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冬瓜(Cogn.)枯萎病(尖孢镰刀菌)抗性基因的精细定位与特性分析

Fine mapping and characterization of Fusarium wilt ( f. sp. ) resistance gene in wax gourd ( Cogn.).

作者信息

Li Fahuo, Qin Jian, Li Jingying, Cheng Liang, He Xuehan, Zhong Xiaohui, Mo Yangpeng, Liang Han, Wang Peng, Li Yan, Wu Yongguan

机构信息

Vegetable Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, China.

Guangxi Key Laboratory of Vegetable Breeding and New Technology Development, Nanning, China.

出版信息

Front Plant Sci. 2025 May 26;16:1555316. doi: 10.3389/fpls.2025.1555316. eCollection 2025.

DOI:10.3389/fpls.2025.1555316
PMID:40491815
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12146367/
Abstract

Fusarium wilt (FW), caused by the plant fungus , causes severe economic losses in wax gourd ( Cogn.). Developing disease-resistant varieties is an effective measure. Currently, no reports exist on gene localization or cloning of genes associated with FW resistance in wax gourd. However, our team has identified an FW resistance gene and plans to apply it in resistant varieties. In this study, we used bulked segregant analysis sequencing and quantitative trait locus detection on 1,304 inbred lines derived from resistant GD68 and susceptible HM25 parents to identify FW resistance genes. We successfully identified a resistance locus between the 3M13.385 and 3M16.869 markers on chromosome 3, named . Fine mapping between markers 3M15.904 and 3M16.373 (469 kb apart) identified 22 candidate genes. The transcriptome, sequencing comparison, and qRT-PCR analyses suggested that the endochitinase gene is the resistance gene, with significant expression differences between the parents and a one-base mutation in the first exon. The study also revealed the roles of in plant hormones, transcription factors, phenylpropane metabolism, oxidation-reduction, disease progression, enzymes, and cell wall modification pathways, enhancing FW resistance in GD68. Finally, we identified two closely linked insertion-deletion markers that can assist in the transfer and utilization of the gene, significantly improving the screening rate of positive individual plants and reducing breeding time.

摘要

由植物真菌引起的枯萎病(FW)给冬瓜(Cogn.)造成了严重的经济损失。培育抗病品种是一种有效的措施。目前,尚无关于冬瓜中与FW抗性相关基因的定位或克隆的报道。然而,我们的团队已经鉴定出一个FW抗性基因,并计划将其应用于抗病品种中。在本研究中,我们对来自抗性亲本GD68和感病亲本HM25的1304个自交系进行了混合分组分析法测序和数量性状基因座检测,以鉴定FW抗性基因。我们成功地在3号染色体上的3M13.385和3M16.869标记之间鉴定出一个抗性位点,命名为 。在标记3M15.904和3M16.373(相距469 kb)之间进行精细定位,确定了22个候选基因。转录组、测序比较和qRT-PCR分析表明,内切几丁质酶基因 是抗性基因,亲本之间存在显著的表达差异,且第一个外显子中有一个单碱基突变。该研究还揭示了 在植物激素、转录因子、苯丙烷代谢、氧化还原、疾病进展、酶和细胞壁修饰途径中的作用,增强了GD68对FW的抗性。最后,我们鉴定出两个紧密连锁的插入缺失标记,可协助 基因的转移和利用,显著提高阳性单株的筛选率,缩短育种时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/57d9a296f9e6/fpls-16-1555316-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/2f34044e33e1/fpls-16-1555316-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/aa17db5ce59e/fpls-16-1555316-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/57d9a296f9e6/fpls-16-1555316-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/2f34044e33e1/fpls-16-1555316-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/06ef1c85aef4/fpls-16-1555316-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/36db37d0fd92/fpls-16-1555316-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/b2f2796fcfbc/fpls-16-1555316-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/aa17db5ce59e/fpls-16-1555316-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/208b/12146367/57d9a296f9e6/fpls-16-1555316-g007.jpg

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