表观基因组
染色质
乙酰化
组蛋白
生物
表观遗传学
酶
转录调控
基因表达调控
细胞生物学
生物化学
胞浆
基因
乙酰辅酶A
新陈代谢
基因表达
DNA甲基化
作者
Sharanya Sivanand,Isabella Viney,Kathryn E. Wellen
标识
DOI:10.1016/j.tibs.2017.11.004
摘要
The epigenome is sensitive to the availability of metabolites that serve as substrates of chromatin-modifying enzymes. Links between acetyl-CoA metabolism, histone acetylation, and gene regulation have been documented, although how specificity in gene regulation is achieved by a metabolite has been challenging to answer. Recent studies suggest that acetyl-CoA metabolism is tightly regulated both spatially and temporally to elicit responses to nutrient availability and signaling cues. Here we discuss evidence that acetyl-CoA production is differentially regulated in the nucleus and cytosol of mammalian cells. Recent findings indicate that acetyl-CoA availability for site-specific histone acetylation is influenced through post-translational modification of acetyl-CoA-producing enzymes, as well as through dynamic regulation of the nuclear localization and chromatin recruitment of these enzymes.
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