He Ting, Ren Zhaoyu, Muhae-Ud-Din Ghulam, Guo Qingyun, Liu Taiguo, Chen Wanquan, Gao Li
State Key Laboratory for Biology of Plant Disease and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.
Key Laboratory of Agricultural Integrated Pest Management, Qinghai University, Xining, China.
Front Plant Sci. 2022 Feb 22;13:823907. doi: 10.3389/fpls.2022.823907. eCollection 2022.
Kühn [synonym (Wallr.) Liro] can lead to a wheat common bunt, which is one of the most serious diseases affecting kernels, a serious reduction in grain yield, and losses can reach up to 80% in favorable environments. To understand how wheat tassels respond to , based on an RNA-Seq technology, we analyzed a host transcript accumulation on healthy wheat tassels and on tassels infected by the pathogen. Our results showed that 7,767 out of 15,658 genes were upregulated and 7,891 out of 15,658 genes were downregulated in wheat tassels. Subsequent gene ontology (GO) showed that differentially expressed genes (DEGs) are predominantly involved in biological processes, cellular components, and molecular functions. Additionally, Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that 20 pathways were expressed significantly during the infection of wheat with , while biosynthesis of amino acids, carbon metabolism, and starch and sucrose metabolism pathways were more highly expressed. Our findings also demonstrated that genes involved in defense mechanisms and myeloblastosis (MYB) transcription factor families were mostly upregulated, and the RNA-seq results were validated by quantitative real-time polymerase chain reaction (qRT-PCR). This is the first report on transcriptomics analysis of wheat tassels in response to , which will contribute to understanding the interaction of and wheat, and may provide higher efficiency control strategies, including developing new methods to increase the resistance of wheat crops to -caused wheat common bunt.
库恩[同义词(瓦尔.)利罗]可导致小麦腥黑穗病,这是影响麦粒的最严重病害之一,会使谷物产量严重降低,在适宜环境下损失可达80%。为了解小麦穗对[病原体名称缺失]的反应,我们基于RNA测序技术,分析了健康小麦穗和受该病原体感染的小麦穗上宿主转录本的积累情况。我们的结果表明,在小麦穗中,15658个基因中有7767个基因上调,15658个基因中有7891个基因下调。随后的基因本体(GO)分析表明,差异表达基因(DEGs)主要参与生物过程、细胞成分和分子功能。此外,京都基因与基因组百科全书(KEGG)富集分析表明,在小麦感染[病原体名称缺失]期间,有20条途径显著表达,而氨基酸生物合成、碳代谢以及淀粉和蔗糖代谢途径的表达更为强烈。我们的研究结果还表明,参与防御机制的基因和成髓细胞白血病(MYB)转录因子家族大多上调,并且RNA测序结果通过定量实时聚合酶链反应(qRT-PCR)得到验证。这是关于小麦穗对[病原体名称缺失]反应的转录组学分析的首次报告,这将有助于理解[病原体名称缺失]与小麦的相互作用,并可能提供更高效率的防治策略,包括开发新方法来提高小麦作物对[病原体名称缺失]引起的小麦腥黑穗病的抗性。