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A Wingless and Notch double-repression mechanism regulates G1–S transition in the Drosophila wing

机译:无翼和缺口双重抑制机制调节果蝇翼中的G1–S过渡

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摘要

The control of tissue growth and patterning is orchestrated in various multicellular tissues by the coordinated activity of the signalling molecules Wnt/Wingless (Wg) and Notch, and mutations in these pathways can cause cancer. The role of these molecules in the control of cell proliferation and the crosstalk between their corresponding pathways remain poorly understood. Crosstalk between Notch and Wg has been proposed to organize pattern and growth in the Drosophila wing primordium. Here we report that Wg and Notch act in a surprisingly linear pathway to control G1–S progression. We present evidence that these molecules exert their function by regulating the expression of the dmyc proto-oncogene and the bantam micro-RNA, which positively modulated the activity of the E2F transcription factor. Our results demonstrate that Notch acts in this cellular context as a repressor of cell-cycle progression and Wg has a permissive role in alleviating Notch-mediated repression of G1–S progression in wing cells.
机译:通过信号分子Wnt / Wingless(Wg)和Notch的协调活性,在各种多细胞组织中对组织生长和模式的控制得以协调,这些途径中的突变会导致癌症。这些分子在控制细胞增殖和其相应途径之间的串扰中的作用仍然知之甚少。已经提出了Notch和Wg之间的串扰来组织果蝇翅原基的模式和生长。在这里,我们报道Wg和Notch以令人惊讶的线性途径来控制G1–S的进程。我们目前的证据表明,这些分子通过调节dmyc原癌基因和矮脚鸡微RNA的表达来发挥其功能,从而积极调节E2F转录因子的活性。我们的结果表明,Notch在这种细胞环境中起着抑制细胞周期进程的作用,而Wg在减轻Notch介导的机翼细胞对G1-S进程的阻遏中起着宽松的作用。

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