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Journal ArticleDOI

ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage

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TLDR
A large-scale proteomic analysis of proteins phosphorylated in response to DNA damage on consensus sites recognized by ATM and ATR is performed and more than 900 regulated phosphorylation sites encompassing over 700 proteins are identified.
Abstract
Cellular responses to DNA damage are mediated by a number of protein kinases, including ATM (ataxia telangiectasia mutated) and ATR (ATM and Rad3-related). The outlines of the signal transduction portion of this pathway are known, but little is known about the physiological scope of the DNA damage response (DDR). We performed a large-scale proteomic analysis of proteins phosphorylated in response to DNA damage on consensus sites recognized by ATM and ATR and identified more than 900 regulated phosphorylation sites encompassing over 700 proteins. Functional analysis of a subset of this data set indicated that this list is highly enriched for proteins involved in the DDR. This set of proteins is highly interconnected, and we identified a large number of protein modules and networks not previously linked to the DDR. This database paints a much broader landscape for the DDR than was previously appreciated and opens new avenues of investigation into the responses to DNA damage in mammals.

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Journal ArticleDOI

DNA damage and innate immunity: links and trade-offs

TL;DR: Current understanding of the mechanism by which cells sense damaged and foreign DNA is reviewed, including the functional role of DNA damage signaling in immune activation and the relevance of these processes to DNA damage-driven chronic inflammation in disease and in aging.
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ATM protein kinase: the linchpin of cellular defenses to stress.

TL;DR: This review has tried to untangle the complex web of ATM signaling pathways with the purpose of pinpointing multiple roles of ATM underlying the complex phenotypes observed in AT patients.
Journal ArticleDOI

The Role of the Mammalian Target of Rapamycin (mTOR) in Pulmonary Fibrosis.

TL;DR: The pathological role of mTOR kinase in pulmonary fibrosis is discussed and how mTOR inhibitors may mitigate fibrotic progression is examined, to suggest an attractive and unique therapeutic target in lung fibrosis.
Journal ArticleDOI

ATM protein kinase mediates full activation of Akt and regulates glucose transporter 4 translocation by insulin in muscle cells.

TL;DR: To investigate the function of ATM in insulin signal transduction, insulin resistance was induced in rats by feeding them a high-fat diet and decreased ATM expression suggests that ATM is involved in the development of insulin resistance through down-regulation of Akt activity.
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An extra allele of Chk1 limits oncogene-induced replicative stress and promotes transformation

TL;DR: Protection from replicative stress conferred by Chk1 promotes transformation and reduces the likelihood of cell death and promotes transformation in response to infectious disease.
References
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Journal ArticleDOI

The DNA damage response: putting checkpoints in perspective

TL;DR: The inability to repair DNA damage properly in mammals leads to various disorders and enhanced rates of tumour development, and this work has shown that direct activation of DNA repair networks is needed to correct this problem.
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Cell-cycle checkpoints and cancer

TL;DR: All life on earth must cope with constant exposure to DNA-damaging agents such as the Sun's radiation, and how cells respond to DNA damage are critical determinants of whether that individual will develop cancer.
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DNA damage-induced activation of p53 by the checkpoint kinase Chk2.

TL;DR: Chk2 directly phosphorylated p53 on serine 20, which is known to interfere with Mdm2 binding, and provides a mechanism for increased stability of p53 by prevention of ubiquitination in response to DNA damage.
Journal ArticleDOI

Immunoaffinity profiling of tyrosine phosphorylation in cancer cells

TL;DR: Applying this approach to several cell systems, including cancer cell lines, shows it can be used to identify activated protein kinases and their phosphorylated substrates without prior knowledge of the signaling networks that are activated, a first step in profiling normal and oncogenic signaling networks.
Journal Article

Global Analysis of Protein Phosphorylation in Yeast

TL;DR: The in vitro substrates recognized by most yeast protein kinases are described, with the use of proteome chip technology, and these results will provide insights into the mechanisms and roles of protein phosphorylation in many eukaryotes.
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