Kobayashi Yasufumi, Hirakawa Hideki, Shirasawa Kenta, Nishimura Kazusa, Fujii Kenichiro, Oros Rolando, Almanza Giovanna R, Nagatoshi Yukari, Yasui Yasuo, Fujita Yasunari
Biological Resources and Post-harvest Division, Japan International Research Center for Agricultural Sciences (JIRCAS), Ibaraki, Japan.
Department of Frontier Research and Development, Kazusa DNA Research Institute, Chiba, Japan.
Front Plant Sci. 2024 Aug 19;15:1434388. doi: 10.3389/fpls.2024.1434388. eCollection 2024.
Quinoa is emerging as a key seed crop for global food security due to its ability to grow in marginal environments and its excellent nutritional properties. Because quinoa is partially allogamous, we have developed quinoa inbred lines necessary for molecular genetic analysis. Our comprehensive genomic analysis showed that the quinoa inbred lines fall into three genetic subpopulations: northern highland, southern highland, and lowland. Lowland and highland quinoa are the same species, but have very different genotypes and phenotypes. Lowland quinoa has relatively small grains and a darker grain color, and is widely tested and grown around the world. In contrast, the white, large-grained highland quinoa is grown in the Andean highlands, including the region where quinoa originated, and is exported worldwide as high-quality quinoa. Recently, we have shown that viral vectors can be used to regulate endogenous genes in quinoa, paving the way for functional genomics to reveal the diversity of quinoa. However, although a high-quality assembly has recently been reported for a lowland quinoa line, genomic resources of the quality required for functional genomics are not available for highland quinoa lines. Here we present high-quality chromosome-level genome assemblies for two highland inbred quinoa lines, J075 representing the northern highland line and J100 representing the southern highland line, using PacBio HiFi sequencing and dpMIG-seq. In addition, we demonstrate the importance of verifying and correcting reference-based scaffold assembly with other approaches such as linkage maps. The assembled genome sizes of J075 and J100 are 1.29 and 1.32 Gb, with contigs N50 of 66.3 and 12.6 Mb, and scaffold N50 of 71.2 and 70.6 Mb, respectively, comprising 18 pseudochromosomes. The repetitive sequences of J075 and J100 represent 72.6% and 71.5% of the genome, the majority of which are long terminal repeats, representing 44.0% and 42.7% of the genome, respectively. The assembled genomes of J075 and J100 were predicted to contain 65,303 and 64,945 protein-coding genes, respectively. The high quality genomes of these highland quinoa lines will facilitate quinoa functional genomics research on quinoa and contribute to the identification of key genes involved in environmental adaptation and quinoa domestication.
藜麦正成为全球粮食安全的关键种子作物,因为它能够在边缘环境中生长且具有优异的营养特性。由于藜麦是部分异花授粉植物,我们已培育出分子遗传分析所需的藜麦自交系。我们的全面基因组分析表明,藜麦自交系分为三个遗传亚群:北部高地、南部高地和低地。低地藜麦和高地藜麦是同一物种,但具有非常不同的基因型和表型。低地藜麦籽粒相对较小,籽粒颜色较深,在世界各地广泛进行试验种植。相比之下,白色、大粒的高地藜麦生长在安第斯高地,包括藜麦的起源地,作为优质藜麦出口到世界各地。最近,我们已表明病毒载体可用于调控藜麦中的内源基因,为功能基因组学揭示藜麦的多样性铺平了道路。然而,尽管最近报道了一个低地藜麦品系的高质量组装基因组,但高地藜麦品系尚无功能基因组学所需质量的基因组资源。在此,我们使用PacBio HiFi测序和dpMIG-seq技术,展示了两个高地藜麦自交系J075(代表北部高地亚群)和J100(代表南部高地亚群)的高质量染色体水平基因组组装。此外,我们证明了用连锁图谱等其他方法验证和校正基于参考的支架组装的重要性。J075和J100的组装基因组大小分别为1.29 Gb和1.32 Gb,重叠群N50分别为66.3 Mb和12.6 Mb,支架N50分别为71.2 Mb和70.6 Mb,包含18条假染色体。J075和J100的重复序列分别占基因组的72.6%和71.5%,其中大部分是长末端重复序列,分别占基因组的44.0%和42.7%。预测J075和J100的组装基因组分别包含65303个和64945个蛋白质编码基因。这些高地藜麦品系的高质量基因组将促进藜麦功能基因组学研究,并有助于鉴定参与环境适应和藜麦驯化的关键基因。