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A-mating-type gene expression can drive clamp formation in the bipolar mushroom Pholiota microspora (Pholiota nameko)
Ruirong Yi1, Hiroyuki Mukaiyama, Takashi Tachikawa
1Faculty of Agriculture, Tottori University, 4-101 Koyama-cho Minami, Tottori 680-8553, Japan.
Abstract:
In the bipolar basidiomycete Pholiota microspora, a pair of homeodomain protein genes located at the A-mating-type locus regulates mating compatibility. In the present study, we used a DNA-mediated transformation system in P. microspora to investigate the homeodomain proteins that control the clamp formation. When a single homeodomain protein gene (A3-hox1 or A3-hox2) from the A3 monokaryon strain was transformed into the A4 monokaryon strain, the transformants produced many pseudoclamps but very few clamps. When two homeodomain protein genes (A3-hox1 and A3-hox2) were transformed either separately or together into the A4 monokaryon, the ratio of clamps to the clamplike cells in the transformants was significantly increased to ca. 50%. We therefore concluded that the gene dosage of homeodomain protein genes is important for clamp formation. When the sip promoter was connected to the coding region of A3-hox1 and A3-hox2 and the fused fragments were introduced into NGW19-6 (A4), the transformants achieved more than 85% clamp formation and exhibited two nuclei per cell, similar to the dikaryon (NGW12-163 x NGW19-6). The results of real-time reverse transcription-PCR confirmed that sip promoter activity is greater than that of the native promoter of homeodomain protein genes in P. microspora. Thus, we concluded that nearly 100% clamp formation requires high expression levels of homeodomain protein genes and that altered expression of the A-mating-type genes alone is sufficient to drive true clamp formation.
Insights
Gene dosage of homeodomain proteins in Pholiota microspora is crucial for clamp formation. High expression levels of these genes, driven by strong promoters, are essential for achieving true clamp formation, indicating altered A-mating-type gene expression drives this process.
Area of Science:
- Mycology
- Genetics
- Molecular Biology
Background:
- Mating compatibility in bipolar fungi like Pholiota microspora is regulated by homeodomain protein genes at the A-mating-type locus.
- Clamp formation is a key dikaryotic structure in basidiomycetes, essential for nuclear division and genetic exchange.
Purpose of the Study:
- To investigate the role of homeodomain proteins in controlling clamp formation in Pholiota microspora.
- To determine the effect of gene dosage and expression levels on clamp formation.
Main Methods:
- DNA-mediated transformation of Pholiota microspora monokaryon strains (A3 and A4) with homeodomain protein genes (A3-hox1, A3-hox2).
- Utilizing the sip promoter to drive high-level expression of homeodomain genes.
- Real-time reverse transcription-PCR to quantify gene expression levels.
Main Results:
- Transformation with single homeodomain genes resulted in pseudoclamps, while co-transformation increased clamp formation to approximately 50%.
- High-level expression using the sip promoter led to over 85% clamp formation and dikaryotic characteristics (two nuclei per cell).
- Sip promoter activity was confirmed to be higher than the native promoter of these genes.
Conclusions:
- Gene dosage of homeodomain proteins is critical for regulating clamp formation.
- Achieving nearly 100% clamp formation requires high expression levels of homeodomain protein genes.
- Altered expression of A-mating-type genes alone is sufficient to induce true clamp formation in Pholiota microspora.
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