JmjC Histone Demethylases: Beyond Histone Lysine Demethylation

Authors

  • Joanna Bonnici Chemistry – School of Natural & Environmental Sciences, Newcastle University, Newcastle NE1 7RU, UK https://orcid.org/0000-0002-2723-6895
  • Christopher J. Schofield Department of Chemistry, University of Oxford, OX1 3TA, UK https://orcid.org/0000-0002-0290-6565
  • Akane Kawamura Chemistry – School of Natural & Environmental Sciences, Newcastle University, Newcastle NE1 7RU, UK; Department of Chemistry, University of Oxford, OX1 3TA, UK

DOI:

https://doi.org/10.2533/chimia.2026.138

Keywords:

Argine demethylation / hydroxylation, Cancer metabolism, Epigenetics, JmjC histone demethylases, JmjC-KDMs, 2-oxoglutarate (2OG) dependent oxygenases

Abstract

Jumonji C histone lysine demethylases (JmjC-KDMs) are key chromatin regulators best known for catalysing histone lysine demethylation. There is growing evidence that JmjC-KDMs have a broader catalytic scope. This review summarises recent advances on JmjC-KDM activities beyond histone lysine demethylation, including arginine demethylation and arginine hydroxylation. We discuss how emerging insights into sequence-reactivity and inter-domain relationships, combinatorial post-translational modifications (PTMs), and cellular context shape substrate selectivity and enzymatic outcomes. These findings highlight substantial mechanistic flexibility within the JmjC-KDM family and may help prompt reconsideration of how their biochemistry is connected to physiological roles. We discuss implications for JmjC-KDM inhibitor development and outline outstanding questions, guiding future research concerning their roles in epigenetic regulation.

Funding data

Author Biography

  • Christopher J. Schofield, Department of Chemistry, University of Oxford, OX1 3TA, UK

    Professor of Chemistry

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Published

2026-03-25

How to Cite

[1]
J. Bonnici, C. J. Schofield, A. Kawamura, Chimia 2026, 80, 138, DOI: 10.2533/chimia.2026.138.