Literature DB >> 28890149

Distinct roles for the deacetylase domain of HDAC3 in the hippocampus and medial prefrontal cortex in the formation and extinction of memory.

Yasaman Alaghband1, Janine L Kwapis2, Alberto J López1, André O White1, Osasumwen V Aimiuwu1, Amni Al-Kachak1, Kasuni K Bodinayake1, Nicole C Oparaugo1, Richard Dang2, Mariam Astarabadi1, Dina P Matheos3, Marcelo A Wood4.   

Abstract

Histone deacetylases (HDACs) are chromatin modifying enzymes that have been implicated as powerful negative regulators of memory processes. HDAC3has been shown to play a pivotal role in long-term memory for object location as well as the extinction of cocaine-associated memory, but it is unclear whether this function depends on the deacetylase domain of HDAC3. Here, we tested whether the deacetylase domain of HDAC3has a role in object location memory formation as well as the formation and extinction of cocaine-associated memories. Using a deacetylase-dead point mutant of HDAC3, we found that selectively blocking HDAC3 deacetylase activity in the dorsal hippocampus enhanced long-term memory for object location, but had no effect on the formation of cocaine-associated memory. When this same point mutant virus of HDAC3 was infused into the prelimbic cortex, it failed to affect cocaine-associated memory formation. With regards to extinction, impairing the HDAC3 deacetylase domain in the infralimbic cortex had no effect on extinction, but a facilitated extinction effect was observed when the point mutant virus was delivered to the dorsal hippocampus. These results suggest that the deacetylase domain of HDAC3 plays a selective role in specific brain regions underlying long-term memory formation of object location as well as cocaine-associated memory formation and extinction.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Chromatin; Conditioned place preference; Dorsal hippocampus; Epigenetics; Long-term memory; Object location

Mesh:

Substances:

Year:  2017        PMID: 28890149      PMCID: PMC5698127          DOI: 10.1016/j.nlm.2017.09.001

Source DB:  PubMed          Journal:  Neurobiol Learn Mem        ISSN: 1074-7427            Impact factor:   2.877


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