Zhou Jia, Wang Feifei, Zhong Weiming, Zheng Qianming, Qi Yong, Shi Binbin, Liu Qing, Zhang Sheng, Wang Nan, Tang Dongmei
Guizhou Institute of Pomology Science, Guizhou Academy of Agricultural Science, Guiyang, 550006, China.
Guizhou Key Laboratory of Molecular Breeding for Characteristic Horticultural Crops, Guiyang, 550006, China.
Sci Data. 2025 Jul 31;12(1):1334. doi: 10.1038/s41597-025-05593-6.
In this study, we report a high-quality chromosome-level genome assembly of Actinidia chinensis var. chinensis 'Guimi No. 2'. This cultivar, discovered in Guizhou karst ecosystems, exhibits resistance to Pseudomonas syringae pv. actinidiae (Psa). Using a combination of MGI short-read sequencing, PacBio HiFi long-read sequencing, and Hi-C technology, we generated a genome assembly of 608.43 Mb with a contig N50 of 20.70 Mb, and 99.70% of the assembly was successfully anchored onto 29 pseudochromosomes. The quality value (QV) and the LTR Assembly Index (LAI) of the assembled genome were 72.23 and 10.10. The BUSCO analysis indicated that the genome assembly and gene model prediction were 98.40% and 96.56% complete, respectively. A total of 251.15 Mb of repetitive sequences and 45,986 protein-coding genes were annotated. This genome assembly provides critical insights into A. chinensis's genomic architecture and serves as a foundational resource for elucidating disease resistance mechanisms against Psa, while enabling comparative phylogenomic studies across the Actinidia genus.
在本研究中,我们报道了中华猕猴桃变种中华猕猴桃‘贵蜜2号’的高质量染色体级基因组组装。该品种发现于贵州喀斯特生态系统,对猕猴桃溃疡病菌(Psa)具有抗性。我们结合了MGI短读长测序、PacBio HiFi长读长测序和Hi-C技术,生成了一个大小为608.43 Mb的基因组组装,其重叠群N50为20.70 Mb,并且99.70%的组装序列成功锚定到29条假染色体上。组装基因组的质量值(QV)和LTR组装指数(LAI)分别为72.23和10.10。BUSCO分析表明,基因组组装和基因模型预测的完整性分别为98.40%和96.56%。共注释了251.15 Mb的重复序列和45,986个蛋白质编码基因。该基因组组装为中华猕猴桃的基因组结构提供了重要见解,是阐明抗Psa抗病机制的基础资源,同时也有助于开展猕猴桃属的比较系统基因组学研究。