|Title||The transcription/migration interface in heart precursors of Ciona intestinalis.|
|Publication Type||Journal Article|
|Year of Publication||2008|
|Authors||Christiaen, L, Davidson, B, Kawashima, T, Powell, W, Nolla, H, Vranizan, K, Levine, M|
|Date Published||2008 Jun 6|
|Keywords||Actin Cytoskeleton, Animals, cdc42 GTP-Binding Protein, Cell Lineage, Cell Movement, Cell Surface Extensions, Ciona intestinalis, Fibroblast Growth Factors, Gene Expression Profiling, Gene Expression Regulation, Developmental, Gene Regulatory Networks, GTP Phosphohydrolases, Heart, Models, Animal, Morphogenesis, Muscle Cells, Myocardium, Oligonucleotide Array Sequence Analysis, Oligonucleotides, Antisense, Signal Transduction, Transcription, Genetic, Up-Regulation|
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.