首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Anterior-posterior Positional Information In The Absence Of A Strong Bicoid Gradient
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Anterior-posterior Positional Information In The Absence Of A Strong Bicoid Gradient

机译:在没有强双曲线梯度的情况下的前后位置信息

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The Bicoid (Bcd) transcription factor is distributed as a long-range concentration gradient along the anterior posterior (AP) axis of the Drosophila embryo. Bcd is required for the activation of a series of target genes, which are expressed at specific positions within the gradient. Here we directly tested whether different concentration thresholds within the Bcd gradient establish the relative positions of its target genes by flattening the gradient and systematically varying expression levels. Genome-wide expression profiles were used to estimate the total number of Bcd target genes, and a general correlation was found between the Bcd concentration required for activation and the positions where target genes are expressed in wild-type embryos. However, concentrations required for target gene activation in embryos with flattened Bcd were consistently lower than those present at each target gene's position in the wild-type gradient, suggesting that Bcd is in excess at every position along the AP axis. Also, several Bcd target genes were positioned in correctly ordered stripes in embryos with flattened Bcd, and we suggest that these stripes are normally regulated by interactions between Bcd and the terminal patterning system. Our findings argue strongly against the strict interpretation of the Bcd morphogen hypothesis, and support the idea that target gene positioning involves combinatorial interactions that are mediated by the binding site architecture of each gene's cis-regulatory elements.
机译:Bicoid(Bcd)转录因子沿果蝇胚胎的前后(AP)轴以远程浓度梯度分布。 Bcd是激活一系列靶基因所必需的,这些靶基因在梯度内的特定位置表达。在这里,我们直接测试了Bcd梯度内的不同浓度阈值是否通过使梯度变平和系统地改变表达水平来建立其靶基因的相对位置。全基因组表达谱用于估计Bcd靶基因的总数,并且发现激活所需的Bcd浓度与野生型胚胎中表达靶基因的位置之间存在一般相关性。然而,在扁平化Bcd胚胎中激活靶基因所需的浓度始终低于野生型梯度中每个靶基因位置上存在的浓度,这表明Bcd沿AP轴的每个位置都过量。另外,几个Bcd靶基因在Bcd变平的胚胎中以正确顺序排列在条带中,我们建议这些条带通常受Bcd与末端构图系统之间的相互作用调控。我们的发现强烈反对严格解释Bcd形态发生子假设,并支持靶基因定位涉及由每个基因的顺式调控元件的结合位点结构介导的组合相互作用的观点。

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