Ionizing radiation triggers chromatin-bound kin17 complex formation in human cells

被引:30
作者
Biard, DSF
Miccoli, L
Despras, E
Frobert, Y
Créminon, C
Angulo, JF
机构
[1] CEA, DSV, DRR, Lab Genet Radiosensibil, F-92265 Fontenay Aux Roses, France
[2] Ctr Etud Saclay, Direct Sci Vivant, Dept Rech Med,Serv Pharmacol & Immunol, CEA, F-91191 Gif Sur Yvette, France
关键词
D O I
10.1074/jbc.M200321200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human DNA-binding (HSA)kin17 protein cross-reacts with antibodies raised against the stress-activated Escherichia coli RecA protein. We show here that HSAkin17 protein is directly associated with chromosomal DNA as judged by cross-linking experiments on living cells. We detected increased amounts of DNA-bound HSAkin17 protein 24 h after gamma irradiation, with 2.6-fold more (HSA)kin17 molecules after 6 Gy of irradiation (46,000-117,000 molecules). At this time we observed that highly proliferating RKO cells displayed the concentration and co-localization of (HSA)kin17 and replication protein A in nucleoplasmic foci. Our results suggest that 24 h post-irradiation HSAkin17 protein may localize at the sites of unrepaired DNA damages. RKO clones expressing an (HSA)KIN17 antisense transcript (RASK.5 and RASK.13 cells) revealed that reduced (HSA)kin17 protein levels are correlated with a decrease in clonogenic cell growth and cell proliferation, as well as an accumulation of cells in early and mid-S phase. Taken together our observations support the idea that HSAkin17 protein is a DNA maintenance protein involved in the cellular response to the presence of DNA damage and suggest that it helps to overcome the perturbation of DNA replication produced by unrepaired lesions.
引用
收藏
页码:19156 / 19165
页数:10
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