ten Heggler-Bordier B, Claret F X, Wahli W
Institut de Biologie animale, Université de Lausanne, Switzerland.
J Mol Biol. 1988 Nov 5;204(1):217-20. doi: 10.1016/0022-2836(88)90612-2.
Using an extract of nuclei from the estrogen-responsive human breast cancer cell line MCF-7, protein-DNA complexes were assembled in vitro at the 5' end of the Xenopus laevis vitellogenin gene B2 that is normally expressed in liver after estrogen induction. The complexes formed were analyzed by electron microscopy after labeling by the indirect colloidal gold immunological method using a monoclonal antibody specific for the human estrogen receptor. As identified by its interaction with protein A-gold, the antibody was found linked to two protein-DNA complexes, the first localized at the estrogen responsive element of the gene and the second in intron I, thus proving a direct participation of the receptor in these two complexes. The procedure used allows the visualization and rapid localization of specific transcription factors bound in vitro to a promoter or any other gene region.
利用雌激素反应性人乳腺癌细胞系MCF-7的细胞核提取物,在非洲爪蟾卵黄蛋白原基因B2的5'端体外组装蛋白质-DNA复合物,该基因在雌激素诱导后通常在肝脏中表达。使用针对人雌激素受体的单克隆抗体,通过间接胶体金免疫学法标记后,用电镜分析形成的复合物。通过其与蛋白A-金的相互作用鉴定,发现该抗体与两种蛋白质-DNA复合物相连,第一种定位于基因的雌激素反应元件处,第二种在内含子I中,从而证明受体直接参与了这两种复合物的形成。所采用的方法能够可视化并快速定位体外与启动子或任何其他基因区域结合的特定转录因子。