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果蝇 even skipped stripe 3+7 增强子的组合激活和浓度依赖性抑制。

Combinatorial activation and concentration-dependent repression of the Drosophila even skipped stripe 3+7 enhancer.

机构信息

Department of Biology, New York University, New York, NY 10003, USA.

出版信息

Development. 2011 Oct;138(19):4291-9. doi: 10.1242/dev.065987. Epub 2011 Aug 24.

Abstract

Despite years of study, the precise mechanisms that control position-specific gene expression during development are not understood. Here, we analyze an enhancer element from the even skipped (eve) gene, which activates and positions two stripes of expression (stripes 3 and 7) in blastoderm stage Drosophila embryos. Previous genetic studies showed that the JAK-STAT pathway is required for full activation of the enhancer, whereas the gap genes hunchback (hb) and knirps (kni) are required for placement of the boundaries of both stripes. We show that the maternal zinc-finger protein Zelda (Zld) is absolutely required for activation, and present evidence that Zld binds to multiple non-canonical sites. We also use a combination of in vitro binding experiments and bioinformatics analysis to redefine the Kni-binding motif, and mutational analysis and in vivo tests to show that Kni and Hb are dedicated repressors that function by direct DNA binding. These experiments significantly extend our understanding of how the eve enhancer integrates positive and negative transcriptional activities to generate sharp boundaries in the early embryo.

摘要

尽管经过多年的研究,控制发育过程中特定位置基因表达的精确机制仍未被理解。在这里,我们分析了来自 even skipped (eve) 基因的增强子元件,该元件在果蝇胚胎的胚胎期激活并定位两个表达条纹(条纹 3 和 7)。先前的遗传研究表明,JAK-STAT 途径是增强子完全激活所必需的,而间隙基因 hunchback (hb) 和 knirps (kni) 则是定位两个条纹边界所必需的。我们表明,母体锌指蛋白 Zelda (Zld) 对于激活是绝对必需的,并提供了 Zld 结合多个非典型位点的证据。我们还使用体外结合实验和生物信息学分析的组合重新定义了 Kni 结合基序,并通过突变分析和体内测试表明 Kni 和 Hb 是专门的抑制剂,通过直接 DNA 结合起作用。这些实验极大地扩展了我们对 eve 增强子如何整合正转录活性和负转录活性以在早期胚胎中产生锐利边界的理解。

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