Jost J P, Seldran M, Geiser M
Proc Natl Acad Sci U S A. 1984 Jan;81(2):429-33. doi: 10.1073/pnas.81.2.429.
DNA-cellulose competition binding assays were used to measure the ability of cloned DNA fragments of the chicken vitellogenin II gene to displace the estrogen-receptor complex from total chicken DNA coupled to cellulose. The DNA fragment that gave the highest competition is situated in the upstream region of the gene between nucleotides -458 and -725. This DNA fragment has four small clusters of A + T-rich sequences and contains the estrogen-dependent hypomethylation site. In vitro methylation of the Msp I site does not change the capacity of the DNA fragment to compete for estrogen-receptor complex, whereas cleavage of the C-C-G-G (Msp I site) results in a complete loss of competition of this fragment for estrogen-receptor complex. These results, combined with deoxyribonuclease I protection experiments, suggest that the most probable binding site for estrogen-receptor complex is . . .G-C-G-T-G-A-C-C-G-G-A-G-C-T-G-A-A-A-G-A-A-C-A-C. . . . This sequence has 73% homology with the core enhancer sequence of simian virus 40, . . .G-G-T-G-T-G-G-A-A-A-G. . . (identical bases italicized).
采用DNA-纤维素竞争结合试验来测定鸡卵黄生成素II基因的克隆DNA片段从与纤维素偶联的总鸡DNA中置换雌激素受体复合物的能力。竞争能力最强的DNA片段位于该基因上游区域核苷酸-458至-725之间。此DNA片段有四个富含A+T的小序列簇,并含有雌激素依赖性低甲基化位点。Msp I位点的体外甲基化不会改变该DNA片段竞争雌激素受体复合物的能力,而切割C-C-G-G(Msp I位点)会导致该片段完全丧失竞争雌激素受体复合物的能力。这些结果与脱氧核糖核酸酶I保护实验相结合,表明雌激素受体复合物最可能的结合位点是……G-C-G-T-G-A-C-C-G-G-A-G-C-T-G-A-A-A-G-A-A-C-A-C……。该序列与猿猴病毒40的核心增强子序列……G-G-T-G-T-G-G-A-A-A-G……有73%的同源性(相同碱基用斜体表示)。