Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. Locus-specific epigenetic remodeling controls addiction- and depression-related behaviors

Locus-specific epigenetic remodeling controls addiction- and depression-related behaviors

Thumbnail Image
Download
Name

Zhang_Locus-specific.pdf

Size

1.21 MB

Format

Adobe PDF

Checksum (MD5)

fd4b96dba5dc014a77d01d64b92f0fb3

Author(s)
Sun, Haosheng
•
Shao, Ningyi
•
Feng, Jian
•
Mazei-Robison, Michelle
•
Ferguson, Deveroux
•
Knight, Scott
•
Nievera, Christian
•
Han, Ming-Hu
•
Shen, Li
•
Zhang, H Steve
more
Date Issued
October 2014
Journal
Nature Neuroscience
Publisher
Nature Publishing Group
Citation
Heller, Elizabeth A, Hannah M Cates, Catherine J Pena, Haosheng Sun, Ningyi Shao, Jian Feng, Sam A Golden, et al. “Locus-Specific Epigenetic Remodeling Controls Addiction- and Depression-Related Behaviors.” Nature Neuroscience 17, no. 12 (October 27, 2014): 1720–27.
Version
Author's final manuscript
Abstract
Chronic exposure to drugs of abuse or stress regulates transcription factors, chromatin-modifying enzymes and histone post-translational modifications in discrete brain regions. Given the promiscuity of the enzymes involved, it has not yet been possible to obtain direct causal evidence to implicate the regulation of transcription and consequent behavioral plasticity by chromatin remodeling that occurs at a single gene. We investigated the mechanism linking chromatin dynamics to neurobiological phenomena by applying engineered transcription factors to selectively modify chromatin at a specific mouse gene in vivo. We found that histone methylation or acetylation at the Fosb locus in nucleus accumbens, a brain reward region, was sufficient to control drug- and stress-evoked transcriptional and behavioral responses via interactions with the endogenous transcriptional machinery. This approach allowed us to relate the epigenetic landscape at a given gene directly to regulation of its expression and to its subsequent effects on reward behavior.
MIT Department
Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
McGovern Institute for Brain Research at MIT
Terms of Use
Creative Commons Attribution-Noncommercial-Share Alike
http://creativecommons.org/licenses/by-nc-sa/4.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/102587
DOI of Published Version
https://doi.org/10.1038/nn.3871
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.