Genome Informatics Facility, Office of Biotechnology, Iowa State University, Ames, IA, USA.
Department of Plant Pathology and Microbiology, Iowa State University, Ames, IA, USA.
Mol Ecol Resour. 2021 Oct;21(7):2407-2422. doi: 10.1111/1755-0998.13432. Epub 2021 Jun 10.
The soybean cyst nematode (Heterodera glycines) is a sedentary plant parasite that exceeds billion USD annually in yield losses. This problem is exacerbated by H. glycines populations overcoming the limited sources of natural resistance in soybean and by the lack of effective and safe alternative treatments. Although there are genetic determinants that render soybeans resistant to nematode genotypes, resistant soybeans are increasingly ineffective because their multiyear usage has selected for virulent H. glycines populations. Successful H. glycines infection relies on the comprehensive re-engineering of soybean root cells into a syncytium, as well as the long-term suppression of host defences to ensure syncytial viability. At the forefront of these complex molecular interactions are effectors, the proteins secreted by H. glycines into host root tissues. The mechanisms that control genomic effector acquisition, diversification, and selection are important insights needed for the development of essential novel control strategies. As a foundation to obtain this understanding, we created a nine-scaffold, 158 Mb pseudomolecule assembly of the H. glycines genome using PacBio, Chicago, and Hi-C sequencing. A Mikado consensus gene prediction produced an annotation of 22,465 genes using short- and long-read expression data. To evaluate assembly and annotation quality, we cross-examined synteny among H. glycines assemblies, and compared BUSCO across related species. To describe the predicted proteins involved in H. glycines' secretory pathway, we contrasted expression between preparasitic and parasitic stages with functional gene information. Here, we present the results from our assembly and annotation of the H. glycines genome and contribute this resource to the scientific community.
大豆胞囊线虫(Heterodera glycines)是一种定居型植物寄生虫,每年造成的产量损失超过 10 亿美元。这一问题因 H. glycines 种群克服了大豆中有限的天然抗性资源,以及缺乏有效和安全的替代处理方法而加剧。尽管存在使大豆对线虫基因型具有抗性的遗传决定因素,但由于多年来使用抗性大豆,选择出了毒力更强的 H. glycines 种群,因此抗性大豆的效果越来越差。成功的 H. glycines 感染依赖于将大豆根细胞全面重塑为合胞体,以及长期抑制宿主防御以确保合胞体的存活。在这些复杂的分子相互作用中处于前沿的是效应子,即 H. glycines 分泌到宿主根组织中的蛋白质。控制基因组效应子获取、多样化和选择的机制对于开发必要的新型控制策略是非常重要的。作为获得这些理解的基础,我们使用 PacBio、芝加哥和 Hi-C 测序创建了一个由 9 个支架组成的、大小为 158 Mb 的 H. glycines 基因组假分子组装。使用短读长和长读长表达数据,Mikado 共识基因预测生成了 22465 个基因的注释。为了评估组装和注释的质量,我们交叉检查了 H. glycines 组装之间的同线性,并比较了相关物种之间的 BUSCO。为了描述参与 H. glycines 分泌途径的预测蛋白,我们将未寄生和寄生阶段的表达进行了对比,并与功能基因信息进行了比较。在这里,我们展示了我们对 H. glycines 基因组的组装和注释结果,并将这一资源贡献给科学界。