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首页> 外文期刊>Development >Thorax closure in Drosophila: involvement of Fos and the JNK pathway.
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Thorax closure in Drosophila: involvement of Fos and the JNK pathway.

机译:果蝇的胸部封闭:Fos和JNK通路的参与。

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摘要

Dorsal closure, a morphogenetic movement during Drosophila embryogenesis, is controlled by the Drosophila JNK pathway, D-Fos and the phosphatase Puckered (Puc). To identify principles of epithelial closure processes, we studied another cell sheet movement that we term thorax closure, the joining of the parts of the wing imaginal discs which give rise to the adult thorax during metamorphosis. In thorax closure a special row of margin cells express puc and accumulate prominent actin fibres during midline attachment. Genetic data indicate a requirement of D-Fos and the JNK pathway for thorax closure, and a negative regulatory role of Puc. Furthermore, puc expression co-localises with elevated levels of D-Fos, is reduced in a JNK or D-Fos loss-of-function background and is ectopically induced after JNK activation. This suggests that Puc acts downstream of the JNK pathway and D-Fos to mediate a negative feed-back loop. Therefore, the molecular circuitry required for thorax closure is very similar to the one directing dorsal closure in the embryo, even though the tissues are not related. This finding supports the hypothesis that the mechanism controlling dorsal closure has been co-opted for thorax closure in the evolution of insect metamorphosis and may represent a more widely used functional module for tissue closure in other species as well.
机译:背闭合是果蝇胚胎发生过程中的形态发生运动,受果蝇JNK途径,D-Fos和磷酸化酶(Puc)控制。为了确定上皮闭合过程的原理,我们研究了另一种被称为胸腔闭合的细胞片运动,即机翼假想椎间盘各部分的结合,在变态过程中形成了成年胸腔。在胸腔闭合过程中,一排特殊的边缘细胞表达puc并在中线附着过程中积聚突出的肌动蛋白纤维。遗传数据表明需要D-Fos和JNK途径来封闭胸腔,而Puc的负调控作用。此外,puc表达与高水平的D-Fos共定位,在JNK或D-Fos功能丧失的背景下降低,并且在JNK激活后被异位诱导。这表明Puc在JNK途径和D-Fos的下游起作用,以介导负反馈回路。因此,即使组织不相关,胸腔闭合所需的分子电路也与指导胚胎背侧闭合的分子电路非常相似。这一发现支持以下假设:在昆虫变态的进化过程中,控制背侧闭合的机制已被选择用于胸腔闭合,并且可能代表了其他物种中组织闭合的更广泛使用的功能模块。

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