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Early stress evokes dysregulation of histone modifiers in the medial prefrontal cortex across the life span
Author(s) -
Pusalkar Madhavi,
Suri Deepika,
Kelkar Ashwin,
Bhattacharya Amrita,
Galande Sanjeev,
Vaidya Vidita A.
Publication year - 2016
Publication title -
developmental psychobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 93
eISSN - 1098-2302
pISSN - 0012-1630
DOI - 10.1002/dev.21365
Subject(s) - histone , prefrontal cortex , epigenetics , histone methyltransferase , histone h4 , histone acetyltransferases , acetylation , histone methylation , neuroscience , histone h3 , psychology , biology , gene expression , dna methylation , genetics , gene , cognition
Early stress has been hypothesized to recruit epigenetic mechanisms to mediate persistent molecular, cellular, and behavioral changes. Here, we have examined the consequence of the early life stress of maternal separation (ES) on the gene expression of several histone modifiers that regulate histone acetylation and methylation within the medial prefrontal cortex (mPFC), a key limbic brain region that regulates stress responses and mood‐related behavior. ES animals exhibit gene regulation of both writer (histone acetyltransferases and histone methyltransferases) and eraser (histone deacetylases and histone lysine demethylases) classes of histone modifiers. While specific histone modifiers ( Kat2a , Smyd3 , and Suv420h1 ) and the sirtuin, Sirt4 were downregulated across life within the mPFC of ES animals, namely at postnatal Day 21, 2 months, and 15 months of age, we also observed gene regulation restricted to these specific time points. Despite the decline noted in expression of several histone modifiers within the mPFC following ES, this was not accompanied by any change in global or residue‐specific H3 acetylation and methylation. Our findings indicate that ES results in the regulation of several histone modifiers within the mPFC across life, and suggest that such perturbations may contribute to the altered prefrontal structural and functional plasticity observed following early adversity. © 2015 Wiley Periodicals, Inc. Dev Psychobiol 58: 198–210, 2016.