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Updated: Jan 24, 2026

Purification of H3 and H4 Histone Proteins and the Quantification of Acetylated Histone Marks in Cells and Brain Tissue
Published on: November 30, 2018
Isolation and Quantification Brain Region-Specific and Cell Subtype-Specific Histone (De)Acetylation in Cognitive
1Laboratory of Behavioral Neuroscience, Neurocognitive Aging Section, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA. craig.myrum@nih.gov.
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The acetylation of histone tails, which relaxes compact chromatin structure and enhances the accessibility of DNA to regulatory proteins, has emerged as a key mechanism for regulating gene expression. These modifications in turn play critical roles in forming long-term memories. Chromatin immunoprecipitation (ChIP) experiments have enabled the identification of specific histone modifications and the genes most closely associated with active memory formation. Problematically, however, the majority of these studies analyze diverse populations of cell homogenates obtained from the gross dissection of large brain regions. The protocol outlined here uses methods to ascribe gene-specific histone modifications (via specific antibodies and RT-qPCR) to specific cell subtypes (via specific antibodies and cell sorting) in discrete memory-related brain regions (via microdissection) to more precisely identify the role of histone acetylation and deacetylation in cognitive neuroepigenetics.
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