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The Transcription/Migration Interface in Heart Precursors of Ciona intestinalis

机译:Ciona intestinalis心脏前体中的转录/迁移界面

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Gene regulatory networks direct the progressive determination of cell fate during embryogenesis, but how they control cell behavior during morphogenesis remains largely elusive. Cell sorting, microarrays, and targeted molecular manipulations were used to analyze cardiac cell migration in the ascidian Ciona intestinalis. The heart network regulates genes involved in most cellular activities required for migration, including adhesion, cell polarity, and membrane protrusions. We demonstrated that fibroblast growth factor signaling and the forkhead transcription factor FoxF directly upregulate the small guanosine triphosphatase RhoDF, which synergizes with Cdc42 to contribute to the protrusive activity of migrating cells. Moreover, RhoDF induces membrane protrusions independently of other cellular activities required for migration. We propose that transcription regulation of specific effector genes determines the coordinated deployment of discrete cellular modules underlying migration.
机译:基因调控网络指导着胚胎发育过程中细胞命运的逐步确定,但是在形态发生过程中它们如何控制细胞行为仍然难以捉摸。细胞分选,微阵列和靶向分子操作被用于分析海鞘Ciona intestinalis中的心脏细胞迁移。心脏网络调节参与迁移所需的大多数细胞活动的基因,包括粘附,细胞极性和膜突出。我们证明成纤维细胞生长因子信号和叉头转录因子FoxF直接上调小鸟苷三磷酸酶RhoDF,它与Cdc42协同作用,有助于迁移细胞的突出活性。此外,RhoDF诱导膜突起独立于迁移所需的其他细胞活动。我们建议特定效应基因的转录调控决定迁移背后的离散细胞模块的协调部署。

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