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果实对脐腐病的转录组反应及在脐腐病抗性中的功能分析

Transcriptome Response of Fruit to Top-Rot Disease and Functional Analysis of in Top-Rot Disease Resistance.

作者信息

Li Minggui, Lu Min, Wu Xiaomao, An Huaming

机构信息

Engineering Research Center of National Forestry and Grassland Administration for Rosa roxburghii, Agricultural College, Guizhou University, Guiyang 550025, People's Republic of China.

出版信息

Phytopathology. 2025 Jun;115(6):689-700. doi: 10.1094/PHYTO-01-25-0015-R. Epub 2025 Jun 6.

Abstract

Top-rot disease (TRD) in fruit is caused by . TRD has emerged as a significant concern due to its frequent occurrence and causing substantial economic losses. To understand the transcriptome response to TRD infection and identify candidate genes involved in TRD resistance, four critical time points (0, 24, 72, and 120 h postinoculation) for fruit tissues inoculated with the TRD pathogen were selected for RNA sequencing. A total of 1,890 differentially expressed genes were identified from the transcriptome data, including 1,051 upregulated and 839 downregulated genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses revealed that they were primarily involved in oxidoreductase activity and the synthesis and metabolism of secondary metabolites. Many putative transcription factor families, such as MYB, bHLH, AP2-EREBP, NAC, and WRKY, were also identified as being positively responsive to TRD infestation. Among the upregulated genes, exhibited the strongest response to TRD. Transient overexpression and gene silencing demonstrated that positively regulated TRD resistance in fruit, partially through promoting the expression of antioxidant-related genes and enhancing their enzyme activities. Collectively, the results facilitated a better understanding of the transcriptional response to TRD and offered candidate genes for developing an germplasm resource with improved TRD resistance.

摘要

果实顶部腐烂病(TRD)是由 引起的。由于TRD频繁发生并造成重大经济损失,它已成为一个重大问题。为了了解转录组对TRD感染的反应并确定参与TRD抗性的候选基因,选择了用TRD病原菌接种的果实组织的四个关键时间点(接种后0、24、72和120小时)进行RNA测序。从转录组数据中总共鉴定出1890个差异表达基因,其中包括1051个上调基因和839个下调基因。基因本体论和京都基因与基因组百科全书分析表明,它们主要参与氧化还原酶活性以及次生代谢物的合成和代谢。许多假定的转录因子家族,如MYB、bHLH、AP2-EREBP、NAC和WRKY,也被鉴定为对TRD侵染呈阳性反应。在上调基因中, 对TRD表现出最强的反应。瞬时过表达和基因沉默表明, 在 果实中通过部分促进抗氧化相关基因的表达并增强其酶活性来正向调节TRD抗性。总体而言,这些结果有助于更好地理解对TRD的转录反应,并为培育具有改良TRD抗性的 种质资源提供了候选基因。

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