染色质
生物
表观遗传学
染色质重塑
基因组不稳定性
细胞生物学
DNA修复
琥珀酰化
DNA损伤
遗传学
乙酰化
计算生物学
DNA
基因
作者
Feng Chen,Xin‐Jian He,Wenchao Xu,Li Zhou,Qi Liu,Wei‐Cheng Chen,Wei‐Guo Zhu,Jun Zhang
摘要
The fundamental role of cells in safeguarding the genome's integrity against DNA double-strand breaks (DSBs) is crucial for maintaining chromatin homeostasis and the overall genomic stability. Aberrant responses to DNA damage, known as DNA damage responses (DDRs), can result in genomic instability and contribute significantly to tumorigenesis. Unraveling the intricate mechanisms underlying DDRs following severe damage holds the key to identify therapeutic targets for cancer. Chromatin lysine acylation, encompassing diverse modifications such as acetylation, lactylation, crotonylation, succinylation, malonylation, glutarylation, propionylation, and butyrylation, has been extensively studied in the context of DDRs and chromatin homeostasis. Here, we delve into the modifying enzymes and the pivotal roles of lysine acylation and their crosstalk in maintaining chromatin homeostasis and genome integrity in response to DDRs. Moreover, we offer a comprehensive perspective and overview of the latest insights, driven primarily by chromatin acylation modification and associated regulators.
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