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果蝇胚胎中一个dpp靶基因的调控

Regulation of a dpp target gene in the Drosophila embryo.

作者信息

Rusch J, Levine M

机构信息

Department of Biology, UCSD, La Jolla, CA 92093-0357, USA.

出版信息

Development. 1997 Jan;124(2):303-11. doi: 10.1242/dev.124.2.303.

Abstract

In Drosophila, two TGF-beta growth factors, dpp and screw, function synergistically to subdivide the dorsal ectoderm into two embryonic tissues, the amnioserosa and dorsal epidermis. Previous studies have shown that peak dpp activity is required for the localized expression of zerknüllt (zen), which encodes a homeodomain transcription factor. We present evidence that zen directly activates the amnioserosa-specific expression of a downstream target gene, Race (Related to angiotensin converting enzyme). A 533 bp enhancer from the Race promoter region is shown to mediate selective expression in the amnioserosa, as well as the anterior and posterior midgut rudiments. This enhancer contains three zen protein binding sites, and mutations in these sites virtually abolish the expression of an otherwise normal Race-lacZ fusion gene in the amnioserosa, but not in the gut. Genetic epistasis experiments suggest that zen is not the sole activator of Race, although a hyperactivated form of zen (a zen-VP16 fusion protein) can partially complement reduced levels of dpp activity. These results suggest that dpp regulates multiple transcription factors, which function synergistically to specify the amnioserosa.

摘要

在果蝇中,两种转化生长因子β(TGF-β),即dpp和screw,协同作用将背侧外胚层细分为两种胚胎组织,即羊膜浆膜和背侧表皮。先前的研究表明,zerknüllt(zen)基因的定位表达需要dpp活性达到峰值,zen基因编码一种同源结构域转录因子。我们提供的证据表明,zen直接激活下游靶基因Race(与血管紧张素转换酶相关)在羊膜浆膜中的特异性表达。来自Race启动子区域的一个533 bp增强子被证明可介导在羊膜浆膜以及前后中肠原基中的选择性表达。该增强子包含三个zen蛋白结合位点,这些位点的突变几乎消除了原本正常的Race-lacZ融合基因在羊膜浆膜中的表达,但在肠道中却没有。遗传上位性实验表明,zen并非Race的唯一激活因子,尽管一种超激活形式的zen(zen-VP16融合蛋白)可以部分弥补dpp活性降低的情况。这些结果表明,dpp调节多种转录因子,这些转录因子协同作用以确定羊膜浆膜的特征。

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