ICAR-National Bureau of Plant Genetic Resources, New Delhi, 110012, India.
ICAR-Indian Agricultural Statistics Research Institute, New Delhi, 110012, India.
Funct Integr Genomics. 2023 May 20;23(2):169. doi: 10.1007/s10142-023-01104-1.
Stripe rust (Sr), caused by Puccinia striiformis f. sp. tritici (Pst), is the most devastating disease that poses serious threat to the wheat-growing nations across the globe. Developing resistant cultivars is the most challenging aspect in wheat breeding. The function of resistance genes (R genes) and the mechanisms by which they influence plant-host interactions are poorly understood. In the present investigation, comparative transcriptome analysis was carried out by involving two near-isogenic lines (NILs) PBW343 and FLW29. The seedlings of both the genotypes were inoculated with Pst pathotype 46S119. In total, 1106 differentially expressed genes (DEGs) were identified at early stage of infection (12 hpi), whereas expressions of 877 and 1737 DEGs were observed at later stages (48 and 72 hpi) in FLW29. The identified DEGs were comprised of defense-related genes including putative R genes, 7 WRKY transcriptional factors, calcium, and hormonal signaling associated genes. Moreover, pathways involved in signaling of receptor kinases, G protein, and light showed higher expression in resistant cultivar and were common across different time points. Quantitative real-time PCR was used to further confirm the transcriptional expression of eight critical genes involved in plant defense mechanism against stripe rust. The information about genes are likely to improve our knowledge of the genetic mechanism that controls the stripe rust resistance in wheat, and data on resistance response-linked genes and pathways will be a significant resource for future research.
条锈病(Sr)由条形柄锈菌小麦专化型(Pst)引起,是对全球小麦种植国家构成严重威胁的最具破坏性疾病。培育抗性品种是小麦育种中最具挑战性的方面。抗性基因(R 基因)的功能及其影响植物-宿主相互作用的机制尚不清楚。在本研究中,通过涉及两个近等基因系(NILs)PBW343 和 FLW29 进行了比较转录组分析。两种基因型的幼苗均用 Pst 生理小种 46S119 接种。在早期感染(12 hpi)时,共鉴定出 1106 个差异表达基因(DEGs),而在 FLW29 中,在后期(48 和 72 hpi)观察到 877 和 1737 个 DEGs 的表达。鉴定的 DEGs 包括防御相关基因,包括假定的 R 基因、7 个 WRKY 转录因子、钙和激素信号相关基因。此外,参与受体激酶、G 蛋白和光信号转导的途径在抗性品种中表达较高,并且在不同时间点都很常见。实时定量 PCR 进一步证实了 8 个参与小麦条锈病抗性植物防御机制的关键基因的转录表达。这些基因的信息可能会提高我们对控制小麦条锈病抗性的遗传机制的认识,而与抗性反应相关的基因和途径的数据将成为未来研究的重要资源。