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两个番茄(S)类甜蛋白基因赋予对晚疫病更强的抗性()。

Two Tomato (S) Thaumatin-Like Protein Genes Confer Enhanced Resistance to Late Blight ().

作者信息

Zhu Haishan, Deng Minghua, Yang Zhengan, Mao Lianzhen, Jiang Shurui, Yue Yanling, Zhao Kai

机构信息

College of Horticulture and Landscape, Yunnan Agricultural University, Kunming 650201, China.

出版信息

Phytopathology. 2021 Oct;111(10):1790-1799. doi: 10.1094/PHYTO-06-20-0237-R. Epub 2021 Nov 3.

Abstract

Late blight (caused by ) poses a serious threat to tomato production but the number of late blight resistance genes isolated from tomato is limited, making resistance gene mining a high research priority. In this study, highly resistant CLN2037E and susceptible No. 5 tomato inbred lines were used to identify late blight resistance genes. Using transcriptome sequencing, we discovered 36 differentially expressed genes (DEGs), including 21 nucleotide binding site-leucine-rich repeat and 15 pathogenesis-related (PR) disease resistance genes. Cluster analysis and real-time quantitative PCR showed that these 36 genes possessed similar expression patterns in different inbred lines after inoculation with . Moreover, two genes with unique responses were chosen to verify their functions when exposed to : and , both of which were thaumatin-like protein genes and were clustered in the tomato genome. Functions of these two genes were identified by gene overexpression and gene editing technology. Overexpression and knockout of single and corresponded to an increase and decrease in resistance to late blight, respectively, and led to a greater change in disease resistance compared with . Cotransformation of dual genes resulted in a much greater effect than any single gene. This study provides novel candidate resistance genes for tomato breeding against late blight and insights into the interaction mechanisms between tomato and .

摘要

晚疫病(由……引起)对番茄生产构成严重威胁,但从番茄中分离出的晚疫病抗性基因数量有限,这使得抗性基因挖掘成为一项高度优先的研究任务。在本研究中,使用高抗的CLN2037E和感病的5号番茄自交系来鉴定晚疫病抗性基因。通过转录组测序,我们发现了36个差异表达基因(DEGs),包括21个核苷酸结合位点富含亮氨酸重复序列基因和15个病程相关(PR)抗病基因。聚类分析和实时定量PCR表明,这36个基因在接种……后在不同自交系中具有相似的表达模式。此外,选择了两个具有独特反应的基因来验证它们在暴露于……时的功能:……和……,这两个基因都是类甜蛋白基因,并且在番茄基因组中聚类。通过基因过表达和基因编辑技术鉴定了这两个基因的功能。单个……和……的过表达和敲除分别对应于对晚疫病抗性的增加和降低,并且……与……相比导致抗病性有更大的变化。双基因共转化产生的效果比任何单个基因都大得多。本研究为番茄抗晚疫病育种提供了新的候选抗性基因,并深入了解了番茄与……之间的相互作用机制。

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