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A chromosome-scale genome assembly of mungbean (Vigna radiata)
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Background
Mungbean (Vigna radiata) is one of the most socio-economically important leguminous food crops of Asia and a rich source of dietary protein and micronutrients. Understanding its genetic makeup is crucial for genetic improvement and cultivar development.
Methods
In this study, we combined single-tube long-fragment reads (stLFR) sequencing technology with high-throughput chromosome conformation capture (Hi-C) technique to obtain a chromosome-level assembly of V. radiata cultivar ‘KUML4’.
Results
The final assembly of the V. radiata genome was 468.08 Mb in size, with a scaffold N50 of 40.75 Mb. This assembly comprised 11 pseudomolecules, covering 96.94% of the estimated genome size. The genome contained 253.85 Mb (54.76%) of repetitive sequences and 27,667 protein-coding genes. Our gene prediction recovered 98.3% of the highly conserved orthologs based on Benchmarking Universal Single-Copy Orthologs (BUSCO) analysis. Comparative analyses using sequence data from single-copy orthologous genes indicated that V. radiata diverged from V. mungo approximately 4.17 million years ago. Moreover, gene family analysis revealed that major gene families associated with defense responses were significantly expanded in V. radiata.
Conclusion
Our chromosome-scale genome assembly of V. radiata cultivar KUML4 will provide a valuable genomic resource, supporting genetic improvement and molecular breeding. This data will also be valuable for future comparative genomics studies among legume species.
Title: A chromosome-scale genome assembly of mungbean (Vigna radiata)
Description:
Background
Mungbean (Vigna radiata) is one of the most socio-economically important leguminous food crops of Asia and a rich source of dietary protein and micronutrients.
Understanding its genetic makeup is crucial for genetic improvement and cultivar development.
Methods
In this study, we combined single-tube long-fragment reads (stLFR) sequencing technology with high-throughput chromosome conformation capture (Hi-C) technique to obtain a chromosome-level assembly of V.
radiata cultivar ‘KUML4’.
Results
The final assembly of the V.
radiata genome was 468.
08 Mb in size, with a scaffold N50 of 40.
75 Mb.
This assembly comprised 11 pseudomolecules, covering 96.
94% of the estimated genome size.
The genome contained 253.
85 Mb (54.
76%) of repetitive sequences and 27,667 protein-coding genes.
Our gene prediction recovered 98.
3% of the highly conserved orthologs based on Benchmarking Universal Single-Copy Orthologs (BUSCO) analysis.
Comparative analyses using sequence data from single-copy orthologous genes indicated that V.
radiata diverged from V.
mungo approximately 4.
17 million years ago.
Moreover, gene family analysis revealed that major gene families associated with defense responses were significantly expanded in V.
radiata.
Conclusion
Our chromosome-scale genome assembly of V.
radiata cultivar KUML4 will provide a valuable genomic resource, supporting genetic improvement and molecular breeding.
This data will also be valuable for future comparative genomics studies among legume species.
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