首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Oscillatory control of Delta-like1 in cell interactions regulates dynamic gene expression and tissue morphogenesis
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Oscillatory control of Delta-like1 in cell interactions regulates dynamic gene expression and tissue morphogenesis

机译:Delta-like1在细胞相互作用中的振荡控制调节动态基因表达和组织形态发生。

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摘要

Notch signaling regulates tissue morphogenesis through cell-cell interactions. The Notch effectors Hes1 and Hes7 are expressed in an oscillatory manner and regulate developmental processes such as neurogenesis and somitogenesis, respectively. Expression of the mRNA for the mouse Notch ligand Delta-like1 (Dll1) is also oscillatory. However, the dynamics of Dll1 protein expression are controversial, and their functional significance is unknown. Here, we developed a live-imaging system and found that Dll1 protein expression oscillated in neural progenitors and presomitic mesoderm cells. Notably, when Dll1 expression was accelerated or delayed by shortening or elongating the Dll1 gene, Dll1 oscillations became severely dampened or quenched at intermediate levels, as modeled mathematically. Under this condition, Hes1 and Hes7 oscillations were also dampened. In the presomitic mesoderm, steady Dll1 expression led to severe fusion of somites and their derivatives, such as vertebrae and ribs. In the developing brain, steady Dll1 expression inhibited proliferation of neural progenitors and accelerated neurogenesis, whereas optogenetic induction of Dll1 oscillation efficiently maintained neural progenitors. These results indicate that the appropriate timing of Dll1 expression is critical for the oscillatory networks and suggest the functional significance of oscillatory cell-cell interactions in tissue morphogenesis.
机译:Notch信号通过细胞间相互作用调节组织形态发生。 Notch效应子Hes1和Hes7以振荡方式表达,并分别调节发育过程,例如神经发生和体发生。小鼠Notch配体Delta-like1(Dll1)的mRNA表达也具有振荡性。但是,Dll1蛋白表达的动力学是有争议的,其功能的意义是未知的。在这里,我们开发了一个实时成像系统,并发现Dll1蛋白表达在神经祖细胞和早熟中胚层细胞中振荡。值得注意的是,当通过缩短或延长Dll1基因来加速或延迟Dll1表达时,Dll1振荡会在中等水平上严重减弱或淬灭,如数学模型所示。在这种情况下,Hes1和Hes7的振荡也被衰减。在早熟的中胚层中,稳定的Dll1表达导致体节及其衍生物(如椎骨和肋骨)的严重融合。在发育中的大脑中,稳定的Dll1表达抑制神经祖细胞的增殖并加速神经发生,而Dll1振荡的光遗传诱导有效地维持了神经祖细胞。这些结果表明,Dll1表达的适当时机对于振荡网络至关重要,并暗示了振荡细胞间相互作用在组织形态发生中的功能意义。

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