Yokoyama Hiroshi, Kurumizaka Hitoshi, Ikawa Shukuko, Yokoyama Shigeyuki, Shibata Takehiko
RIKEN Genomic Sciences Center, 1-7-22 Suehiro-cho, Tsurumi, Yokohama 230-0045, Japan.
J Biol Chem. 2003 Jan 24;278(4):2767-72. doi: 10.1074/jbc.M210899200. Epub 2002 Nov 18.
The human Rad51B protein is involved in the recombinational repair of damaged DNA. Chromosomal rearrangements of the Rad51B gene have been found in uterine leiomyoma patients, suggesting that the Rad51B gene suppresses tumorigenesis. In the present study, we found that the purified Rad51B protein bound to single-stranded DNA and double-stranded DNA in the presence of ATP and either Mg(2+) or Mn(2+) and hydrolyzed ATP in a DNA-dependent manner. When the synthetic Holliday junction was present along with the half-cruciform and double-stranded oligonucleotides, the Rad51B protein only bound to the synthetic Holliday junction, which mimics a key intermediate in homologous recombination. In contrast, the human Rad51 protein bound to all three DNA substrates with no obvious preference. Therefore, the Rad51B protein may have a specific function in Holliday junction processing in the homologous recombinational repair pathway in humans.
人类Rad51B蛋白参与受损DNA的重组修复。在子宫平滑肌瘤患者中发现了Rad51B基因的染色体重排,这表明Rad51B基因可抑制肿瘤发生。在本研究中,我们发现纯化的Rad51B蛋白在ATP以及Mg(2+)或Mn(2+)存在的情况下与单链DNA和双链DNA结合,并以DNA依赖的方式水解ATP。当合成霍利迪连接体与半十字形和双链寡核苷酸同时存在时,Rad51B蛋白仅与合成霍利迪连接体结合,该连接体模拟同源重组中的关键中间体。相比之下,人类Rad51蛋白对所有三种DNA底物都有结合,且无明显偏好。因此,Rad51B蛋白可能在人类同源重组修复途径的霍利迪连接体处理中具有特定功能。