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作 者:周岩[1,2] 丁丽华[1] 程龙[1] 游松[3] 叶棋浓[1]
机构地区:[1]军事医学科学院生物工程研究所 [2]沈阳药科大学,辽宁沈阳110016 [3]沈阳药科大学
出 处:《生物技术通讯》2008年第5期670-672,共3页Letters in Biotechnology
基 金:国家自然科学基金(30500091);全军"十一五"医学科研基金(06J021)
摘 要:目的:构建雌激素受体(ER)β潜在磷酸化位点突变体,并在人胚肾细胞293T中检测其对ERβ下游基因转录的影响。方法:通过ERα和ERβ序列同源性比对,寻找ERβ的潜在磷酸化位点;以pcDNA3-ERβ-FLAG为模板,通过重组PCR,将ERβ264位、469位Ser编码基因突变为Ala编码基因,将突变片段连接到同样双酶切的pcDNA3-FLAG载体中,Western blot检测其表达;将重组质粒转入293T细胞中,检测突变体对含雌激素应答元件(ERE)的报告基因转录活性的影响。结果:ERα和ERβ序列同源性比对发现ERβ的264位Ser和469位Ser可能是其潜在的磷酸化位点;构建了ERβ264位和469位2个点突变体载体pcDNA3-FLAG-ERβ(S264A)和pcDNA3-FLAG-ERβ(S469A),Western blot可检测到ERβ突变体融合蛋白在293T细胞中表达。萤光素酶活性检测表明,在没有雌激素刺激的情况下,2个突变体的活性较野生型没有变化;加入雌激素后,突变体的活性较野生型略有升高。结论:ERβ的264位和469位Ser位点的磷酸化可能不是ERβ调节下游基因转录所必需的,活性升高可能是由于ERβ构象变化造成的。Objective: To construct the potent phosphorylation sites mutants of estrogen reeeptor(ER)β and to detect the effect of the mutants on ERβ transcriptional activity in 293T cell. Methods: Fingding the potent phosphorylation sites mutants of ERβ through comparing homologous sequences of ERα and ERβ. Using recombinant PCR, the coden of Ser^264 and Ser^469 of ERβ were mutated to one of Ala, and the mutated fragments were inserted into the vector pcDNA3-FLAG. The recombinants were transfected into 293T cells, to determine the effects of the mutants on ERβ transcriptional activity. Results: The Ser^264 and Ser^469 of ERβ might be phosphorylation sites of ERβ. The recombinant plasmids, pcDNA3-FLAG-ERβ (S264A) and pcDNA3-FLAG-ERβ (S469A), were constructed. Western blot assay showed that the mutants were expressed in 293T cell. Compared with wild type, the mutants had no effect on the ERE-LUC reporter when estrogen E2 was absent. When E2 was present, the transcriptional activity of mutants was slightly higher than that of the wild type. Conclusion: Ser^264 and Ser^469 might not be the necessary phosphorylation sites and the higher activity of mutants might be due to the changed conformation of ERβ.
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