Suppr超能文献

Sp-1在滋养层细胞分化过程中对Id-1基因调控的参与。

Involvement of Sp-1 in the regulation of the Id-1 gene during trophoblast cell differentiation.

作者信息

Takeda T, Sakata M, Isobe A, Yamamoto T, Nishimoto F, Minekawa R, Hayashi M, Okamoto Y, Desprez P-Y, Tasaka K, Murata Y

机构信息

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

Placenta. 2007 Feb-Mar;28(2-3):192-8. doi: 10.1016/j.placenta.2006.03.002. Epub 2006 Apr 25.

Abstract

Id-1, a member of the helix-loop-helix transcription factor family, inhibits the differentiation of Rcho-1 cells, which were derived from rat choriocarcinoma and consist of trophoblast stem cells. Id-1 is expressed at a high level in undifferentiated trophoblast stem cells and then down-regulated during early differentiation, and is thought to be a key regulator in the trophoblast giant-cell differentiation pathway. In this study, we analyzed the signaling mechanism regulating the high expression levels of Id-1 in undifferentiated Rcho-1 cells. Promoter deletion analysis revealed that a 31-bp sequence (Box-2 region), located between -200 and -169bp in the Id-1 promoter is necessary for the promoter activity. Electrophoretic mobility shift assays and DNA affinity precipitation assays showed that Box-2-binding activity was decreased during differentiation and that Sp-1 protein bound to this sequence. The protein level of Sp-1 was decreased during the differentiation. These results suggest that the Sp-1 protein level may regulate the Box-2-binding activity and the trophoblast giant-cell differentiation.

摘要

Id-1是螺旋-环-螺旋转录因子家族的成员之一,可抑制Rcho-1细胞的分化,Rcho-1细胞源自大鼠绒毛膜癌,由滋养层干细胞组成。Id-1在未分化的滋养层干细胞中高水平表达,然后在早期分化过程中下调,被认为是滋养层巨细胞分化途径中的关键调节因子。在本研究中,我们分析了调节未分化Rcho-1细胞中Id-1高表达水平的信号传导机制。启动子缺失分析表明,Id-1启动子中位于-200至-169bp之间的31bp序列(Box-2区域)对于启动子活性是必需的。电泳迁移率变动分析和DNA亲和沉淀分析表明,Box-2结合活性在分化过程中降低,并且Sp-1蛋白与该序列结合。Sp-1的蛋白水平在分化过程中降低。这些结果表明,Sp-1蛋白水平可能调节Box-2结合活性和滋养层巨细胞分化。

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