Suppr超能文献

糖皮质激素和孕酮的受体识别DNA调控元件的不同特征。

Receptors for glucocorticosteroid and progesterone recognize distinct features of a DNA regulatory element.

作者信息

von der Ahe D, Renoir J M, Buchou T, Baulieu E E, Beato M

出版信息

Proc Natl Acad Sci U S A. 1986 May;83(9):2817-21. doi: 10.1073/pnas.83.9.2817.

Abstract

The chicken lysozyme gene can be induced in oviduct cells by four classes of steroid hormones, including glucocorticosteroids and progestins. The glucocorticosteroid receptor of rat liver and the progesterone receptor of rabbit uterus both bind, although with different relative affinities, to two sites in the promoter region of the chicken lysozyme gene located, respectively, between 50 and 80 and between 160 and 200 base pairs upstream of the transcription start point. Now we show that the purified progesterone binding unit of the chicken oviduct progesterone receptor (Mr 110,000, or so-called B subunit) generates a DNase I protection pattern ("footprint") in the promoter-distal site that is longer than the footprint generated by the glucocorticosteroid receptor. Methylation protection studies within the promoter-distal binding site identify four contact points for the chicken progesterone receptor and three contact points for the glucocorticosteroid receptor, of which only one is shared by both receptors. Computer graphics models allow one to envisage a different interaction of each receptor with the B form of the DNA double helix.

摘要

鸡溶菌酶基因可被四类甾体激素诱导表达,包括糖皮质激素和孕激素,在输卵管细胞中表达。大鼠肝脏的糖皮质激素受体和兔子宫的孕激素受体均可结合鸡溶菌酶基因启动子区域的两个位点,尽管相对亲和力有所不同,这两个位点分别位于转录起始点上游50至80个碱基对以及160至200个碱基对之间。现在我们发现,纯化后的鸡输卵管孕激素受体的孕激素结合单位(分子量约为110,000,即所谓的B亚基)在启动子远端位点产生的DNase I保护图谱(“足迹”)比糖皮质激素受体产生的更长。启动子远端结合位点的甲基化保护研究确定了鸡孕激素受体的四个接触点和糖皮质激素受体的三个接触点,其中只有一个接触点为两者共有。计算机图形模型使人们能够设想每个受体与DNA双螺旋B型的不同相互作用方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0389/323397/e3421faa5a33/pnas00313-0048-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验