TY - JOUR
T1 - Prefrontal cortex expression of chromatin modifier genes in male WSP and WSR mice changes across ethanol dependence, withdrawal, and abstinence
AU - Hashimoto, Joel G.
AU - Gavin, David P.
AU - Wiren, Kristine M.
AU - Crabbe, John C.
AU - Guizzetti, Marina
N1 - Funding Information:
This work was supported by the Department of Veterans Affairs: Merit Review Awards I01 BX001819 (M.G.) and Career Development Award (CDA-2) IK2BX001650 (D.P.G.); National Institutes of Health: R01AA021468, R21AA021876, and R01AA022948 (M.G.), and NARSAD Young Investigator Award donation from The Family of Joseph M. Evans (D.P.G.). We also acknowledge support from VA Merit Review grant 101BX000313, and NIH grants U01 AA013519, P60 AA10760, and R24 AA020245 for the production and maintenance of WSP and WSR mouse colonies and for the use of ethanol vapor chambers. The authors have no conflicts of interest to disclose. We thank Dr. Pamela Metten for critically reading the manuscript.
Publisher Copyright:
© 2017
PY - 2017/5/1
Y1 - 2017/5/1
N2 - Alcohol-use disorder (AUD) is a relapsing disorder associated with excessive ethanol consumption. Recent studies support the involvement of epigenetic mechanisms in the development of AUD. Studies carried out so far have focused on a few specific epigenetic modifications. The goal of this project was to investigate gene expression changes of epigenetic regulators that mediate a broad array of chromatin modifications after chronic alcohol exposure, chronic alcohol exposure followed by 8 h withdrawal, and chronic alcohol exposure followed by 21 days of abstinence in Withdrawal-Resistant (WSR) and Withdrawal Seizure-Prone (WSP) selected mouse lines. We found that chronic vapor exposure to highly intoxicating levels of ethanol alters the expression of several chromatin remodeling genes measured by quantitative PCR array analyses. The identified effects were independent of selected lines, which, however, displayed baseline differences in epigenetic gene expression. We reported dysregulation in the expression of genes involved in histone acetylation, deacetylation, lysine and arginine methylation and ubiquitinationhylation during chronic ethanol exposure and withdrawal, but not after 21 days of abstinence. Ethanol-induced changes are consistent with decreased histone acetylation and with decreased deposition of the permissive ubiquitination mark H2BK120ub, associated with reduced transcription. On the other hand, ethanol-induced changes in the expression of genes involved in histone lysine methylation are consistent with increased transcription. The net result of these modifications on gene expression is likely to depend on the combination of the specific histone tail modifications present at a given time on a given promoter. Since alcohol does not modulate gene expression unidirectionally, it is not surprising that alcohol does not unidirectionally alter chromatin structure toward a closed or open state, as suggested by the results of this study.
AB - Alcohol-use disorder (AUD) is a relapsing disorder associated with excessive ethanol consumption. Recent studies support the involvement of epigenetic mechanisms in the development of AUD. Studies carried out so far have focused on a few specific epigenetic modifications. The goal of this project was to investigate gene expression changes of epigenetic regulators that mediate a broad array of chromatin modifications after chronic alcohol exposure, chronic alcohol exposure followed by 8 h withdrawal, and chronic alcohol exposure followed by 21 days of abstinence in Withdrawal-Resistant (WSR) and Withdrawal Seizure-Prone (WSP) selected mouse lines. We found that chronic vapor exposure to highly intoxicating levels of ethanol alters the expression of several chromatin remodeling genes measured by quantitative PCR array analyses. The identified effects were independent of selected lines, which, however, displayed baseline differences in epigenetic gene expression. We reported dysregulation in the expression of genes involved in histone acetylation, deacetylation, lysine and arginine methylation and ubiquitinationhylation during chronic ethanol exposure and withdrawal, but not after 21 days of abstinence. Ethanol-induced changes are consistent with decreased histone acetylation and with decreased deposition of the permissive ubiquitination mark H2BK120ub, associated with reduced transcription. On the other hand, ethanol-induced changes in the expression of genes involved in histone lysine methylation are consistent with increased transcription. The net result of these modifications on gene expression is likely to depend on the combination of the specific histone tail modifications present at a given time on a given promoter. Since alcohol does not modulate gene expression unidirectionally, it is not surprising that alcohol does not unidirectionally alter chromatin structure toward a closed or open state, as suggested by the results of this study.
KW - Alcohol-use disorder
KW - DNA methylation
KW - Epigenetics
KW - Histone acetylation
KW - Histone arginine acetylation
KW - Histone lysine methylation
KW - Histone ubiquitination
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U2 - 10.1016/j.alcohol.2017.01.010
DO - 10.1016/j.alcohol.2017.01.010
M3 - Article
C2 - 28433423
AN - SCOPUS:85017511574
SN - 0741-8329
VL - 60
SP - 83
EP - 94
JO - Alcohol
JF - Alcohol
ER -