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The Salvador/Warts/Hippo pathway controls regenerative tissue growth in Drosophila melanogaster.

机译:Salvador / Warts / Hippo通路控制果蝇的再生组织生长。

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During tissue regeneration, cell proliferation replaces missing structures to restore organ function. Regenerative potential differs greatly between organs and organisms; for example some amphibians can regrow entire limbs whereas mammals cannot. The process of regeneration relies on several signaling pathways that control developmental tissue growth, and implies the existence of organ size-control checkpoints that regulate both developmental, and regenerative, growth. Here we explore the role of one such checkpoint, the Salvador-Warts-Hippo pathway, in tissue regeneration. The Salvador-Warts-Hippo pathway limits tissue growth by repressing the Yorkie transcriptional co-activator. Several proteins serve as upstream modulators of this pathway including the atypical cadherins, Dachsous and Fat, whilst the atypical myosin, Dachs, functions downstream of Fat to activate Yorkie. Using Drosophila melanogaster imaginal discs we show that Salvador-Warts-Hippo pathway activity is repressed in regenerating tissue and that Yorkie is rate-limiting for regeneration of the developing wing. We show that regeneration is compromised in dachs mutant wing discs, but that proteins in addition to Fat and Dachs are likely to modulate Yorkie activity in regenerating cells. In conclusion our data reveal the importance of Yorkie hyperactivation for tissue regeneration and suggest that multiple upstream inputs, including Fat-Dachsous signaling, sense tissue damage and regulate Yorkie activity during regeneration of epithelial tissues.
机译:在组织再生过程中,细胞增殖会替换缺失的结构以恢复器官功能。器官和生物体之间的再生潜力差异很大。例如,某些两栖动物可以使整个肢体再生,而哺乳动物则不能。再生过程依赖于控制发育组织生长的几种信号传导途径,并暗示着调节发育和再生生长的器官大小控制检查点的存在。在这里,我们探讨了一种这样的检查点,萨尔瓦多-瓦尔特-河马途径,在组织再生中的作用。 Salvador-Warts-Hippo途径通过抑制Yorkie转录共激活因子来限制组织的生长。几种蛋白质充当该途径的上游调节剂,包括非典型钙黏着蛋白Dachsous和Fat,而非典型肌球蛋白Dachs在脂肪的下游起作用以激活Yorkie。使用果蝇黑色素瘤假想光盘,我们显示Salvador-Warts-Hippo通路的活性在再生组织中受到抑制,而Yorkie则在发育中的机翼的再生中受到速率限制。我们表明,再生在达克斯突变体翼盘中受到损害,但是除了脂肪和达克斯之外,蛋白质还可能在再生细胞中调节约克活性。总之,我们的数据揭示了Yorkie过度活化对于组织再生的重要性,并表明多个上游输入,包括脂肪-Dachsous信号传导,感知组织损伤并在上皮组织再生期间调节Yorkie活性。

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