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电离辐射诱导的DNA损伤修复蛋白焦点分析

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

作者信息

van Veelen Lieneke R, Cervelli Tiziana, van de Rakt Mandy W M M, Theil Arjan F, Essers Jeroen, Kanaar Roland

机构信息

Department of Cell Biology and Genetics, Erasmus MC, University Medical Center, P.O. Box 1738, 3000 DR Rotterdam, The Netherlands.

出版信息

Mutat Res. 2005 Jul 1;574(1-2):22-33. doi: 10.1016/j.mrfmmm.2005.01.019. Epub 2005 Mar 31.

Abstract

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.

摘要

通过同源重组修复DNA双链断裂需要大量蛋白质。这些蛋白质包括Rad51和Mre11,已知它们会重新定位到DNA损伤位点形成核灶。电离辐射诱导的灶可以通过免疫染色可视化。已发表的数据显示,特定DNA修复蛋白的灶阳性细胞数量和每个细胞核的灶数量存在很大差异。这里描述的实验表明,DNA损伤诱导后的时间不仅影响灶阳性细胞的数量,还影响单个灶的大小。电离辐射剂量影响灶阳性细胞的数量和每个细胞核的灶数量。此外,电离辐射诱导的灶形成取决于细胞的细胞周期阶段和所研究的目标蛋白质。Rad51和Mre11灶似乎相互排斥,尽管一小部分细胞确实显示出这些蛋白质的共定位,这表明在DNA修复过程中的特定时刻这些蛋白质之间可能存在合作。

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