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Three Decades of Research on O-GlcNAcylation – A Major Nutrient Sensor That Regulates Signaling Transcription and Cellular Metabolism

机译:O-GlcNAcylation研究的三个十年-一种主要的营养传感器可调节信号传导转录和细胞代谢

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摘要

Even though the dynamic modification of polypeptides by the monosaccharide, O-linked N-acetylglucosamine (O-GlcNAcylation) was discovered over 30 years ago, its physiological significance as a major nutrient sensor that regulates myriad cellular processes has only recently been more widely appreciated. O-GlcNAcylation, either on its own or by its interplay with other post-translational modifications, such as phosphorylation, ubiquitination, and others, modulates the activities of signaling proteins, regulates most components of the transcription machinery, affects cell cycle progression and regulates the targeting/turnover or functions of myriad other regulatory proteins, in response to nutrients. Acute increases in O-GlcNAcylation protect cells from stress-induced injury, while chronic deregulation of O-GlcNAc cycling contributes to the etiology of major human diseases of aging, such as diabetes, cancer, and neurodegeneration. Recent advances in tools to study O-GlcNAcylation at the individual site level and specific inhibitors of O-GlcNAc cycling have allowed more rapid progress toward elucidating the specific functions of O-GlcNAcylation in essential cellular processes.
机译:尽管三十多年前就发现了单糖对多肽的动态修饰,O-连接的N-乙酰氨基葡糖(O-GlcNAcylation),但作为调节多种细胞过程的主要营养传感器的生理意义直到最近才被广泛认识。 O-GlcNAcylation本身或与其他翻译后修饰(如磷酸化,泛素化等)的相互作用,可调节信号蛋白的活性,调节转录机制的大多数成分,影响细胞周期进程并调节响应营养素而靶向/转换或调节其他多种调节蛋白的功能。 O-GlcNAc酰化的急剧增加可保护细胞免受应激诱导的损伤,而O-GlcNAc循环的长期失调则助长了人类主要衰老的病因,例如糖尿病,癌症和神经退行性变。在单个位点水平上研究O-GlcNAcy的工具和O-GlcNAc循环的特定抑制剂的最新进展,使得在阐明基本细胞过程中O-GlcNAcy的特定功能方面取得了更快的进展。

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