Analysis of ionizing radiation-induced foci of DNA damage repair proteins

被引:56
作者
van Veelen, LR
Cervelli, T
van de Rakt, MWMM
Theil, AF
Essers, J
Kanaar, R
机构
[1] Erasmus Univ, Med Ctr, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dr Daniel Den Hoed Canc Ctr, Dept Radiat Oncol, NL-3008 AE Rotterdam, Netherlands
[3] CNR, Lab Gene & Mol Therapy, Inst Clin Physiol, I-56124 Pisa, Italy
关键词
homologous recombination; non-homologous DNA end joining; cell cycle; Rad51; Mre11;
D O I
10.1016/j.mrfmmm.2005.01.019
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Repair of DNA double-strand breaks by homologous recombination requires an extensive set of proteins. Among these proteins are Rad51 and Mre11, which are known to re-localize to sites of DNA damage into nuclear foci. Ionizing radiation-induced foci can be visualized by immuno-staining. Published data show a large variation in the number of foci-positive cells and number of foci per nucleus for specific DNA repair proteins. The experiments described here demonstrate that the time after induction of DNA damage influenced not only the number of foci-positive cells, but also the size of the individual foci. The dose of ionizing radiation influenced both the number of foci-positive cells and the number of foci per nucleus. Furthermore, ionizing radiation-induced foci formation depended on the cell cycle stage of the cells and the protein of interest that was investigated. Rad51 and Mre11 foci seemed to be mutually exclusive, though a small subset of cells did show co-localization of these proteins, which suggests a possible cooperation between the proteins at a specific moment during DNA repair. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:22 / 33
页数:12
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