School of Agriculture, Food and Wine, Waite Research Institute, The University of Adelaide, PMB 1, Glen Osmond, SA, 5064, Australia.
South Australian Research and Development Institute, GPO Box 397, Adelaide, SA, 5001, Australia.
Theor Appl Genet. 2019 May;132(5):1309-1320. doi: 10.1007/s00122-019-03279-3. Epub 2019 Jan 18.
The cereal cyst nematode resistance locus Rha2 was mapped to a 978 kbp region on the long arm of barley chromosome 2H. Three candidate genes are discussed. The cereal cyst nematode (CCN) Heterodera avenae is a soil-borne obligate parasite that can cause severe damage to cereals. This research involved fine mapping of Rha2, a CCN resistance locus on chromosome 2H of barley. Rha2 was previously mapped relative to restriction fragment length polymorphisms (RFLPs) in two mapping populations. Anchoring of flanking RFLP clone sequences to the barley genome assembly defined an interval of 5077 kbp. Genotyping-by-sequencing of resistant and susceptible materials led to the discovery of potentially useful single nucleotide polymorphisms (SNPs). Assays were designed for these SNPs and applied to mapping populations. This narrowed the region of interest to 3966 kbp. Further fine mapping was pursued by crossing and backcrossing the resistant cultivar Sloop SA to its susceptible ancestor Sloop. Evaluation of F progeny confirmed that the resistance segregates as a single dominant gene. Genotyping of 9003 BCF progeny identified recombinants. Evaluation of recombinant BCF progeny narrowed the region of interest to 978 kbp. Two of the SNPs within this region proved to be diagnostic of CCN resistance across a wide range of barley germplasm. Fluorescence-based and gel-based assays were developed for these SNPs for use in marker-assisted selection. Within the candidate region of the reference genome, there are nine high-confidence predicted genes. Three of these, one that encodes RAR1 (a cysteine- and histidine-rich domain-containing protein), one that is predicted to encode an acetylglutamate kinase and one that is predicted to encode a tonoplast intrinsic protein, are discussed as candidate genes for CCN resistance.
麦类作物孢囊线虫抗性基因 Rha2 被定位到大麦 2H 染色体长臂的 978 kbp 区域。讨论了三个候选基因。麦类作物孢囊线虫(CCN) Heterodera avenae 是一种土壤传播的专性寄生虫,可对麦类作物造成严重损害。这项研究涉及到对大麦 2H 染色体上的 CCN 抗性基因 Rha2 的精细定位。Rha2 先前是相对于两个作图群体中的限制性片段长度多态性(RFLP)进行定位的。侧翼 RFLP 克隆序列与大麦基因组组装的锚定定义了 5077 kbp 的间隔。对抗性和敏感材料进行的测序分型导致发现了潜在有用的单核苷酸多态性(SNP)。为这些 SNP 设计了检测方法,并应用于作图群体。这将感兴趣的区域缩小到 3966 kbp。通过将抗性品种 Sloop SA 与其易感祖先 Sloop 进行杂交和回交,进一步进行了精细定位。对 F 后代的评估证实,抗性是由单个显性基因分离的。对 9003 个 BCF 后代的基因型分析确定了重组体。对重组 BCF 后代的评估将感兴趣的区域缩小到 978 kbp。在该区域内的两个 SNP 被证明在广泛的大麦种质资源中对 CCN 抗性具有诊断性。为这些 SNP 开发了基于荧光和凝胶的检测方法,用于标记辅助选择。在参考基因组的候选区域内,有九个高可信度预测的基因。其中三个,一个编码 RAR1(一种富含半胱氨酸和组氨酸的域蛋白),一个预测编码乙酰谷氨酸激酶,一个预测编码液泡内膜蛋白,被认为是 CCN 抗性的候选基因。