Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Aug;50(3):2477-2491.
doi: 10.1111/ejn.14170. Epub 2018 Oct 10.

It is a complex issue: emerging connections between epigenetic regulators in drug addiction

Affiliations
Review

It is a complex issue: emerging connections between epigenetic regulators in drug addiction

Ethan M Anderson et al. Eur J Neurosci. 2019 Aug.

Abstract

Drug use leads to addiction in some individuals, but the underlying brain mechanisms that control the transition from casual drug use to an intractable substance use disorder (SUD) are not well understood. Gene x environment interactions such as the frequency of drug use and the type of substance used likely to promote maladaptive plastic changes in brain regions that are critical for controlling addiction-related behavior. Epigenetics encompasses a broad spectrum of mechanisms important for regulating gene transcription that are not dependent on changes in DNA base pair sequences. This review focuses on the proteins and complexes contributing to epigenetic modifications in the nucleus accumbens (NAc) following drug experience. We discuss in detail the three major mechanisms: histone acetylation and deacetylation, histone methylation, and DNA methylation. We discuss how drug use alters the regulation of the associated proteins regulating these processes and highlight how experimental manipulations of these proteins in the NAc can alter drug-related behaviors. Finally, we discuss the ways that histone modifications and DNA methylation coordinate actions by recruiting large epigenetic enzyme complexes to aid in transcriptional repression. Targeting these multiprotein epigenetic enzyme complexes - and the individual proteins that comprise them - might lead to effective therapeutics to reverse or treat SUDs in patients.

Keywords: DNMT; G9a; HDAC; MeCP2; substance use disorder.

PubMed Disclaimer

References

    1. Ago, T., Liu, T., Zhai, P., Chen, W., Li, H., Molkentin, J.D., Vatner, S.F. & Sadoshima, J. (2008) A redox-dependent pathway for regulating class II HDACs and cardiac hypertrophy. Cell, 133, 978-993.
    1. Aguilar-Valles, A., Vaissiere, T., Griggs, E.M., Mikaelsson, M.A., Takacs, I.F., Young, E.J., Rumbaugh, G. & Miller, C.A. (2014) Methamphetamine-associated memory is regulated by a writer and an eraser of permissive histone methylation. Biol. Psychiat., 76, 57-65.
    1. Allfrey, V.G., Faulkner, R. & Mirsky, A.E. (1964) Acetylation and methylation of histones and their possible role in the regulation of RNA synthesis. Proc. Natl Acad. Sci. USA, 51, 786-794.
    1. Allis, C.D. & Jenuwein, T. (2016) The molecular hallmarks of epigenetic control. Nat. Rev. Genet., 17, 487-500.
    1. Allis, C.D., Berger, S.L., Cote, J., Dent, S., Jenuwien, T., Kouzarides, T., Pillus, L., Reinberg, D. et al. (2007) New nomenclature for chromatin-modifying enzymes. Cell, 131, 633-636.

Publication types

MeSH terms