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基于转录组分析比较表达三种不同基因的转基因马铃薯品系对特定小种的防御反应。

Comparison of defense responses of transgenic potato lines expressing three different genes to specific races based on transcriptome profiling.

作者信息

Yang Xiaohui, Guo Xiao, Chen Guangxia, Dong Daofeng, Liu Fang, Yang Yuanjun, Yang Yu, Li Guangcun

机构信息

Institute of Vegetables and Flowers, Shandong Academy of Agricultural Sciences, Molecular Biology Key Laboratory of Shandong Facility Vegetable/National Vegetable Improvement Center Shandong Subcenter/ Huang-Huai-Hai Region Scientific Observation and Experimental Station of Tuber and Root Crop, Ministry of Agriculture and Rural Affairs, Jinan, China.

Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences; Key Laboratory of Biology and Genetic Improvement of Tuber and Root Crop, Ministry of Agriculture and Rural Affairs, Beijing, China.

出版信息

PeerJ. 2020 May 5;8:e9096. doi: 10.7717/peerj.9096. eCollection 2020.

Abstract

Potato late blight, one of the most devastating diseases in potato, is caused by the oomycete . Over 20 resistance genes have been cloned including , , and . The distinctions between defense response mechanisms mediated by different resistance genes are still unclear. Here we performed transcriptome profiling in three transgenic lines, , , and and wild-type Desiree under inoculation with two isolates, 89148 (race 0) and CN152 (super race), using RNA-seq. Compared with wild type, specific differentially expressed genes (DEGs) were identified in the three transgenic lines. The highest number of DEGs occurred in transgenic , with 779 DEGs in response to isolate 89148 and 864 DEGs in response to infection by CN152, followed by transgenic lines with 408 DEGs for isolate 89148 and 267 DEGs for CN152. Based on gene ontology, the most common GO terms (15 for 89148 and 20 for CN152) were enriched in transgenic and lines. This indicates that the defense pathways mediated by and are more similar than those mediated by . Further separate GO analysis of up- or down-regulated DEGs showed that the down-regulated DEGs mainly functioned in mediating the resistance of potato to 89148 by response to stress biological process and to CN152 by oxidation reduction biological process. KEGG pathways of DNA replication, plant-pathogen interaction and pentose and glucuronate interconversions are unique for transgenic , , and lines in incompatible interactions. Quantitative real-time PCR experimental validation confirmed the induced expression of DEGs in the late blight resistance signaling pathway. Our results will lay a solid foundation for further understanding the mechanisms of plant-pathogen interactions, and provide a theoretical reference for durable resistance in potato.

摘要

马铃薯晚疫病是马铃薯最具毁灭性的病害之一,由卵菌引起。已克隆出20多个抗性基因,包括、和。不同抗性基因介导的防御反应机制之间的差异仍不清楚。在此,我们利用RNA测序技术,对接种两种疫霉菌株89148(0号生理小种)和CN152(超级生理小种)的三个转基因株系、和野生型德西蕾进行了转录组分析。与野生型相比,在三个转基因株系中鉴定出了特定的差异表达基因(DEG)。差异表达基因数量最多的是转基因株系,在接种89148菌株时有779个差异表达基因,在接种CN152菌株时有864个差异表达基因,其次是转基因株系,接种89148菌株时有408个差异表达基因,接种CN152菌株时有267个差异表达基因。基于基因本体论,最常见的GO术语(89148菌株有15个,CN152菌株有20个)在转基因和株系中富集。这表明由和介导的防御途径比由介导的防御途径更相似。对上调或下调的差异表达基因进行进一步的单独GO分析表明,下调的差异表达基因主要通过响应胁迫生物学过程介导马铃薯对89148菌株的抗性,并通过氧化还原生物学过程介导对CN152菌株的抗性。DNA复制、植物-病原体相互作用以及戊糖和葡萄糖醛酸相互转化的KEGG途径在转基因、和株系的不相容相互作用中是独特的。实时定量PCR实验验证证实了晚疫病抗性信号通路中差异表达基因的诱导表达。我们的结果将为进一步了解植物-病原体相互作用机制奠定坚实基础,并为马铃薯的持久抗性提供理论参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56e7/7207217/523c5a36dc0f/peerj-08-9096-g001.jpg

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