Chen Bao-Zheng, Yang Zi-Jiang, Yang Ling, Zhu Yi-Fan, Li Xu-Zhen, Wang Lei, Zhou Ye-Peng, Zhang Guang-Hui, Li Da-Wei, Dong Yang, Duan Sheng-Chang
College of Food Science and Technology, Yunnan Agricultural University, Kunming, Yunnan, China.
Yunnan Provincial Key Laboratory of Biological Big Data, Yunnan Agricultural University, Kunming, Yunnan, China.
Front Plant Sci. 2024 Nov 4;15:1469375. doi: 10.3389/fpls.2024.1469375. eCollection 2024.
is a significant plant in traditional Chinese medicine, valued for its edible and medicinal properties. However, the lack of available genomic resources has hindered further research.
This study presents the first chromosome-scale genome assembly of using PacBio CLR reads and Hi-C scaffolding technology. Additionally, Ks analysis and syntenic depth analysis were performed to elucidate its evolutionary history.
The final assembly yielded a high-quality genome of 679.20 Mb, which was anchored to 8 pseudo-chromosomes with an anchoring rate of 96.5% and a scaffold N50 of 80.50 Mb. The genome assembly showed a high completeness of 97.6% based on Benchmarking with Universal Single-Copy Orthologs (BUSCO) analysis. Repetitive elements constituted approximately 76.8% of the genome, with long terminal repeat retrotransposons (LTRs) accounting for about 39.17%. Ks and syntenic depth analyses revealed that the polyploidization history of three platycodonoid clade species involved only the γ-WGT event. Karyotype evolutionary analysis identified an ancestral karyotype with 9 protochromosomes for the three platycodonoid clade species. Moreover, non-WGD genes, particularly those arising from tandem duplications, were found to contribute significantly to gene family expansion.
These findings provide essential insights into the genetic diversity and evolutionary biology of , aiding its conservation and sustainable use.
是传统中药中的一种重要植物,因其可食用和药用特性而受到重视。然而,缺乏可用的基因组资源阻碍了进一步的研究。
本研究利用PacBio CLR reads和Hi-C支架技术首次对进行了染色体水平的基因组组装。此外,还进行了Ks分析和共线性深度分析以阐明其进化历史。
最终组装得到了一个高质量的679.20 Mb基因组,该基因组被锚定到8条假染色体上,锚定率为96.5%,支架N50为80.50 Mb。基于通用单拷贝直系同源基因(BUSCO)分析,基因组组装显示出97.6%的高完整性。重复元件约占基因组的76.8%,其中长末端重复逆转座子(LTRs)约占39.17%。Ks和共线性深度分析表明,三种桔梗类分支物种的多倍体化历史仅涉及γ-WGT事件。核型进化分析确定了三种桔梗类分支物种具有9条原始染色体的祖先核型。此外,发现非全基因组复制基因,特别是那些由串联重复产生的基因,对基因家族扩展有显著贡献。
这些发现为的遗传多样性和进化生物学提供了重要见解,有助于其保护和可持续利用。