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Unmasking Activation of the Zygotic Genome Using Chromosomal Deletions in the Drosophila Embryo

机译:利用果蝇胚胎中的染色体缺失揭示合子基因组的激活。

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摘要

During the maternal-to-zygotic transition, a developing embryo integrates post-transcriptional regulation of maternal mRNAs with transcriptional activation of its own genome. By combining chromosomal ablation in Drosophila with microarray analysis, we characterized the basis of this integration. We show that the expression profile for at least one third of zygotically active genes is coupled to the concomitant degradation of the corresponding maternal mRNAs. The embryo uses transcription and degradation to generate localized patterns of expression, and zygotic transcription to degrade distinct classes of maternal transcripts. Although degradation does not appear to involve a simple regulatory code, the activation of the zygotic genome starts from intronless genes sharing a common cis-element. This cis-element interacts with a single protein, the Bicoid stability factor, and acts as a potent enhancer capable of timing the activity of an exogenous transactivator. We propose that this regulatory mode links morphogen gradients with temporal regulation during the maternal-to-zygotic transition.
机译:在母体向合子的过渡过程中,发育中的胚胎将母体mRNA的转录后调控与自身基因组的转录激活整合在一起。通过结合果蝇中的染色体消融与微阵列分析,我们表征了这种整合的基础。我们表明,至少三分之一的合子活性基因的表达谱与相应的母体mRNA的伴随降解偶联。胚胎利用转录和降解产生局部表达模式,并利用合子转录降解不同类别的母本转录本。尽管降解似乎不涉及简单的调控密码,但合子基因组的激活始于共享相同顺式元件的无内含子基因。该顺式元素与单一蛋白(双环类稳定因子)相互作用,并充当有效的增强剂,能够定时外源反式激活因子的活性。我们提出,这种调节模式在母亲到合子的过渡过程中将形态发生子梯度与时间调节联系起来。

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