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ATM and ATR: Sensing DNA damage

机译:ATM和ATR:感知DNA损伤

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摘要

Cellular response to genotoxic stress is a very complex process, and it usually starts with the "sensing" or "detection" of the DNA damage, followed by a series of events that include signal transduction and activation of transcription factors. The activated transcription factors induce expressions of many genes which are involved in cellular functions such as DNA repair, cell cycle arrest, and cell death. There have been extensive studies from multiple disciplines exploring the mechanisms of cellular genotoxic responses, which have resulted in the identification of many cellular components involved in this process, including the mitogen-activated protein kinases (MAPKs) cascade. Although the initial activation of protein kinase cascade is not fully understood, human protein kinases ATM (ataxia-telangiectasia, mutated) and ATR (ATM and Rad3-related) are emerging as potential sensors of DNA damage. Current progresses in ATM/ATR research and related signaling pathways are discussed in this review, in an effort to facilitate a better understanding of genotoxic stress response.
机译:细胞对遗传毒性应激的反应是一个非常复杂的过程,通常始于DNA损伤的“感知”或“检测”,随后是一系列事件,包括信号转导和转录因子激活。活化的转录因子诱导许多基因的表达,这些基因参与细胞功能,例如DNA修复,细胞周期停滞和细胞死亡。来自多个学科的广泛研究探索了细胞遗传毒性反应的机制,从而导致鉴定了参与此过程的许多细胞成分,包括促分裂原活化的蛋白激酶(MAPK)级联反应。尽管尚未完全了解蛋白激酶级联反应的初始激活,但人类蛋白激酶ATM(共济失调毛细血管扩张,突变)和ATR(与ATM和Rad3相关)正在成为DNA损伤的潜在传感器。本文综述了ATM / ATR研究和相关信号通路的最新进展,以促进对遗传毒性应激反应的更好理解。

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