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Systematic analysis of the transcriptional switch inducing migration of border cells.


ABSTRACT: Cell migration within a natural context is tightly controlled, often by specific transcription factors. However, the switch from stationary to migratory behavior is poorly understood. Border cells perform a spatially and temporally controlled invasive migration during Drosophila oogenesis. Slbo, a C/EBP family transcriptional activator, is required for them to become migratory. We purified wild-type and slbo mutant border cells as well as nonmigratory follicle cells and performed comparative whole-genome expression profiling, followed by functional tests of the contributions of identified targets to migration. About 300 genes were significantly upregulated in border cells, many dependent on Slbo. Among these, the microtubule regulator Stathmin was strongly upregulated and was required for normal migration. Actin cytoskeleton regulators were also induced, including, surprisingly, a large cluster of "muscle-specific" genes. We conclude that Slbo induces multiple cytoskeletal effectors, and that each contributes to the behavioral changes in border cells.

SUBMITTER: Borghese L 

PROVIDER: S-EPMC2955450 | biostudies-literature | 2006 Apr

REPOSITORIES: biostudies-literature

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Systematic analysis of the transcriptional switch inducing migration of border cells.

Borghese Lodovica L   Fletcher Georgina G   Mathieu Juliette J   Atzberger Ann A   Eades William C WC   Cagan Ross L RL   Rørth Pernille P  

Developmental cell 20060401 4


Cell migration within a natural context is tightly controlled, often by specific transcription factors. However, the switch from stationary to migratory behavior is poorly understood. Border cells perform a spatially and temporally controlled invasive migration during Drosophila oogenesis. Slbo, a C/EBP family transcriptional activator, is required for them to become migratory. We purified wild-type and slbo mutant border cells as well as nonmigratory follicle cells and performed comparative who  ...[more]

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