Histone variant H2BE enhances chromatin accessibility in neurons to promote synaptic gene expression and long-term memory
Emily R. FeiermaniD, Sean Louzon, Nicholas A. PrescottiD, Tracy Biaco, Qingzeng GaoiD, Qi QiuiD, Kyuhyun ChoiiD, Katherine C. PalozolaiD, Anna J. VossiD, Shreya D. Mehta, Camille N. Quaye, Katherine T. Lynch, Marc Vincent FuccilloiD, Hao WuiD, Yael DavidiD, Erica KorbiD
Abstract
Regulation of histone proteins affects gene expression through multiple mechanisms including exchange with histone variants. However, widely expressed variants of H2B remain elusive. Recent findings link histone variants to neurological disorders, yet few are well studied in the brain. We applied new tools including novel antibodies, biochemical assays, and sequencing approaches to reveal broad expression of the H2B variant H2BE, and defined its role in regulating chromatin structure, neuronal transcription, and mouse behavior. We find that H2BE is enriched at promoters and a single unique amino acid allows it to dramatically enhance chromatin accessibility. Lastly, we show that H2BE is critical for synaptic gene expression and long-term memory. Together, these data reveal a novel mechanism linking histone variants to chromatin regulation, neuronal function, and memory. This work further identifies the first widely expressed H2B variant and uncovers a single histone amino acid with profound effects on genomic structure.
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