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Updated: Jun 12, 2026

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
Published on: May 25, 2018
Adaptive Spo11 RNA editing gate optimizes meiosis I pace and mitotic proliferation while preserving ascospore
Mengchun Wu1, Junfeng Liu1, Jiahui Han2
1State Key Laboratory for Crop Stress Resistance and High-Efficiency Production, College of Plant Protection, Northwest A&F University, Yangling, Shaanxi 712100, China.
Abstract:
Spo11-mediated DNA double-strand breaks (DSBs) are essential for meiotic recombination, yet how Spo11 activity is temporally regulated during mitosis and fungal development remains unclear. In the fungal plant pathogen Fusarium graminearum, we found that FgSpo11 has a DSB-independent role delaying meiosis I and a DSB-dependent role critical for postmeiotic mitoses during ascosporogenesis. Loss of FgSpo11 accelerates meiosis I and causes excessive postmeiotic divisions, ultimately causing aborted ascospores. A premature stop codon (TAG) is corrected to tryptophan (TGG) by adenosine-to-inosine RNA editing exclusively during sexual reproduction, enabling full-length protein synthesis. A genomically "corrected" allele bypassing this editing preserves ascospore formation but causes meiotic and vegetative mitotic defects. Beyond its on-switch function, this editing acts as a tunable rheostat fine-tuning FgSpo11 dosage during meiosis. Evolutionary analyses reveal recurrent gain and loss of this editing, highlighting adaptive modulation of Spo11 deployment. This study uncovers a single-site RNA editing gate controlling a key meiotic regulator and illustrates transcriptome plasticity in reconciling life cycle demands in eukaryotic pathogens.
Insights
In Fusarium graminearum, RNA editing corrects a stop codon in FgSpo11, regulating its dosage for proper meiosis and development. This editing acts as a crucial switch for fungal sexual reproduction and mitotic control.
Area of Science:
- Molecular Biology
- Mycology
- Genetics
Background:
- Spo11-mediated DNA double-strand breaks (DSBs) are crucial for meiotic recombination.
- Temporal regulation of Spo11 activity during mitosis and fungal development is not well understood.
Purpose of the Study:
- Investigate the role of FgSpo11 in meiosis and postmeiotic mitoses in *Fusarium graminearum*.
- Elucidate the mechanism of FgSpo11 regulation, including the role of RNA editing.
Main Methods:
- Genetic analysis of *Fusarium graminearum* mutants.
- RNA editing analysis.
- Evolutionary analysis of Spo11 deployment.
Main Results:
- FgSpo11 has DSB-independent and DSB-dependent roles in meiosis and postmeiotic divisions.
- Adenosine-to-inosine RNA editing corrects a premature stop codon in FgSpo11 during sexual reproduction.
- This RNA editing fine-tunes FgSpo11 dosage, acting as a rheostat for meiotic regulation.
- Genomic correction bypassing RNA editing leads to meiotic and mitotic defects.
Conclusions:
- A single-site RNA editing event acts as a critical gatekeeper for FgSpo11 function during sexual reproduction.
- Transcriptome plasticity through RNA editing allows adaptation to life cycle demands in fungal pathogens.
- Recurrent gain and loss of this RNA editing suggest adaptive modulation of Spo11 function.
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