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Published on: March 13, 2015
GAGA Regulates Border Cell Migration in Drosophila
Anna A Ogienko1, Lyubov A Yarinich1,2, Elena V Fedorova3
1Department of the Regulation of Genetic Processes, Institute of Molecular and Cellular Biology of the Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russia.
The GAGA transcription factor, encoded by the Trithorax-like (Trl) gene, is crucial for border cell migration during Drosophila oogenesis. Trl mutations impair migration, partly by reducing slow border cells (slbo) expression, suggesting GAGA directly regulates slbo.
Area of Science:
- Developmental Biology
- Cell Biology
- Genetics
Background:
- Collective cell migration is vital for development and disease.
- Border cell migration in Drosophila oogenesis is a key model for studying collective cell movement.
- The slow border cells (slbo) gene product is essential for border cell migration, but its regulation is not fully understood.
Purpose of the Study:
- To investigate the role of the Trithorax-like (Trl) gene and its encoded GAGA transcription factor in Drosophila border cell migration.
- To determine if GAGA directly regulates the slow border cells (slbo) gene.
Main Methods:
- Analysis of border cell migration in Trl mutant Drosophila.
- Examination of slbo gene expression levels in Trl mutants.
- Genetic interaction studies between Trl and slbo mutants.
- Reporter gene assays to assess GAGA binding to the slbo promoter/enhancer.
Main Results:
- Trl mutations significantly disrupt border cell migration.
- slbo expression is reduced in Trl mutant border cells.
- Evidence suggests GAGA directly binds to and regulates the slbo gene.
- Overexpression of slbo cannot fully rescue Trl mutant migration defects, indicating other GAGA targets are involved.
Conclusions:
- GAGA, a transcription factor encoded by Trl, is a novel and important regulator of collective cell migration in Drosophila oogenesis.
- GAGA's regulation of slbo is a key mechanism, but other GAGA targets also contribute to border cell migration.
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