The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
ATR‐dependent phosphorylation and activation of ATM in response to UV treatment or replication fork stalling
Open accessAbstract
The phosphatidyl inositol 3-kinase-like kinases (PIKKs), ataxia-telangiectasia mutated (ATM) and ATM- and Rad3-related (ATR) regulate parallel damage response signalling pathways. ATM is reported to be activated by DNA double-strand breaks (DSBs), whereas ATR is recruited to single-stranded regions of DNA. Although the two pathways were considered to function independently, recent studies have demonstrated that ATM functions upstream of ATR following exposure to ionising radiation (IR) in S/G2. Here, we show that ATM phosphorylation at Ser1981, a characterised autophosphorylation site, is ATR-dependent and ATM-independent following replication fork stalling or UV treatment. In contrast to IR-induced ATM-S1981 phosphorylation, UV-induced ATM-S1981 phosphorylation does not require the Nbs1 C-terminus or Mre11. ATR-dependent phosphorylation of ATM activates ATM phosphorylation of Chk2, which has an overlapping function with Chk1 in regulating G2/M checkpoint arrest. Our findings provide insight into the interplay between the PIKK damage response pathways.
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“In contrast to the IR situation, UV-induced ATM phosphorylation at Serine 1981 does not require the MRN complex, which is a requirement for ATM activation by DSBs.”
From Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress (2014) · cites this paper as [144]
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“ATR-dependent ATM activation promotes Chk2 phosphorylation downstream of the checkpoint signaling [144].”
From Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress (2014) · cites this paper as [144]
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“ATM auto-phosphorylation at Ser1981 is ATR-dependent and ATM-independent in response to stalled DNA replication forks or UV-induced DNA damage [144].”
From Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress (2014) · cites this paper as [144]
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Citations
Cites
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Metadata
- Authors
- Stiff, T., Walker, S. A., Cerosaletti, K., Goodarzi, A. A., Petermann, E., Concannon, P., O'Driscoll, M., & Jeggo, P. A.
- Affiliations
- University of Sussex (GB)
- Benaroya Research Institute (US)
- Corresponding author
- Jeggo, Penny A
- Venue
- The EMBO Journal
- Published
- 2006-11-23
- Volume
- 25
- Issue
- 24
- Pages
- 5775-5782
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC1698893
- OpenAlex
- W2018458310
- Cited by
- 360
- References
- 31
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 7 · 2023: 6 · 2022: 10 · 2021: 12 · 2020: 11 · 2019: 18 · 2018: 11 · 2017: 17 · 2016: 14 · 2015: 20 · 2014: 20 · 2013: 29 · 2012: 27
- FWCI
- 13.20
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- The EMBO Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Figshare (submittedVersion, cc-by)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
- Sussex Research Online (University of Sussex) (submittedVersion)
- Funders
- National Cancer Institute (CA 57569, R01CA057569)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- ATM, ATR, ATM phosphorylation, replication fork stalling, UV-induced DNA damage, Chk2 phosphorylation, NBS1, MRE11, DNA double-strand breaks, single-stranded DNA
- MeSH terms
- Checkpoint Kinase 1, Animals, DNA Replication, DNA-Binding Proteins, Enzyme Activation, Fibroblasts, Histones, Humans, Hydroxyurea, Mitosis, Models, Biological, Nuclear Proteins, Phosphoproteins, Phosphorylation, Phosphoserine, Protein Kinases, Ultraviolet Rays, G2 Phase, Protein Serine-Threonine Kinases, Protein Structure, Tertiary, Cell Cycle Proteins, Tumor Suppressor Proteins, Mice, Ataxia Telangiectasia Mutated Proteins, Checkpoint Kinase 2
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