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Abstracts
Cells with mutated autophosphorylation sites in the ABCDE cluster of DNA-dependent protein kinase catalytic subunit (DNA-PKcs) are defective in the repair of ionising radiation-induced DSB, but show in an in vitro test the same DNA-PK activity as the cells possessing wild type enzyme. Nevertheless, the mutated DNA-PK is able to undergo ATP-dependent autophosphorylation and inactivation. This characteristics correspond well with the phenotypic features of the L5178Y-S (LY-S) cell line that is defective in DSB repair, shows a pronounced G1 phase radiosensitivity, but in which the level of DNA-PK activity present in total cell extracts is similar to that of its radioresistant counterpart L5178Y-R (LY-R) cell line. The purpose of this work was to examine the possible alterations in the sequence encoding the cluster of autophosphorylation sites in the DNA-dependent protein kinase in LY-S cells. Despite the presence of phenotypic features indicating the possibility of such alterations, no differences were found between the sequences coding for the autophosphorylation sites in L5178Y-R and L5178Y-S cells. In conclusion, the repair defect in LY-S cells is not related to the structure of the DNA-PK autophosphorylation sites (ABCDE casette).
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Year
Volume
Issue
Pages
233-236
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Dates
published
2006
received
2005-08-31
revised
2005-10-12
accepted
2005-10-24
(unknown)
2006-01-09
Contributors
author
- Department of Radiobiology and Health Protection, Institute of Nuclear Chemistry and Technology, Warszawa, Poland
author
- Department of Radiobiology and Health Protection, Institute of Nuclear Chemistry and Technology, Warszawa, Poland
author
- Department of Radiobiology and Health Protection, Institute of Nuclear Chemistry and Technology, Warszawa, Poland
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Document Type
Publication order reference
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bwmeta1.element.bwnjournal-article-abpv53p233kz