Gildemeister Otto S, Sage Jay M, Knight Kendall L
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
J Biol Chem. 2009 Nov 13;284(46):31945-52. doi: 10.1074/jbc.M109.024646. Epub 2009 Sep 26.
Exposure of cells to DNA-damaging agents results in a rapid increase in the formation of subnuclear complexes containing Rad51. To date, it has not been determined to what extent DNA damage-induced cytoplasmic to nuclear transport of Rad51 may contribute to this process. We have analyzed subcellular fractions of HeLa and HCT116 cells and found a significant increase in nuclear Rad51 levels following exposure to a modest dose of ionizing radiation (2 grays). We also observed a DNA damage-induced increase in nuclear Rad51 in the Brca2-defective cell line Capan-1. To address a possible Brca2-independent mechanism for Rad51 nuclear transport, we analyzed subcellular fractions for two other Rad51-interacting proteins, Rad51C and Xrcc3. Rad51C has a functional nuclear localization signal, and although we found that the subcellular distribution of Xrcc3 was not significantly affected by DNA damage, there was a damage-induced increase in nuclear Rad51C. Furthermore, RNA interference-mediated depletion of Rad51C in HeLa and Capan-1 cells resulted in lower steady-state levels of nuclear Rad51 as well as a diminished DNA damage-induced increase. Our results provide important insight into the cellular regulation of Rad51 nuclear entry and a role for Rad51C in this process.
将细胞暴露于DNA损伤剂会导致含Rad51的亚核复合物形成迅速增加。迄今为止,尚未确定DNA损伤诱导的Rad51从细胞质向细胞核的转运在多大程度上可能促成这一过程。我们分析了HeLa和HCT116细胞的亚细胞组分,发现暴露于适度剂量的电离辐射(2格雷)后,细胞核中Rad51水平显著增加。我们还观察到在Brca2缺陷细胞系Capan-1中,DNA损伤诱导细胞核中Rad51增加。为了探究Rad51核转运可能存在的不依赖Brca2的机制,我们分析了另外两种与Rad51相互作用的蛋白Rad51C和Xrcc3的亚细胞组分。Rad51C具有功能性核定位信号,虽然我们发现Xrcc3的亚细胞分布不受DNA损伤的显著影响,但DNA损伤诱导细胞核中Rad51C增加。此外,RNA干扰介导的HeLa和Capan-1细胞中Rad51C的缺失导致细胞核中Rad51的稳态水平降低,以及DNA损伤诱导的增加减少。我们的结果为Rad51核进入的细胞调控以及Rad51C在此过程中的作用提供了重要见解。