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响应母体尾端和合子knirps活性而激活后部成对规则条纹表达。

Activation of posterior pair-rule stripe expression in response to maternal caudal and zygotic knirps activities.

作者信息

Häder T, La Rosée A, Ziebold U, Busch M, Taubert H, Jäckle H, Rivera-Pomar R

机构信息

Abteilung Molekulare Entwicklungsbiologie, Max-Planck-Institut für biophysikalische Chemie, D-37070, Göttingen, Germany.

出版信息

Mech Dev. 1998 Feb;71(1-2):177-86. doi: 10.1016/s0925-4773(98)00014-8.

Abstract

Drosophila pair-rule gene expression, in an array of seven evenly spaced stripes along the anterior-posterior axis of the blastoderm embryo, is controlled by distinct cis-acting stripe elements. In the anterior region, such elements mediate transcriptional activation in response to the maternal concentration gradient of the anterior determinant BICOID and repression by spatially distinct activities of zygotic gap genes. In the posterior region, activation of hairy stripe 6 has been shown to depend on the activity of the gap gene knirps, suggesting that posterior stripe expression is exclusively controlled by zygotic regulators. Here we show that the zygotic activation of hairy stripe 6 expression is preceded by activation in response to maternal caudal activity. Thus, transcriptional activation of posterior stripe expression is likely to be controlled by maternal and zygotic factors as has been observed for anterior stripes. The results suggest that activation and the expression level mediated by the hairy stripe 6-element depend on the number of activator binding sites, likely to involve additive rather than synergistic interactions. We found an identical transacting factor requirement for hairy stripe 6 and 7 expression. The arrangement of the corresponding binding sites for the common factors involved in the control of the two stripes share a high degree of similarity, but some of the factors exert opposite regulatory functions within the two enhancer elements.

摘要

果蝇成对规则基因的表达,在囊胚胚胎前后轴上呈一系列七条均匀间隔的条纹状,由不同的顺式作用条纹元件控制。在前部区域,这些元件响应前部决定因子BICOID的母体浓度梯度介导转录激活,并受合子间隙基因在空间上不同活性的抑制。在后部区域,已表明毛状条纹6的激活依赖于间隙基因克尼普斯的活性,这表明后部条纹表达完全由合子调节因子控制。在这里我们表明,毛状条纹6表达的合子激活之前是对母体尾端活性的响应激活。因此,后部条纹表达的转录激活可能像前部条纹那样由母体和合子因子共同控制。结果表明,毛状条纹6元件介导的激活和表达水平取决于激活剂结合位点的数量,可能涉及加性而非协同相互作用。我们发现毛状条纹6和7的表达对反式作用因子有相同的需求。控制这两条条纹的共同因子的相应结合位点的排列具有高度相似性,但其中一些因子在两个增强子元件中发挥相反的调节功能。

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