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Two distinct mechanisms for differential positioning of gene expression borders involving the Drosophila gap protein giant.

机译:两个不同的机制涉及果蝇间隙蛋白巨人基因表达边界的差异定位。

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We have combined genetic experiments and a targeted misexpression approach to examine the role of the gap gene giant (gt) in patterning anterior regions of the Drosophila embryo. Our results suggest that gt functions in the repression of three target genes, the gap genes Kruppel (Kr) and hunchback (hb), and the pair-rule gene even-skipped (eve). The anterior border of Kr, which lies 4-5 nucleus diameters posterior to nuclei that express gt mRNA, is set by a threshold repression mechanism involving very low levels of gt protein. In contrast, gt activity is required, but not sufficient for formation of the anterior border of eve stripe 2, which lies adjacent to nuclei that express gt mRNA. We propose that gt's role in forming this border is to potentiate repressive interaction(s) mediated by other factor(s) that are also localized to anterior regions of the early embryo. Finally, gt is required for repression of zygotic hb expression in more anterior regions of the embryo. The differential responses of these target genes to gt repression are critical for the correct positioning and maintenance of segmentation stripes, and normal anterior development.
机译:我们已经结合了遗传实验和针对性的错误表达方法,以检查缺口基因巨人(gt)在果蝇胚胎前部区域模式中的作用。我们的研究结果表明,gt在抑制三个靶基因,空位基因Kruppel(Kr)和驼背(hb),以及成对规则基因(eve)的阻遏中起作用。 Kr的前边界位于表达gt mRNA的原子核后4-5个核直径,由阈值抑制机制设定,该机制涉及极低水平的gt蛋白质。相反,gt活性是必需的,但不足以形成前夕条纹2的前边界,其与表达gt mRNA的细胞核相邻。我们建议gt在形成此边界中的作用是增强由也定位于早期胚胎前部区域的其他因子介导的抑制性相互作用。最后,需要gt来抑制胚胎更多前部区域的合子hb表达。这些靶基因对gt抑制的差异反应对于正确定位和维持分割条带以及正常前发展至关重要。

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