Fan Wenhong, Jin Shunqian, Tong Tong, Zhao Hongcheng, Fan Feiyue, Antinore Michael J, Rajasekaran Baskaran, Wu Min, Zhan Qimin
Department of Radiation Oncology, Cancer Institute, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.
J Biol Chem. 2002 Mar 8;277(10):8061-7. doi: 10.1074/jbc.M110225200. Epub 2002 Jan 3.
BRCA1, a breast and ovarian cancer susceptibility gene, has been implicated in gene regulation. Previous studies demonstrate that BRCA1 induces GADD45, a p53-regulated and stress-inducible gene that plays an important role in cellular response to DNA damage. However, the mechanism(s) by which BRCA1 regulates GADD45 remains unclear. In this report, we have shown that BRCA1 activation of the GADD45 promoter is mediated through the OCT-1 and CAAT motifs located at the GADD45 promoter region. Site-directed mutations of both OCT-1 and CAAT motifs abrogate induction of the GADD45 promoter by BRCA1. Both OCT-1 and CAAT motifs are able to confer BRCA1 inducibility in a non-related minimal promoter. Physical associations of BRCA1 protein with transcription factors Oct-1 and NF-YA, which directly bind to the OCT-1 and CAAT motifs, are established by biotin-streptavidin pull-down and coimmunoprecipitation assays. Such protein interactions are required for interaction of BRCA1 with the GADD45 promoter because either immunodepletion of Oct-1 and NF-YA proteins or mutations in the OCT-1 and CAAT motifs disrupt BRCA1 binding to the GADD45 promoter. These findings indicate that BRCA1 can up-regulate its targeted genes through protein-protein interactions and provide a novel mechanism by which BRCA1 participates in transcriptional regulation.
BRCA1是一种乳腺癌和卵巢癌易感基因,与基因调控有关。先前的研究表明,BRCA1可诱导GADD45,这是一种p53调控且受应激诱导的基因,在细胞对DNA损伤的反应中起重要作用。然而,BRCA1调控GADD45的机制仍不清楚。在本报告中,我们表明BRCA1对GADD45启动子的激活是通过位于GADD45启动子区域的OCT-1和CAAT基序介导的。OCT-1和CAAT基序的定点突变消除了BRCA1对GADD45启动子的诱导。OCT-1和CAAT基序都能够在不相关的最小启动子中赋予BRCA1诱导性。通过生物素-链霉亲和素下拉和免疫共沉淀实验证实了BRCA1蛋白与直接结合OCT-1和CAAT基序的转录因子Oct-1和NF-YA之间的物理相互作用。BRCA1与GADD45启动子的相互作用需要这种蛋白质相互作用,因为Oct-1和NF-YA蛋白的免疫去除或OCT-1和CAAT基序中的突变会破坏BRCA1与GADD45启动子的结合。这些发现表明,BRCA1可以通过蛋白质-蛋白质相互作用上调其靶基因,并提供了一种BRCA1参与转录调控的新机制。