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Published on: July 10, 2018
Developmental effects of monensin on Drosophila melanogaster
Patrick Callaerts1, Arnold De Loof1
1Zoological Institute, Katholieke Universiteit Leuven, Naamsestraat 59, B-3000, Leuven, Belgium.
Abstract:
Extracellular matrix and membrane proteins and their correct secretion probably are key elements in morphogenesis and differentiation in Drosophila. In this study, we have analysed the effects of monensin, a Na+-H+-ionophore which blocks normal secretion, applied during cellular blastoderm formation on further development. Normal cell morphology and intercellular contacts are lost and the extracellular matrix becomes disorganized. Gastrulation is blocked and abnormal foldings can be observed. Cuticle phenotypes showed different degrees of ventral, dorsal, head and posterior defects. The results are discussed in the context of what is known about membrane and extracellular matrix proteins in Drosophila.
Insights
Disrupting protein secretion in Drosophila during early development with monensin causes severe defects in cell structure, gastrulation, and embryonic development. This highlights the critical role of extracellular matrix and membrane proteins in Drosophila morphogenesis.
Area of Science:
- Developmental Biology
- Cell Biology
- Genetics
Background:
- Proper secretion of extracellular matrix and membrane proteins is crucial for morphogenesis and differentiation.
- Disruptions in these processes can lead to developmental abnormalities.
Purpose of the Study:
- To investigate the effects of monensin, a secretion inhibitor, on Drosophila development during cellular blastoderm formation.
- To understand the role of extracellular matrix and membrane proteins in early Drosophila development.
Main Methods:
- Treatment of Drosophila embryos with monensin during cellular blastoderm formation.
- Observation of effects on cell morphology, intercellular contacts, and extracellular matrix organization.
- Analysis of gastrulation, cuticle phenotypes, and developmental defects.
Main Results:
- Monensin treatment led to loss of normal cell morphology and intercellular contacts.
- The extracellular matrix became disorganized, and gastrulation was blocked.
- Abnormal foldings and various degrees of ventral, dorsal, head, and posterior defects were observed in the cuticle phenotypes.
Conclusions:
- Inhibition of normal secretion by monensin severely impacts Drosophila development.
- This study underscores the essential roles of membrane and extracellular matrix proteins in Drosophila morphogenesis and differentiation.

