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Mol. Cells 2002; 13(2): 159-166

Published online January 1, 1970

© The Korean Society for Molecular and Cellular Biology

DNA-dependent Protein Kinase Complex: a Multifunctional Protein in DNA Repair and Damage Checkpoint

Suk-Hee Lee, Chung-Hui Kim

Abstract

DNA-dependent protein kinase (DNA-PK) is a nuclear serine/threonine protein kinase that is activated upon DNA damage generated by ionizing radiation or UV-irradiation. It is a three-protein complex consisting of a 470-kDa catalytic subunit (DNA-PKcs) and the regu-latory DNA binding subunits, Ku heterodimer (Ku70 and Ku80). Mouse and human cells deficient in DNA-PKcs are hypersensitive to ionizing radiation and de-fective in V(D)J recombination, suggesting a role for the kinase in double-strand break repair and recombi-nation. The Ku heterodimer binds to double-strand DNA breaks produced by either DNA damage or re-combination, protects DNA ends from degradation, orients DNA ends for re-ligation, and recruits its cata-lytic subunit and additional factors necessary for suc-cessful end-joining. DNA-PK is also involved in an early stage of damage-induced cell cycle arrest, how-ever, it remains unclear how the enzyme senses DNA damage and transmits signals to downstream gene(s) and proteins.

Keywords DNA Damage, DSB Repair, DNA-PK, Damage Checkpoint

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Minireview

Mol. Cells 2002; 13(2): 159-166

Published online April 30, 2002

Copyright © The Korean Society for Molecular and Cellular Biology.

DNA-dependent Protein Kinase Complex: a Multifunctional Protein in DNA Repair and Damage Checkpoint

Suk-Hee Lee, Chung-Hui Kim

Abstract

DNA-dependent protein kinase (DNA-PK) is a nuclear serine/threonine protein kinase that is activated upon DNA damage generated by ionizing radiation or UV-irradiation. It is a three-protein complex consisting of a 470-kDa catalytic subunit (DNA-PKcs) and the regu-latory DNA binding subunits, Ku heterodimer (Ku70 and Ku80). Mouse and human cells deficient in DNA-PKcs are hypersensitive to ionizing radiation and de-fective in V(D)J recombination, suggesting a role for the kinase in double-strand break repair and recombi-nation. The Ku heterodimer binds to double-strand DNA breaks produced by either DNA damage or re-combination, protects DNA ends from degradation, orients DNA ends for re-ligation, and recruits its cata-lytic subunit and additional factors necessary for suc-cessful end-joining. DNA-PK is also involved in an early stage of damage-induced cell cycle arrest, how-ever, it remains unclear how the enzyme senses DNA damage and transmits signals to downstream gene(s) and proteins.

Keywords: DNA Damage, DSB Repair, DNA-PK, Damage Checkpoint

Mol. Cells
Sep 30, 2023 Vol.46 No.9, pp. 527~572
COVER PICTURE
Chronic obstructive pulmonary disease (COPD) is marked by airspace enlargement (emphysema) and small airway fibrosis, leading to airflow obstruction and eventual respiratory failure. Shown is a microphotograph of hematoxylin and eosin (H&E)-stained histological sections of the enlarged alveoli as an indicator of emphysema. Piao et al. (pp. 558-572) demonstrate that recombinant human hyaluronan and proteoglycan link protein 1 (rhHAPLN1) significantly reduces the extended airspaces of the emphysematous alveoli by increasing the levels of TGF-β receptor I and SIRT1/6, as a previously unrecognized mechanism in human alveolar epithelial cells, and consequently mitigates COPD.

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