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Fine Mapping and Characterization of Stripe Rust Resistance Gene YrAYH in Near-Isogenic Lines Derived from a Cross Involving Wheat Landrace Anyuehong

Crop Journal(2024)SCI 1区

State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China

Cited 2|Views43
Abstract
Stripe rust, caused by Puccinia striiformis f. sp. tritici (Pst), is a devastating disease in wheat worldwide. Discovering and characterizing new resistance genes/QTL is crucial for wheat breeding programs. In this study, we fine-mapped and characterized a stripe rust resistance gene, YRAYH, on chromosome arm 5BL in the Chinese wheat landrace Anyuehong (AYH). Evaluations of stripe rust response to prevalent Chinese Pst races in near-isogenic lines derived from a cross of Anyuehong and Taichung 29 showed that YrAYH conferred a high level of resistance at all growth stages. Fine mapping using a large segregating population of 9748 plants, narrowed the YRAYH locus to a 3.7 Mb interval on chromosome arm 5BL that included 61 annotated genes. Transcriptome analysis of two NIL pairs identified 64 upregulated differentially expressed genes (DEGs) in the resistant NILs (NILs-R). Annotations indicated that many of these genes have roles in plant disease resistance pathways. Through a combined approach of fine-mapping and transcriptome sequencing, we identified a serine/threonine-protein kinase SRPK as a candidate gene underlying YrAYH. A unique 25 bp insertion was identified in the NILs-R compared to the NILs-S and previously published wheat genomes. An InDel marker was developed and co-segregated with YrAYH. Agronomic trait evaluation of the NILs suggested that YrAYH not only reduces the impact of stripe rust but was also associated with a gene that increases plant height and spike length.
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Key words
Candidate gene analysis,Crop protection,Puccinia striiformis,Transcriptome analyses
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要点】:本研究通过细致的基因定位和转录组分析,成功鉴定了小麦抗条锈病基因YrAYH,并发现了与植物疾病抗性途径相关的关键候选基因。

方法】:研究采用近等基因系评价、细致的基因定位和转录组测序方法。

实验】:通过对抗条锈病反应的近等基因系进行评价,使用9748株植物的大规模分离群体将YrAYH基因座缩小至染色体臂5BL上的3.7 Mb区间,并利用转录组分析确定了一个丝氨酸/苏氨酸蛋白激酶SRPK作为候选基因。实验使用的数据集为近等基因系NILs-R和NILs-S的转录组数据,结果发现了一个独特的25 bp插入突变,并与YrAYH共分离。此外,对农艺性状进行了评估。