Ishida Takako, Takizawa Yoshimasa, Kainuma Takashi, Inoue Jin, Mikawa Tsutomu, Shibata Takehiko, Suzuki Hidekazu, Tashiro Satoshi, Kurumizaka Hitoshi
Laboratory of Structural Biology, Graduate School of Advanced Science and Engineering, Waseda University, 2-2 Wakamatsu-cho, Shinjuku-ku, Tokyo 162-8480, Japan.
Nucleic Acids Res. 2009 Jun;37(10):3367-76. doi: 10.1093/nar/gkp200. Epub 2009 Mar 30.
RAD51, an essential eukaryotic DNA recombinase, promotes homologous pairing and strand exchange during homologous recombination and the recombinational repair of double strand breaks. Mutations that up- or down-regulate RAD51 gene expression have been identified in several tumors, suggesting that inappropriate expression of the RAD51 activity may cause tumorigenesis. To identify chemical compounds that affect the RAD51 activity, in the present study, we performed the RAD51-mediated strand exchange assay in the presence of 185 chemical compounds. We found that 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS) efficiently inhibited the RAD51-mediated strand exchange. DIDS also inhibited the RAD51-mediated homologous pairing in the absence of RPA. A surface plasmon resonance analysis revealed that DIDS directly binds to RAD51. A gel mobility shift assay showed that DIDS significantly inhibited the DNA-binding activity of RAD51. Therefore, DIDS may bind near the DNA binding site(s) of RAD51 and compete with DNA for RAD51 binding.
RAD51是一种必需的真核生物DNA重组酶,在同源重组及双链断裂的重组修复过程中促进同源配对和链交换。在多种肿瘤中已鉴定出上调或下调RAD51基因表达的突变,这表明RAD51活性的异常表达可能导致肿瘤发生。为了鉴定影响RAD51活性的化合物,在本研究中,我们在185种化合物存在的情况下进行了RAD51介导的链交换试验。我们发现4,4'-二异硫氰基芪-2,2'-二磺酸(DIDS)能有效抑制RAD51介导的链交换。在没有RPA的情况下,DIDS也抑制RAD51介导的同源配对。表面等离子体共振分析表明DIDS直接与RAD51结合。凝胶迁移率变动分析表明DIDS显著抑制RAD51的DNA结合活性。因此,DIDS可能结合在RAD51的DNA结合位点附近,并与DNA竞争RAD51的结合。