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Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

Postal Subscription Code 80-969

2018 Impact Factor: 2.809

Front Chem Sci Eng    2011, Vol. 5 Issue (2) : 179-187    https://doi.org/10.1007/s11705-009-0268-4
RESEARCH ARTICLE
Functional role of ATM in the cellular response to DNA damage
Ming LIU1, Wenxiang HU2()
1. College of Life Science, Capital Normal University, Beijing 100048, China; 2. Institute of Physical Organic and Medicinal Chemistry, Capital Normal University, Beijing 100048, China
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Abstract

Ataxia-telangiectasia mutated (ATM) plays a key role in regulating the cellular response to ionizing radiation. The tumor-suppressor gene ATM, mutations in which cause the human genetic disease ataxia telangiectasia, encodes a key protein kinase that controls the cellular response to double-stranded breaks. Activation of ATM results in phosphorylation of many downstream targets that modulate numerous damage response pathways, most notably cell cycle checkpoints. Here, we highlight some of the new developments in the field in our understanding of the mechanism of activation of ATM and its signaling pathways, explore whether DNA double-strand breaks are the sole activators of ATM and ATM-dependent signaling pathways, and address some of the prominent, unanswered questions related to ATM and its function. The scope of this article is to provide a brief overview of the recent literature on this subject and to raise questions that could be addressed in future studies.

Keywords ataxia-telangiectasia mutated (ATM)      cell cycle checkpoint      DNA damage      signalling transduction     
Corresponding Author(s): HU Wenxiang,Email:huwx66@163.com   
Issue Date: 05 June 2011
 Cite this article:   
Ming LIU,Wenxiang HU. Functional role of ATM in the cellular response to DNA damage[J]. Front Chem Sci Eng, 2011, 5(2): 179-187.
 URL:  
https://academic.hep.com.cn/fcse/EN/10.1007/s11705-009-0268-4
https://academic.hep.com.cn/fcse/EN/Y2011/V5/I2/179
Fig.1  Schematic hierarchical representation of the factors activated following the generation of DNA damage []
Fig.2  Protein phosphatases in DNA damage checkpoint signaling []
Fig.3  ATM kinases in DNA damage checkpoint signaling [,]
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