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High-quality chromosome-scale assembly of the walnut (Juglans regia L.) reference genome

机译:核桃(Juglans Regia L.)参考基因组的高质量染色体级组装

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Background: The release of the first reference genome of walnut (Juglans regia L.) enabled many achievements in the characterization of walnut genetic and functional variation. However, it is highly fragmented, preventing the integration of genetic, transcriptomic, and proteomic information to fully elucidate walnut biological processes. Findings: Here, we report the new chromosome-scale assembly of the walnut reference genome (Chandler v2.0) obtained by combining Oxford Nanopore long-read sequencing with chromosome conformation capture (Hi-C) technology. Relative to the previous reference genome, the new assembly features an 84.4-fold increase in N50 size, with the 16 chromosomal pseudomolecules assembled and representing 95% of its total length. Using full-length transcripts from single-molecule real-time sequencing, we predicted 37,554 gene models, with a mean gene length higher than the previous gene annotations. Most of the new protein-coding genes (90%) present both start and stop codons, which represents a significant improvement compared with Chandler v1.0 (only 48%). We then tested the potential impact of the new chromosome-level genome on different areas of walnut research. By studying the proteome changes occurring during male flower development, we observed that the virtual proteome obtained from Chandler v2.0 presents fewer artifacts than the previous reference genome, enabling the identification of a new potential pollen allergen in walnut. Also, the new chromosome-scale genome facilitates in-depth studies of intraspecies genetic diversity by revealing previously undetected autozygous regions in Chandler, likely resulting from inbreeding, and 195 genomic regions highly differentiated between Western and Eastern walnut cultivars. Conclusion: Overall, Chandler v2.0 will serve as a valuable resource to better understand and explore walnut biology.
机译:背景:核桃(Juglans Regia L)的第一参考基因组的释放使许多成就在核桃遗传和功能变异的表征中。然而,它是高度碎片化的,防止遗传,转录组和蛋白质组学信息的整合完全阐明核桃生物过程。调查结果:这里,通过将牛津纳米孔长读取测序与染色体构象捕获(HI-C)技术相结合来报告核桃参考基因组(Chandler V2.0)的新染色体级组件。相对于先前的参考基因组,新组件的N50尺寸增加了84.4倍,具有16个染色体假调子组装并表示其总长度的95%。使用来自单分子实时测序的全长转录物,我们预测了37,554个基因模型,其平均基因长度高于先前的基因注释。大多数新的蛋白质编码基因(90%)既有启动和止锁密码子都存在显着改善,而与Chandler v1.0相比(仅为48%)。然后,我们测试了新的染色体级基因组对核桃研究不同领域的潜在影响。通过研究在雄性花发育期间发生的蛋白质组变化,我们观察到从Chandler V2.0获得的虚拟蛋白质组比以前的参考基因组呈现较少的伪像,从而能够鉴定核桃的新潜在花粉过敏原。此外,新的染色体 - 级基因组通过揭示了近亲中的近期未检测到的近似未检测到的自血对的自血小基因子,促进了内部遗传多样性的深入研究,并且是西部和东部核桃品种之间高度区分的195个基因组区域。结论:总体而言,钱德勒V2.0将作为更好地理解和探索核桃生物学的宝贵资源。

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