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Published on: July 30, 2014
A WD40 repeat protein regulates fungal cell differentiation and can be replaced functionally by the mammalian
Stefanie Pöggeler1, Ulrich Kück
1Lehrstuhl für Allgemeine und Molekulare Botanik, Ruhr-Universität Bochum, 44780 Bochum, Germany.
Abstract:
Fruiting body development in fungi is a complex cellular differentiation process that is controlled by more than 100 developmental genes. Mutants of the filamentous fungus Sordaria macrospora showing defects in fruiting body formation are pertinent sources for the identification of components of this multicellular differentiation process. Here we show that the sterile mutant pro11 carries a defect in the pro11 gene encoding a multimodular WD40 repeat protein. Complementation analysis indicates that the wild-type gene or C-terminally truncated versions of the wild-type protein are able to restore the fertile phenotype in mutant pro11. PRO11 shows significant homology to several vertebrate WD40 proteins, such as striatin and zinedin, which seem to be involved in Ca2+-dependent signaling in cells of the central nervous system and are supposed to function as scaffolding proteins linking signaling and eukaryotic endocytosis. Cloning of a mouse cDNA encoding striatin allowed functional substitution of the wild-type protein with restoration of fertility in mutant pro11. Our data strongly suggest that an evolutionarily conserved cellular process controlling eukaryotic cell differentiation may regulate fruiting body formation.
Insights
Researchers identified the pro11 gene, encoding a WD40 repeat protein, as crucial for fungal fruiting body development in Sordaria macrospora. Functional substitution with a related vertebrate protein highlights conserved mechanisms in eukaryotic cell differentiation.
Area of Science:
- Mycology
- Developmental Biology
- Genetics
Background:
- Fruiting body development in fungi is a complex process regulated by numerous developmental genes.
- Mutants with defects in this process are vital for identifying key genetic components.
- Sordaria macrospora serves as a model organism for studying fungal multicellular differentiation.
Purpose of the Study:
- To identify the gene responsible for defects in fruiting body formation in the sterile mutant pro11 of Sordaria macrospora.
- To investigate the function of the PRO11 protein and its role in fungal development.
- To explore evolutionary conservation of developmental pathways by functional complementation with vertebrate homologs.
Main Methods:
- Genetic complementation analysis of the pro11 mutant.
- Gene cloning and sequencing to identify the pro11 gene.
- Functional substitution experiments using a mouse cDNA encoding the homologous protein striatin.
Main Results:
- The sterile mutant pro11 contains a defect in the pro11 gene, which encodes a multimodular WD40 repeat protein.
- Wild-type gene or truncated versions restored fertility in the pro11 mutant, indicating PRO11's essential role.
- The mouse striatin protein functionally substituted for PRO11, restoring fertility in the mutant.
Conclusions:
- The PRO11 protein is essential for fruiting body development in Sordaria macrospora.
- PRO11 shares homology with vertebrate WD40 proteins involved in signaling and scaffolding, suggesting conserved functions.
- The study suggests an evolutionarily conserved cellular process regulates fungal fruiting body formation and eukaryotic cell differentiation.
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