Role of Tet1 and 5-hydroxymethylcytosine in cocaine action.

TitleRole of Tet1 and 5-hydroxymethylcytosine in cocaine action.
Publication TypeJournal Article
Year of Publication2015
AuthorsFeng J, Shao N, Szulwach KE, Vialou V, Huynh J, Zhong C, Le T, Ferguson D, Cahill ME, Li Y, Koo JWook, Ribeiro E, Labonte B, Laitman BM, Estey D, Stockman V, Kennedy P, Couroussé T, Mensah I, Turecki G, Faull KF, Ming G-li, Song H, Fan G, Casaccia P, Shen L, Jin P, Nestler EJ
JournalNat Neurosci
Volume18
Issue4
Pagination536-44
Date Published2015 Apr
ISSN1546-1726
KeywordsAnimals, Behavior, Animal, Cocaine, Cytosine, DNA-Binding Proteins, Down-Regulation, Epigenesis, Genetic, Gene Expression, Male, Mice, Mice, Inbred C57BL, Nucleus Accumbens, Proto-Oncogene Proteins
Abstract

Ten-eleven translocation (TET) enzymes mediate the conversion of 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC), which is enriched in brain, and its ultimate DNA demethylation. However, the influence of TET and 5hmC on gene transcription in brain remains elusive. We found that ten-eleven translocation protein 1 (TET1) was downregulated in mouse nucleus accumbens (NAc), a key brain reward structure, by repeated cocaine administration, which enhanced behavioral responses to cocaine. We then identified 5hmC induction in putative enhancers and coding regions of genes that have pivotal roles in drug addiction. Such induction of 5hmC, which occurred similarly following TET1 knockdown alone, correlated with increased expression of these genes as well as with their alternative splicing in response to cocaine administration. In addition, 5hmC alterations at certain loci persisted for at least 1 month after cocaine exposure. Together, these reveal a previously unknown epigenetic mechanism of cocaine action and provide new insight into how 5hmC regulates transcription in brain in vivo.

DOI10.1038/nn.3976
Alternate JournalNat. Neurosci.
PubMed ID25774451
PubMed Central IDPMC4617315
Grant ListP01 DA008227 / DA / NIDA NIH HHS / United States
R01 DA007359 / DA / NIDA NIH HHS / United States
R37 NS042925 / NS / NINDS NIH HHS / United States

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