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The Torso signaling pathway modulates a dual transcriptional switch to regulate tailless expression

机译:躯干信号通路调节双重转录开关,以调节无尾表达

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The Torso (Tor) signaling pathway activates tailless (tll) expression by relieving tll repression. None of the repressors identified so far, such as Capicuo, Groucho and Tramtrack69 (Ttk69), bind to the tor response element (tor-RE) or fully elucidate tll repression. In this study, an expanded tll expression pattern was shown in embryos with reduced heat shock factor (hsf) and Trithorax-like (Trl) activities. The GAGA factor, GAF encoded by Trl, bound weakly to the tor-RE, and this binding was enhanced by both Hsf and Ttk69. A similar extent of expansion of tll expression was observed in embryos with simultaneous knockdown of hsf, Trl and ttk69 activities, and in embryos with constitutively active Tor. Hsf is a substrate of mitogen-activated protein kinase and S378 is the major phosphorylation site. Phosphorylation converts Hsf from a repressor to an activator that works with GAF to activate tll expression. In conclusion, the GAF/Hsf/Ttk69 complex binding to the tor-RE remodels local chromatin structure to repress tll expression and the Tor signaling pathway activate tll expression by modulating a dual transcriptional switch.
机译:躯干(Tor)信号通路通过缓解tll抑制来激活无尾(tll)表达。到目前为止,没有发现任何阻遏物,例如Capicuo,Groucho和Tramtrack69(Ttk69),都不会与tor反应元件(tor-RE)结合或完全阐明tll抑制作用。在这项研究中,在具有降低的热休克因子(hsf)和类胸腺(Trl)活性的胚胎中显示了扩展的tll表达模式。由Trl编码的GAGA因子GAGA与tor-RE弱结合,而Hsf和Ttk69均增强了这种结合。在同时敲低hsf,Tr1和ttk69活性的胚胎以及具有组成型活性Tor的胚胎中,观察到了tll表达扩展的相似程度。 Hsf是促分裂原活化蛋白激酶的底物,S378是主要的磷酸化位点。磷酸化将Hsf从阻遏物转化为与GAF共同激活tll表达的激活物。总之,与tor-RE结合的GAF / Hsf / Ttk69复合体可重塑局部染色质结构,从而抑制tll表达,而Tor信号通路则通过调节双重转录开关来激活tll表达。

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