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在人类视网膜间视黄醇结合蛋白基因的视网膜特异性调控区域内鉴定出一个视网膜特异性足迹。

Identification of a retina-specific footprint within the retina-specific regulatory region of the human interphotoreceptor retinoid-binding protein gene.

作者信息

Liou G I, Matragoon S, Overbeek P A, Fei Y

机构信息

Department of Ophthalmology, Medical College of Georgia, Augusta 30912.

出版信息

Biochem Biophys Res Commun. 1994 Sep 30;203(3):1875-81. doi: 10.1006/bbrc.1994.2406.

Abstract

Regulation of the retina-specific expression of the interphotoreceptor retinoid-binding protein (IRBP) gene in transgenic mice requires sequences between nucleotide (nt) -156 and +19. DNAse I footprinting and electrophoretic mobility shift assays identified a region between nt -69 and -40 that interacts with some nuclear proteins from bovine and mouse retinas but not from a variety of other neural and non-neural tissues. The selectivity of this sequence to elicit IRBP promoter activity is indicated by their failure to bind some nuclear proteins following mutagenesis. Therefore, IRBP promoter activity is linked to nuclear protein binding at a regulatory motif between nt-69 and -40.

摘要

在转基因小鼠中,视网膜间视黄醇结合蛋白(IRBP)基因的视网膜特异性表达调控需要核苷酸(nt)-156至+19之间的序列。DNA酶I足迹法和电泳迁移率变动分析确定了nt -69至-40之间的一个区域,该区域与来自牛和小鼠视网膜的一些核蛋白相互作用,但不与多种其他神经和非神经组织的核蛋白相互作用。诱变后它们无法结合一些核蛋白,这表明该序列引发IRBP启动子活性具有选择性。因此,IRBP启动子活性与nt-69至-40之间调控基序处的核蛋白结合相关。

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