Denton R R, Koszewski N J, Notides A C
Department of Biophysics, University of Rochester School of Medicine and Dentistry, New York 14642.
J Biol Chem. 1992 Apr 15;267(11):7263-8.
We have shown that the 32P-phosphorylation of the nuclear estrogen receptor from human MCF-7 cells or the calf uterus is estrogen-dependent. Within 2 min of estradiol treatment the phosphorylation of the estrogen receptor from MCF-7 cells doubled, and increased 4-fold within 20-40 min of estradiol treatment. Progesterone was ineffective in stimulating the phosphorylation of the estrogen receptor. Phosphoamino acid analysis indicated that the estrogen-stimulated phosphorylation of the human or calf estrogen receptor occurred only on serine residue(s). Phosphotryptic peptide analysis of the human estrogen receptor by two-dimensional peptide mapping or reverse-phase high pressure liquid chromatography revealed that only a single tryptic peptide (site) was phosphorylated. Treatment of the estrogen receptor with potato acid phosphatase resulted in the dephosphorylation of the 32P-labeled estrogen receptor and a decrease of the receptor's affinity for specific DNA sequences. These data suggest that transcriptional activation by the estrogen receptor involves an estrogen-dependent phosphorylation of the receptor resulting in its increased affinity for specific DNA sequences.
我们已经证明,来自人MCF-7细胞或小牛子宫的核雌激素受体的32P磷酸化是雌激素依赖性的。在雌二醇处理的2分钟内,MCF-7细胞雌激素受体的磷酸化增加了一倍,并在雌二醇处理的20-40分钟内增加了4倍。孕酮在刺激雌激素受体的磷酸化方面无效。磷酸氨基酸分析表明,人或小牛雌激素受体的雌激素刺激的磷酸化仅发生在丝氨酸残基上。通过二维肽图谱或反相高压液相色谱对人雌激素受体进行磷酸化胰蛋白酶肽分析表明,只有一个胰蛋白酶肽(位点)被磷酸化。用马铃薯酸性磷酸酶处理雌激素受体导致32P标记的雌激素受体去磷酸化,并降低受体对特定DNA序列的亲和力。这些数据表明,雌激素受体的转录激活涉及受体的雌激素依赖性磷酸化,从而导致其对特定DNA序列的亲和力增加。