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雌激素受体α启动子与小鼠大脑皮质核蛋白的结合:年龄、性别和性腺类固醇的影响

Binding of estrogen receptor alpha promoter to nuclear proteins of mouse cerebral cortex: effect of age, sex, and gonadal steroids.

作者信息

Thakur M K, Sharma P K

机构信息

Biochemistry and Molecular Biology Laboratory, Department of Zoology, Banaras Hindu University, Varanasi, 221005, India.

出版信息

Biogerontology. 2008 Dec;9(6):467-78. doi: 10.1007/s10522-008-9166-2. Epub 2008 Aug 21.

Abstract

Majority of estrogen actions in the brain are mediated by estrogen receptor (ER) alpha which in turn is regulated by several factors like circulating levels of gonadal steroid hormones 17beta-estradiol and testosterone, sex and age of the organism. The expression of ERalpha is regulated through interaction between cis-elements of its promoter and proteins present in the nuclei. Here, we have used electrophoretic mobility shift assay (EMSA) to analyze the effect of age, sex, 17beta-estradiol, and testosterone on the binding of ERalpha promoter (-91 to +46 bp) to nuclear proteins from the mouse cerebral cortex. EMSA revealed the formation of three specific complexes in all groups. However, the intensity of these complexes varied as a function of age, sex and treatment with 17beta-estradiol and testosterone. Nuclear proteins from the cerebral cortex of both sexes showed reduced binding with promoter fragment in old mice. Further, competition analysis indicated stronger binding in females than males of both ages. The extent of binding was reduced by 17beta-estradiol and testosterone treatment in both ages and sexes. Thus, these findings demonstrate differential binding of nuclear proteins to mouse ERalpha promoter which may account for different functions of estrogen in the brain.

摘要

雌激素在大脑中的大多数作用是由雌激素受体(ER)α介导的,而ERα又受到多种因素的调节,如性腺甾体激素17β-雌二醇和睾酮的循环水平、生物体的性别和年龄。ERα的表达通过其启动子的顺式元件与细胞核中存在的蛋白质之间的相互作用来调节。在这里,我们使用电泳迁移率变动分析(EMSA)来分析年龄、性别、17β-雌二醇和睾酮对ERα启动子(-91至+46 bp)与小鼠大脑皮质核蛋白结合的影响。EMSA显示所有组中均形成了三种特异性复合物。然而,这些复合物的强度随年龄、性别以及17β-雌二醇和睾酮处理而变化。老年小鼠两性大脑皮质的核蛋白与启动子片段的结合减少。此外,竞争分析表明,两个年龄段的雌性比雄性具有更强的结合。两个年龄段和两性中,17β-雌二醇和睾酮处理均降低了结合程度。因此,这些发现表明核蛋白与小鼠ERα启动子的结合存在差异,这可能解释了雌激素在大脑中的不同功能。

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