Control of histone demethylation by nuclear-localized α-ketoglutarate dehydrogenase

Science. 2023 Jul 14;381(6654):eadf8822. doi: 10.1126/science.adf8822. Epub 2023 Jul 14.

Abstract

Methylations on nucleosomal histones play fundamental roles in regulating eukaryotic transcription. Jumonji C domain-containing histone demethylases (JMJs) dynamically control the level of histone methylations. However, how JMJ activity is generally regulated is unknown. We found that the tricarboxylic acid cycle-associated enzyme α-ketoglutarate (α-KG) dehydrogenase (KGDH) entered the nucleus, where it interacted with various JMJs to regulate α-KG-dependent histone demethylations by JMJs, and thus controlled genome-wide gene expression in plants. We show that nuclear targeting is regulated by environmental signals and that KGDH is enriched at thousands of loci in Arabidopsis thaliana. Chromatin-bound KGDH catalyzes α-KG decarboxylation and thus may limit its local availability to KGDH-coupled JMJs, inhibiting histone demethylation. Thus, our results uncover a regulatory mechanism for histone demethylations by JMJs.

MeSH terms

  • Arabidopsis Proteins* / genetics
  • Arabidopsis Proteins* / metabolism
  • Arabidopsis* / enzymology
  • Arabidopsis* / genetics
  • Cell Nucleus / enzymology
  • Chromatin / metabolism
  • Demethylation
  • Gene Expression Regulation, Plant
  • Histone Demethylases / genetics
  • Histones* / metabolism
  • Jumonji Domain-Containing Histone Demethylases* / genetics
  • Ketoglutarate Dehydrogenase Complex* / genetics
  • Ketoglutarate Dehydrogenase Complex* / metabolism

Substances

  • Arabidopsis Proteins
  • Chromatin
  • Histone Demethylases
  • Histones
  • Jumonji Domain-Containing Histone Demethylases
  • Ketoglutarate Dehydrogenase Complex