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Signaling by the TGF-beta homolog decapentaplegic functions reiteratively within the network of genes controlling retinal cell fate determination in Drosophila.

机译:在果蝇中,通过控制视网膜细胞命运测定的基因网络中的TGF-β同源物decapentaplegic功能进​​行信号传导。

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Retinal cell fate determination in Drosophila is controlled by an interactive network of genes, including eyeless, eyes absent, sine oculis and dachshund. We have investigated the role of the TGF-beta homolog decapentaplegic in this pathway. We demonstrate that, during eye development, while eyeless transcription does not depend on decapentaplegic activity, the expression of eyes absent, sine oculis and dachshund are greatly reduced in a decapentaplegic mutant background. We also show that decapentaplegic signaling acts synergistically with and at multiple levels of the retinal determination network to induce eyes absent, sine oculis and dachshund expression and ectopic eye formation. These results suggest a mechanism by which a general patterning signal such as Decapentaplegic cooperates reiteratively with tissue-specific factors to determine distinct cell fates during development.
机译:果蝇中视网膜细胞命运的确定是由一个互动的基因网络控制的,这些基因包括无眼,无眼,正弦和腊肠。我们已经研究了TGF-β同源decapentaplegic在这一途径中的作用。我们证明,在眼睛发育过程中,尽管无眼转录不依赖于十足功能的活动,但在十足功能的突变体背景下,缺失的眼睛,正弦骨和腊肠的表情大大减少了。我们还显示,去眼睑功能障碍信号与视网膜测定网络并在其的多个水平上协同作用,以诱导不存在的眼睛,正弦眼和腊肠表达以及异位眼的形成。这些结果表明了一种机制,通过该机制,诸如Decapentaplegic之类的常规模式信号与组织特异性因子反复协作,以确定发育过程中的不同细胞命运。

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