首页> 美国卫生研究院文献>The EMBO Journal >The bx region enhancer a distant cis-control element of the Drosophila Ubx gene and its regulation by hunchback and other segmentation genes.
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The bx region enhancer a distant cis-control element of the Drosophila Ubx gene and its regulation by hunchback and other segmentation genes.

机译:bx区域增强子是果蝇Ubx基因的一个遥远的顺式控制元件由驼背和其他分段基因调控。

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摘要

The Drosophila homeotic gene Ultrabithorax (Ubx) is regulated by complex mechanisms that specify the spatial domain, the timing and the activity of the gene in individual tissues and in individual cells. In early embryonic development, Ubx expression is controlled by segmentation genes turned on earlier in the developmental hierarchy. Correct Ubx expression depends on multiple regulatory sequences located outside the basal promoter. Here we report that a 500 bp DNA fragment from the bx region of the Ubx unit, approximately 30 kb away from the promoter, contains one of the distant regulatory elements (bx region enhancer, BRE). During early embryogenesis, this enhancer element activates the Ubx promoter in parasegments (PS) 6, 8, 10, and 12 and represses it in the anterior half of the embryo. The repressor of the anterior Ubx expression is the gap gene hunchback (hb). We show that the hb protein binds to the BRE element and that such binding is essential for hb repression in vivo, hb protein also binds to DNA fragments from abx and bxd, two other regulatory regions of the Ubx gene. We conclude that hb represses Ubx expression directly by binding to BRE and probably other Ubx regulatory elements. In addition, the BRE pattern requires input from other segmentation genes, among them tailless and fushi tarazu but not Krüppel and knirps.
机译:果蝇同源基因Ultrabithorax(Ubx)由复杂的机制调控,这些机制指定了基因在单个组织和单个细胞中的空间结构,时间和活动。在早期胚胎发育中,Ubx表达受发育层次中较早开启的分割基因控制。正确的Ubx表达取决于位于基础启动子外部的多个调控序列。在这里我们报告说,距Ubx单元bx区域约500 bp的500 bp DNA片段距启动子约30 kb,其中包含一个遥远的调控元件(bx区域增强子,BRE)。在早期胚胎发生过程中,这种增强子元件会激活节段(PS)6、8、10和12中的Ubx启动子,并在胚胎的前半部抑制它。 Ubx前表达的阻遏物是缺口基因驼背(hb)。我们表明,hb蛋白与BRE元素结合,并且这种结合对于体内hb抑制是必不可少的,hb蛋白还与abx和bxd(Ubx基因的其他两个调控区域)的DNA片段结合。我们得出的结论是,血红蛋白通过与BRE和其他可能的Ubx调控元件结合而直接抑制Ubx表达。另外,BRE模式需要来自其他分割基因的输入,其中包括无尾和富士tarazu,而不需要Krüppel和knirps。

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