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通过转基因技术确定的内耳感觉细胞特异性启动子。

A specific promoter of the sensory cells of the inner ear defined by transgenesis.

作者信息

Boëda B, Weil D, Petit C

机构信息

Unité de Génétique des Déficits Sensoriels, CNRS URA 1968, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France.

出版信息

Hum Mol Genet. 2001 Jul 15;10(15):1581-9. doi: 10.1093/hmg/10.15.1581.

Abstract

To date, no promoter sequence specific to the inner ear sensory cells (hair cells) has been reported. In an effort to understand the molecular mechanisms that determine hair cell fate in the inner ear, and with the goal of developing a valuable tool for gene therapy and for the generation of conditional knockouts, we initiated a search for cis-acting DNA sequences that regulate the expression of the murine Myo7a and human MYO7A genes. These genes encode the unconventional myosin VIIA which is expressed in hair cells and in some other epithelial cells. We generated lines of transgenic mice expressing the green fluorescent protein (GFP ) reporter gene under the control of several 5'-truncated versions of the Myo7a/MYO7A promoter region and intron 1. We obtained transgenic mice with a GFP expression restricted to the hair cells of the inner ear, cochlea and vestibule. Successive deletions of the promoter allowed us to define a minimal sequence of 118 bp that is sufficient, in the presence of intron 1, to target the transgene expression to hair cells. In addition, the deletion of intron 1 from the transgenes abolished hair cell expression, thus indicating the presence of a strong enhancer in the intron. This is the first report of regulatory sequences sufficient to target the expression of a gene exclusively in sensory cells of the inner ear. It also opens up the possibility for the analysis of the hair cell transcriptome.

摘要

迄今为止,尚未有内耳感觉细胞(毛细胞)特异性的启动子序列被报道。为了理解决定内耳毛细胞命运的分子机制,并为基因治疗和条件性基因敲除的产生开发一种有价值的工具,我们开始寻找调控小鼠Myo7a和人类MYO7A基因表达的顺式作用DNA序列。这些基因编码非常规肌球蛋白VIIA,其在内耳毛细胞和其他一些上皮细胞中表达。我们构建了在Myo7a/MYO7A启动子区域和内含子1的几个5'端截短版本控制下表达绿色荧光蛋白(GFP)报告基因的转基因小鼠品系。我们获得了GFP表达仅限于内耳、耳蜗和前庭毛细胞的转基因小鼠。启动子的连续缺失使我们能够确定一个118 bp的最小序列,该序列在存在内含子1的情况下足以将转基因表达靶向毛细胞。此外,从转基因中删除内含子1消除了毛细胞表达,从而表明内含子中存在一个强增强子。这是关于足以将基因表达专门靶向内耳感觉细胞的调控序列的首次报道。它也为毛细胞转录组的分析开辟了可能性。

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