sandipan Ray, Nikhil Tuti et al.
1 links
Journal of Biological Chemistry
RNA modifications and cancer
article

Identification of ALKBH6 as a nucleotide demethylase with a distinct substrate preference

Sourbh Rankawat, Unnikrishnan Paruthiyezhath Shaji, Sandipan Ray, Nikhil Tuti, Roy Anindya, Susmita Das, Nafeesa Shahnaz
article en

Abstract

AlkB homolog (ALKBH) family enzymes remove the methyl groups from a variety of substrates including ssDNA and dsDNA, RNA, and proteins. There are eight different ALKBH genes (ALKBH1-8) encoded in the human genome. However, the identity of the substrate of ALKBH6 has remained elusive. In this study, through biochemical experiments and mass spectrometry analysis, we demonstrate that ALKBH6 effectively demethylates N-7-methyl-GMP, and N-1-methyl-adenosine monophosphate. We observed that the presence of a phosphate group in the substrate molecule is essential for ALKBH6 activity as it showed no activity toward methylated bases or the methylated nucleosides. Enzyme kinetic analysis led to the identification of the catalytic and substrate binding residues of ALKBH6 and revealed that succinate and oncometabolite 2-hydroxyglutarate can act as inhibitors of this enzyme. By using mass spectrometry analysis, immunofluorescence microscopy, and ELISA, we confirmed that N-7-methyl-GMP and N-1-methyl-AMP are also the endogenous substrates of ALKBH6. This functional characterization of ALKBH6 broadens the substrate range of ALKBH family proteins and positions ALKBH6 as one of the key players involved in sanitizing the N-methylated nucleotides.

Journal of Biological ChemistryVol. 301(10)
Indian Institute of Technology Hyderabad (IN)
Indian Council of Medical Research, Japan International Cooperation Agency
Zero hunger
Openalex Percentile: Top 80%
RNA modifications and cancer
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