Acetyl-CoA synthetase regulates histone acetylation and hippocampal memory

被引:0
|
作者
Philipp Mews
Greg Donahue
Adam M. Drake
Vincent Luczak
Ted Abel
Shelley L. Berger
机构
[1] Epigenetics Institute,Departments of Cell and Developmental Biology
[2] Biology,Iowa Neuroscience Institute
[3] Genetics,undefined
[4] University of Pennsylvania Perelman School of Medicine,undefined
[5] University of Iowa Carver College of Medicine,undefined
来源
Nature | 2017年 / 546卷
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摘要
Metabolic production of acetyl coenzyme A (acetyl-CoA) is linked to histone acetylation and gene regulation, but the precise mechanisms of this process are largely unknown. Here we show that the metabolic enzyme acetyl-CoA synthetase 2 (ACSS2) directly regulates histone acetylation in neurons and spatial memory in mammals. In a neuronal cell culture model, ACSS2 increases in the nuclei of differentiating neurons and localizes to upregulated neuronal genes near sites of elevated histone acetylation. A decrease in ACSS2 lowers nuclear acetyl-CoA levels, histone acetylation, and responsive expression of the cohort of neuronal genes. In adult mice, attenuation of hippocampal ACSS2 expression impairs long-term spatial memory, a cognitive process that relies on histone acetylation. A decrease in ACSS2 in the hippocampus also leads to defective upregulation of memory-related neuronal genes that are pre-bound by ACSS2. These results reveal a connection between cellular metabolism, gene regulation, and neural plasticity and establish a link between acetyl-CoA generation ‘on-site’ at chromatin for histone acetylation and the transcription of key neuronal genes.
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页码:381 / 386
页数:5
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