Li Tang, Zheng Jinfang, Nousias Orestis, Yan Yuchen, Meinhardt Lyndel W, Goenaga Ricardo, Zhang Dapeng, Yin Yanbin
Nebraska Food for Health Center, Department of Food Science and Technology, University of Nebraska, Lincoln, NE 68588, USA.
Sustainable Perennial Crops Laboratory, United States Department of Agriculture, Agriculture Research Service, Beltsville, MD 20705, USA.
Plants (Basel). 2024 Feb 26;13(5):636. doi: 10.3390/plants13050636.
(cherimoya) is a species renowned for its delectable fruit and medicinal properties. In this study, we developed a chromosome-level genome assembly for the cherimoya 'Booth' cultivar from the United States. The genome assembly has a size of 794 Mb with a N50 = 97.59 Mb. The seven longest scaffolds account for 87.6% of the total genome length, which corresponds to the seven pseudo-chromosomes. A total of 45,272 protein-coding genes (≥30 aa) were predicted with 92.9% gene content completeness. No recent whole genome duplications were identified by an intra-genome collinearity analysis. Phylogenetic analysis supports that eudicots and magnoliids are more closely related to each other than to monocots. Moreover, the was found to be more closely related to the Laurales than the Piperales. Genome comparison revealed that the 'Booth' cultivar has 200 Mb less repeats than the Spanish cultivar 'Fino de Jete', despite their highly similar (>99%) genome sequence identity and collinearity. These two cultivars were diverged during the early Pleistocene (1.93 Mya), which suggests a different origin and domestication of the cherimoya. Terpene/terpenoid metabolism functions were found to be enriched in , while TNL (oll/Interleukin-1-BS-RR) disease resistance gene has been lost in during evolution. We have also identified a gene cluster that is potentially responsible for the biosynthesis of acetogenins, a class of natural products found exclusively in . The cherimoya genome provides an invaluable resource for supporting characterization, conservation, and utilization of genetic resources.
番荔枝(释迦果)是一种以其美味果实和药用特性而闻名的物种。在本研究中,我们为来自美国的番荔枝‘布斯’品种构建了一个染色体水平的基因组组装。该基因组组装大小为794 Mb,N50 = 97.59 Mb。七条最长的支架占基因组总长度的87.6%,对应于七条假染色体。共预测到45272个蛋白质编码基因(≥30个氨基酸),基因含量完整性为92.9%。通过基因组内共线性分析未发现近期的全基因组重复事件。系统发育分析支持真双子叶植物和木兰类植物彼此之间的关系比与单子叶植物的关系更密切。此外,发现番荔枝与樟目植物的关系比与胡椒目植物的关系更密切。基因组比较显示,尽管‘布斯’品种与西班牙品种‘菲诺·德·赫特’的基因组序列同一性和共线性高度相似(>99%),但‘布斯’品种的重复序列比‘菲诺·德·赫特’少200 Mb。这两个品种在更新世早期(193万年前)分化,这表明番荔枝有不同的起源和驯化过程。发现萜类/类萜代谢功能在番荔枝中富集,而TNL(oll/白细胞介素-1-BS-RR)抗病基因在进化过程中在番荔枝中丢失。我们还鉴定出一个基因簇,它可能负责番荔枝内酯的生物合成,番荔枝内酯是一类仅在番荔枝中发现的天然产物。番荔枝基因组为支持番荔枝遗传资源的表征、保护和利用提供了宝贵资源。