The nuclear activity of the actin-binding Moesin protein is necessary for gene expression in Drosophila
Csaba Bajusz1,2, Ildikó Kristó1, Csilla Abonyi1
1Eötvös Loránd Research Network (ELKH), Biological Research Centre, Szeged, Hungary.
Abstract:
Ezrin-Radixin-Moesin (ERM) proteins play an essential role in the cytoplasm by cross-linking actin filaments with plasma membrane proteins. Research has identified the nuclear localization of ERMs, as well as the involvement of a single Drosophila ERM protein, Moesin, in nuclear mRNA exports. However, the question of how important the nuclear activity of ERM proteins are for the life of an organism has so far not been explored. Here, we present the first attempt to reveal the in vivo relevance of nuclear localization of Moesin in Drosophila. With the help of a nuclear export signal, we decreased the amount of Moesin in the nuclei of the animals. Furthermore, we observed various developmental defects, demonstrating the importance of ERM function in the nucleus for the first time. Transcriptome analysis of the mutant flies revealed that the lack of nuclear Moesin function leads to expression changes in nearly 700 genes, among them heat-shock genes. This result together with additional findings revealed that in Drosophila the expression of protein chaperones requires the nuclear functions of Moesin. DATABASE: GEO accession number: GSE155778.
Insights
Nuclear Moesin protein is crucial for Drosophila development. Its absence causes developmental issues and affects gene expression, particularly heat-shock and protein chaperone genes, highlighting its vital nuclear role.
Area of Science:
- Cell Biology
- Developmental Biology
- Molecular Genetics
Background:
- Ezrin-Radixin-Moesin (ERM) proteins link actin cytoskeleton to the plasma membrane.
- Nuclear localization of ERMs and Moesin's role in mRNA export are known.
- The in vivo significance of nuclear ERM activity remains unexplored.
Purpose of the Study:
- To investigate the in vivo importance of nuclear Moesin localization in Drosophila.
- To demonstrate the essential role of nuclear ERM protein function for organismal development.
Main Methods:
- Engineered a nuclear export signal to reduce nuclear Moesin levels in Drosophila.
- Observed developmental phenotypes in genetically modified flies.
- Performed transcriptome analysis to identify gene expression changes.
Main Results:
- Reduced nuclear Moesin resulted in significant developmental defects.
- Nearly 700 genes showed altered expression in mutant flies.
- Nuclear Moesin function is essential for regulating heat-shock genes and protein chaperones.
Conclusions:
- Nuclear Moesin localization is critical for normal Drosophila development.
- Nuclear Moesin plays a key role in regulating gene expression, including stress-response genes.
- The study establishes the in vivo relevance of nuclear ERM protein activity.
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