» Articles » PMID: 25562692

Metabolic Regulation of Histone Post-translational Modifications

Overview
Journal ACS Chem Biol
Specialties Biochemistry
Biology
Date 2015 Jan 7
PMID 25562692
Citations 151
Authors
Affiliations
Soon will be listed here.
Abstract

Histone post-translational modifications regulate transcription and other DNA-templated functions. This process is dynamically regulated by specific modifying enzymes whose activities require metabolites that either serve as cosubstrates or act as activators/inhibitors. Therefore, metabolism can influence histone modification by changing local concentrations of key metabolites. Physiologically, the epigenetic response to metabolism is important for nutrient sensing and environment adaption. In pathologic states, the connection between metabolism and histone modification mediates epigenetic abnormality in complex disease. In this review, we summarize recent studies of the molecular mechanisms involved in metabolic regulation of histone modifications and discuss their biological significance.

Citing Articles

Examining the epigenetic transmission of risk for chronic pain associated with paternal post-traumatic stress disorder: a focus on veteran populations.

Freeman J, Salberg S, Noel M, Mychasiuk R Transl Psychiatry. 2025; 15(1):42.

PMID: 39910041 PMC: 11799465. DOI: 10.1038/s41398-025-03267-w.


Mitochondria and its epigenetic dynamics: Insight into synaptic regulation and synaptopathies.

Gupta S, Kishore A, Rishi V, Aggarwal A Funct Integr Genomics. 2025; 25(1):26.

PMID: 39849126 DOI: 10.1007/s10142-025-01530-3.


High-Fat Diet, Epigenetics, and Atherosclerosis: A Narrative Review.

Rai V Nutrients. 2025; 17(1.

PMID: 39796562 PMC: 11722563. DOI: 10.3390/nu17010127.


Bidirectional histone monoaminylation dynamics regulate neural rhythmicity.

Zheng Q, Weekley B, Vinson D, Zhao S, Bastle R, Thompson R Nature. 2025; 637(8047):974-982.

PMID: 39779849 PMC: 11754111. DOI: 10.1038/s41586-024-08371-3.


Mitochondria: the epigenetic regulators of ovarian aging and longevity.

Mani S, Srivastava V, Shandilya C, Kaushik A, Singh K Front Endocrinol (Lausanne). 2024; 15:1424826.

PMID: 39605943 PMC: 11598335. DOI: 10.3389/fendo.2024.1424826.


References
1.
Shimazu T, Hirschey M, Newman J, He W, Shirakawa K, Le Moan N . Suppression of oxidative stress by β-hydroxybutyrate, an endogenous histone deacetylase inhibitor. Science. 2012; 339(6116):211-4. PMC: 3735349. DOI: 10.1126/science.1227166. View

2.
Lee J, Carrer A, Shah S, Snyder N, Wei S, Venneti S . Akt-dependent metabolic reprogramming regulates tumor cell histone acetylation. Cell Metab. 2014; 20(2):306-319. PMC: 4151270. DOI: 10.1016/j.cmet.2014.06.004. View

3.
Luger K, Mader A, Richmond R, Sargent D, Richmond T . Crystal structure of the nucleosome core particle at 2.8 A resolution. Nature. 1997; 389(6648):251-60. DOI: 10.1038/38444. View

4.
Preiss J, Handler P . Biosynthesis of diphosphopyridine nucleotide. I. Identification of intermediates. J Biol Chem. 1958; 233(2):488-92. View

5.
Karch K, DeNizio J, Black B, Garcia B . Identification and interrogation of combinatorial histone modifications. Front Genet. 2014; 4:264. PMC: 3868920. DOI: 10.3389/fgene.2013.00264. View