Synapsis of DNA ends by DNA-dependent protein kinase

被引:249
作者
DeFazio, LG
Stansel, RM
Griffith, JD
Chu, G [1 ]
机构
[1] Stanford Univ, Dept Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
[3] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
关键词
DNA-dependent protein kinase; DNA repair; electron microscopy; non-homologous end-joining; V(D)J recombination;
D O I
10.1093/emboj/cdf299
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 catalytic subunit of DNA-dependent protein kinase (DNA-PKCS) is required for a non-homologous end-joining pathway that repairs DNA double-strand breaks produced by ionizing radiation or V(D)J recombination; however, its role in this pathway has remained obscure. Using a neutravidin pull-down assay. we found that DNA-PKCS mediates formation of a synaptic complex containing two DNA molecules. Furthermore. kinase activity was cooperative with respect to DNA concentration, suggesting that activation of the kinase occurs only after DNA synapsis. Electron microscopy revealed complexes of two DNA ends brought together by two DNA-PKCS molecules. Our results suggest that DNA-PKCS brings DNA ends together and then undergoes activation of its kinase, presumably to regulate subsequent steps for processing and ligation of the ends.
引用
收藏
页码:3192 / 3200
页数:9
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