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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Noncanonical Decapentaplegic Signaling Activates Matrix Metalloproteinase 1 To Restrict Hedgehog Activity and Limit Ectopic Eye Differentiation in Drosophila
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Noncanonical Decapentaplegic Signaling Activates Matrix Metalloproteinase 1 To Restrict Hedgehog Activity and Limit Ectopic Eye Differentiation in Drosophila

机译:非规范性的去色散性信号激活基质金属蛋白酶1来限制刺猬活性和限制果蝇的异位眼分化。

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摘要

One of the pertinent issues associated with cellular plasticity is to understand how the delicate balance between the determined state of cells and the extent to which they can transdetermine is maintained. Employing the well-established model of generating ectopic eyes in developing wing discs of Drosophila by ectopic [eyeless][1] expression, we provide evidence for the genetic basis of this mechanism. By both loss-of-function and gain-of-function genetic analyses, we demonstrate that Matrix metalloproteinase 1 (Mmp1) plays an important role in regulating the extent of ectopic ommatidial differentiation. Transcriptional activation of ectopic Mmp1 by the morphogen Decapentaplegic (Dpp) is not triggered by its canonical signaling pathway which involves Mad. Rather, Dpp activates an alternate cascade involving dTak1 and JNK, to induce ectopic Mmp1 expression. Mutational analyses reveal that Mmp1 negatively regulates ectopic eye differentiation by restricting the rate of proliferation and the levels of expression of retinal-determining genes [dachshund][2] and [eyes absent][3] . This is primarily achieved by restricting the range of Hedgehog (Hh) signaling. Importantly, the increase in proliferation and upregulation of target retinal-determining genes, as observed upon attenuating Mmp1 activity, gets significantly rescued when ectopic eyes are generated in wing discs of [hh][4] heterozygous mutants. In conjunction with the previously established instructive and permissive roles of Dpp in facilitating ectopic eye differentiation in wing discs, the outcome of this study sheds light on a mechanism by which Dpp plays a dual role in modulating the delicate balance between the determined state of cells and the extent they can transdetermine. [1]: http://flybase.org/reports/FBgn0005558.html [2]: http://flybase.org/reports/FBgn0005677.html [3]: http://flybase.org/reports/FBgn0000320.html [4]: http://flybase.org/reports/FBgn0004644.html
机译:与细胞可塑性有关的相关问题之一是要了解如何维持所确定的细胞状态与它们可以转决定的程度之间的微妙平衡。利用成熟的通过异位[eyeless] [1]表达在果蝇发育中的盘状翼中生成异位眼的模型,我们为该机制的遗传基础提供了证据。通过功能丧失和功能获得的遗传分析,我们证明基质金属蛋白酶1(Mmp1)在调节异位生殖细胞分化程度中起重要作用。形态发生剂Decapentaplegic(Dpp)对异位Mmp1的转录激活不是由其涉及Mad的经典信号通路触发的。而是,Dpp激活涉及dTak1和JNK的另一级联反应,以诱导异位Mmp1表达。突变分析显示,Mmp1通过限制视网膜决定基因[Dachshund] [2]和[缺少眼睛] [3]的增殖速率和表达水平来负调控异位眼的分化。这主要是通过限制刺猬(Hh)信号的范围来实现的。重要的是,当[hh] [4]杂合子突变体的翼状盘中产生异位眼时,如减弱Mmp1活性所观察到的,靶视网膜决定基因的增殖和上调的增加得到了明显的挽救。结合先前确定的Dpp在促进翼片异位眼分化中的指导和放任性作用,这项研究的结果阐明了Dpp在调节确定的细胞状态和细胞状态之间的微妙平衡中起双重作用的机制。他们可以确定的程度。 [1]:http://flybase.org/reports/FBgn0005558.html [2]:http://flybase.org/reports/FBgn0005677.html [3]:http://flybase.org/reports/FBgn0000320。 html [4]:http://flybase.org/reports/FBgn0004644.html

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