Key Laboratory of National Forestry and Grassland Administration, Beijing for Bamboo & Rattan Science and Technology, Institute of Gene Science and Industrialization for Bamboo and Rattan Resources, International Center for Bamboo and Rattan, Beijing, 100102, China.
College of Forestry, Basic Forestry and Proteomics Research Center, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
J Integr Plant Biol. 2024 Jun;66(6):1087-1105. doi: 10.1111/jipb.13592. Epub 2024 Jan 12.
Dendrocalamus brandisii (Munro) Kurz is a sympodial bamboo species with inimitable taste and flavorful shoots. Its rapid growth and use as high-quality material make this bamboo species highly valued for both food processing and wood applications. However, genome information for D. brandisii is lacking, primarily due to its polyploidy and large genome size. Here, we assembled a high-quality genome for hexaploid D. brandisii, which comprises 70 chromosomes with a total size of 2,756 Mb, using long-read HiFi sequencing. Furthermore, we accurately separated the genome into its three constituent subgenomes. We used Oxford Nanopore Technologies long reads to construct a transcriptomic dataset covering 15 tissues for gene annotation to complement our genome assembly, revealing differential gene expression and post-transcriptional regulation. By integrating metabolome analysis, we unveiled that well-balanced lignin formation, as well as abundant flavonoid and fructose contents, contribute to the superior quality of D. brandisii shoots. Integrating genomic, transcriptomic, and metabolomic datasets provided a solid foundation for enhancing bamboo shoot quality and developing efficient gene-editing techniques. This study should facilitate research on D. brandisii and enhance its use as a food source and wood material by providing crucial genomic resources.
巨龙竹(Dendrocalamus brandisii (Munro) Kurz)是一种合轴丛生型竹种,具有独特的口感和美味的笋。其生长迅速,且材质优质,在食品加工和木材应用方面都具有很高的价值。然而,巨龙竹的基因组信息尚未得到充分研究,主要是因为其多倍体性和庞大的基因组大小。在这里,我们使用长读长 HiFi 测序技术,成功组装了六倍体巨龙竹的高质量基因组,该基因组由 70 条染色体组成,总大小为 2756 Mb。此外,我们还准确地将基因组分离成其三个组成亚基因组。我们使用 Oxford Nanopore Technologies 的长读长构建了涵盖 15 种组织的转录组数据集,用于基因注释,以补充我们的基因组组装,揭示了差异表达基因和转录后调控。通过整合代谢组分析,我们揭示了均衡的木质素形成以及丰富的类黄酮和果糖含量,这有助于巨龙竹笋的优质特性。整合基因组、转录组和代谢组数据集为提高竹笋品质和开发高效基因编辑技术提供了坚实的基础。这项研究为巨龙竹的研究提供了重要的基因组资源,有助于增强其作为食物来源和木材材料的利用。