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DNA-Dependent Protein Kinase Catalytic Subunit: The Sensor for DNA Double-Strand Breaks Structurally and Functionally Related to Ataxia Telangiectasia Mutated
- Source :
- Genes, Vol 12, Iss 1143, p 1143 (2021), Genes
- Publication Year :
- 2021
- Publisher :
- MDPI AG, 2021.
-
Abstract
- The DNA-dependent protein kinase (DNA-PK) is composed of a DNA-dependent protein kinase catalytic subunit (DNA-PKcs) and Ku70/Ku80 heterodimer. DNA-PK is thought to act as the “sensor” for DNA double-stranded breaks (DSB), which are considered the most deleterious type of DNA damage. In particular, DNA-PKcs and Ku are shown to be essential for DSB repair through nonhomologous end joining (NHEJ). The phenotypes of animals and human individuals with defective DNA-PKcs or Ku functions indicate their essential roles in these developments, especially in neuronal and immune systems. DNA-PKcs are structurally related to Ataxia–telangiectasia mutated (ATM), which is also implicated in the cellular responses to DSBs. DNA-PKcs and ATM constitute the phosphatidylinositol 3-kinase-like kinases (PIKKs) family with several other molecules. Here, we review the accumulated knowledge on the functions of DNA-PKcs, mainly based on the phenotypes of DNA-PKcs-deficient cells in animals and human individuals, and also discuss its relationship with ATM in the maintenance of genomic stability.
- Subjects :
- Ku80
DNA double-stranded break (DSB)
DNA damage
Protein subunit
DNA-dependent protein kinase (DNA-PK)
Ataxia Telangiectasia Mutated Proteins
DNA-Activated Protein Kinase
Review
QH426-470
DNA damage response
DNA-Dependent Protein Kinase Catalytic Subunit
phosphatidylinositol 3-kinase-like kinase (PIKK)
Catalytic Domain
Ku
Genetics
DNA-dependent protein kinase catalytic subunit (DNA-PKcs)
DNA Breaks, Double-Stranded
Protein kinase A
Genetics (clinical)
Ku70
Kinase
Chemistry
protein kinase
Ataxia–telangiectasia mutated (ATM)
Cell biology
Non-homologous end joining
enzymes and coenzymes (carbohydrates)
biological phenomena, cell phenomena, and immunity
Subjects
Details
- Language :
- English
- ISSN :
- 20734425
- Volume :
- 12
- Issue :
- 1143
- Database :
- OpenAIRE
- Journal :
- Genes
- Accession number :
- edsair.doi.dedup.....23f5dc86ecf86445b4e565e2aa86610b