Yamane K, Katayama E, Sugasawa K, Tsuruo T
Laboratory of Biomedical Research, Institute of Molecular and Cellular Biosciences, The University of Tokyo, Japan.
Oncogene. 2000 Apr 13;19(16):1982-91. doi: 10.1038/sj.onc.1203528.
The BRCT region, the carboxyl-terminus of BRCA1 (the breast cancer susceptibility gene 1 product), is ubiquitous in several proteins that participate in cell cycle checkpoints and DNA repair. We have previously shown that the BRCT regions of TopBP1 (DNA topoisomerase II binding protein 1) and BRCA1 bound DNA breaks. A BRCT-related region, BRCT-W1, in the retinoblastoma susceptibility gene product (Rb) also could bind DNA fragments, independently of DNA sequences. Five BRCT-W regions were found in the Rb family. All BRCT-Ws of Rb bound DNA fragments. Electron microscopy and treatment with an exonuclease showed that BRCT-Ws bound double-strand DNA breaks. Since some BRCTs are exceptional common relating elements in tumor suppression, our findings reveal novel aspects of the tumor suppression mechanism.
BRCT结构域是乳腺癌易感基因1(BRCA1)的羧基末端,存在于多种参与细胞周期检查点和DNA修复的蛋白质中。我们之前已经表明,TopBP1(DNA拓扑异构酶II结合蛋白1)和BRCA1的BRCT结构域可结合DNA断裂处。视网膜母细胞瘤易感基因产物(Rb)中的一个与BRCT相关的区域BRCT-W1也能独立于DNA序列结合DNA片段。在Rb家族中发现了五个BRCT-W区域。Rb的所有BRCT-W区域都能结合DNA片段。电子显微镜和核酸外切酶处理表明,BRCT-W区域可结合双链DNA断裂处。由于一些BRCT是肿瘤抑制中非常常见的相关元件,我们的发现揭示了肿瘤抑制机制的新方面。