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HIF1-regulated ATRIP expression is required for hypoxia induced ATR activation
- Source :
- FEBS Letters. (7):930-935
- Publisher :
- Published by Elsevier B.V.
-
Abstract
- The ATR–ATRIP protein kinase complex plays a crucial role in the cellular response to replication stress and DNA damage. Recent studies found that ATR could be activated in response to hypoxia and be involved in hypoxia-induced genetic instability in cancer cells. However, the underlying mechanisms for ATR activation in response to hypoxic stress are still not fully understood. We reported that ATRIP is a direct target of HIF-1. Silencing the expression of HIF-1α in cancer cells by RNA interference abolished hypoxia-induced ATRIP expression. Silencing the expression of ATRIP by RNA interference abolished hypoxia induced ATR activation and CHK1 phosphorylation in cancer cells. Taken together, these data shed novel insights on the mechanism of hypoxia-induced activation of the ATR pathway.
- Subjects :
- Protein kinase complex
Chromatin Immunoprecipitation
DNA damage
Blotting, Western
Biophysics
Cell Cycle Proteins
Ataxia Telangiectasia Mutated Proteins
Biology
Protein Serine-Threonine Kinases
Response Elements
Biochemistry
Cell Line
Structural Biology
RNA interference
ATRIP
Neoplasms
Genetics
medicine
Gene silencing
Humans
Phosphorylation
Promoter Regions, Genetic
Hypoxia
Molecular Biology
Adaptor Proteins, Signal Transducing
Binding Sites
Reverse Transcriptase Polymerase Chain Reaction
HIF-1
Cell Biology
Hep G2 Cells
Hypoxia (medical)
Hypoxia-Inducible Factor 1, alpha Subunit
Cell Hypoxia
Cell biology
DNA-Binding Proteins
Gene Expression Regulation, Neoplastic
HEK293 Cells
ATR
Cancer cell
Checkpoint Kinase 1
MCF-7 Cells
RNA Interference
medicine.symptom
biological phenomena, cell phenomena, and immunity
Protein Kinases
Hypoxic stress
HeLa Cells
Protein Binding
Subjects
Details
- Language :
- English
- ISSN :
- 00145793
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....4b1e0cc1038022721767bb0e548892c8
- Full Text :
- https://doi.org/10.1016/j.febslet.2013.02.020