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利用长读长技术在普通小麦中导入俄罗斯麦蚜抗性基因。

Accessing a Russian Wheat Aphid Resistance Gene in Bread Wheat by Long-Read Technologies.

出版信息

Plant Genome. 2019 Jun;12(2). doi: 10.3835/plantgenome2018.09.0065.

Abstract

Russian wheat aphid (RWA) ( Kurdjumov) is a serious invasive pest of small-grain cereals and many grass species. An efficient strategy to defy aphid attacks is to identify sources of natural resistance and transfer resistance genes into susceptible crop cultivars. Revealing the genes helps understand plant defense mechanisms and engineer plants with durable resistance to the pest. To date, more than 15 RWA resistance genes have been identified in wheat ( L.) but none of them has been cloned. Previously, we genetically mapped the RWA resistance gene into an interval of 0.83 cM on the short arm of chromosome 7D and spanned it with five bacterial artificial chromosome (BAC) clones. Here, we used a targeted strategy combining traditional approaches toward gene cloning (genetic mapping and sequencing of BAC clones) with novel technologies, including optical mapping and long-read nanopore sequencing. The latter, with reads spanning the entire length of a BAC insert, enabled us to assemble the whole region, a task that was not achievable with short reads. Long-read optical mapping validated the DNA sequence in the interval and revealed a difference in the locus organization between resistant and susceptible genotypes. The complete and accurate sequence of the region facilitated the identification of new markers and precise annotation of the interval, revealing six high-confidence genes. Identification of as the most likely candidate opens an avenue for its validation through functional genomics approaches.

摘要

俄罗斯麦蚜(RWA)(Kurdjumov)是一种严重的小粒谷物和许多草本植物的入侵害虫。抵御蚜虫攻击的有效策略是识别天然抗性来源,并将抗性基因转移到易感作物品种中。揭示这些基因有助于了解植物的防御机制,并设计出具有持久抗虫性的植物。迄今为止,在小麦(L.)中已经鉴定出超过 15 个 RWA 抗性基因,但没有一个基因被克隆。此前,我们将 RWA 抗性基因遗传定位到 7D 染色体短臂上 0.83cM 的区间内,并通过五个细菌人工染色体(BAC)克隆将其覆盖。在这里,我们使用了一种靶向策略,将基因克隆的传统方法(遗传图谱和 BAC 克隆测序)与新技术(包括光学图谱和长读长纳米孔测序)相结合。后者的读长跨越 BAC 插入物的全长,使我们能够组装整个区域,这是短读长无法实现的任务。长读长光学图谱验证了该区间的 DNA 序列,并揭示了抗性和易感基因型在基因座组织上的差异。该区域的完整和准确序列有助于鉴定新的标记和区间的精确注释,揭示了六个高可信度基因。鉴定为最有可能的候选基因,为通过功能基因组学方法对其进行验证开辟了途径。

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