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首页> 外文期刊>Development >smoothened and thickveins regulate Moleskin/Importin 7-mediated MAP kinase signaling in the developing Drosophila eye.
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smoothened and thickveins regulate Moleskin/Importin 7-mediated MAP kinase signaling in the developing Drosophila eye.

机译:在发育中的果蝇眼中,平滑和增稠的蛋白调节着Moleskin / Importin 7介导的MAP激酶信号传导。

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摘要

The Drosophila Mitogen Activated Protein Kinase (MAPK) Rolled is a key regulator of developmental signaling, relaying information from the cytoplasm into the nucleus. Cytoplasmic MEK phosphorylates MAPK (pMAPK), which then dimerizes and translocates to the nucleus where it regulates transcription factors. In cell culture, MAPK nuclear translocation directly follows phosphorylation, but in developing tissues pMAPK can be held in the cytoplasm for extended periods (hours). Here, we show that Moleskin antigen (Drosophila Importin 7/Msk), a MAPK transport factor, is sequestered apically at a time when lateral inhibition is required for patterning in the developing eye. We suggest that this apical restriction of Msk limits MAPK nuclear translocation and blocks Ras pathway nuclear signaling. Ectopic expression of Msk overcomes this block and disrupts patterning. Additionally, the MAPK cytoplasmic hold is genetically dependent on the presence of Decapentaplegic (Dpp) and Hedgehog receptors.
机译:果蝇的丝裂原丝裂原活化蛋白激酶(MAPK)是发育信号的关键调节剂,可将信息从细胞质传递到细胞核中。细胞质MEK会磷酸化MAPK(pMAPK),然后将其二聚化并转运至细胞核,从而调节转录因子。在细胞培养中,MAPK核易位直接跟随磷酸化作用,但在发育中的组织中,pMAPK可以在细胞质中保留较长时间(数小时)。在这里,我们显示出在需要侧向抑制才能在发育中的眼中形成图案时,将MAPK转运因子Moleskin抗原(果蝇Importin 7 / Msk)隔离开。我们建议,Msk的这种顶端限制限制MAPK核易位,并阻止Ras途径核信号传导。 Msk的异位表达克服了这一障碍并破坏了模式。另外,MAPK的细胞质保留在遗传上取决于十足瘫痪(Dpp)和刺猬受体的存在。

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