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瓜类果斑病抗性黄瓜茎的精细定位和候选基因分析。

Fine mapping and candidate gene analysis of gummy stem blight resistance in cucumber stem.

机构信息

Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.

Department of Plant Sciences, University of California, Davis, One Shield Avenue, Davis, CA, 95616, USA.

出版信息

Theor Appl Genet. 2022 Sep;135(9):3117-3125. doi: 10.1007/s00122-022-04172-2. Epub 2022 Jul 23.

Abstract

Two candidate genes (Csa6G046210 and Csa6G046240) were identified by fine-mapping gsb-s6.2 for gummy stem blight resistance in cucumber stem. Gummy stem blight (GSB) is a serious fungal disease caused by Didymella bryoniae, that affects cucumber yield and quality worldwide. However, no GSB-resistant genes have been identified in cucumber cultivars. In this study, the wild cucumber accession 'PI 183967' was used as a source of resistance to GSB in adult stems. An F population was mapped using resistant line 'LM189' and susceptible line 'LM6' derived from a cross between 'PI 183967' and '931'. By developing InDel and SNP markers, the gsb-s6.2 QTL on Chr. 6 was fine-mapped to a 34 kb interval harboring six genes. Gene Expression analysis after inoculation showed that two candidate genes (Csa6G046210 and Csa6G046240) were induced and differentially expressed between the resistant and susceptible parents, and may be involved in disease defense. Sequence alignment showed that Csa6G046210 encodes a multiple myeloma tumor-associated protein, and it harbored two nonsynonymous SNPs and one InDel in the third and the fourth exons, and two InDels in the TATA-box of the basal promoter region. Csa6G046240 encodes a MYB transcription factor with six variants in the AP2/ERF and MYB motifs in the promoter. These two candidate genes lay the foundation for revealing the mechanism of GSB resistance and may be useful for marker-assisted selection in cucumber disease-resistant breeding.

摘要

两个候选基因(Csa6G046210 和 Csa6G046240)通过对黄瓜茎部 gummy 茎腐病抗性基因 gsb-s6.2 的精细定位被鉴定出来。gummy 茎腐病(GSB)是一种由 Didymella bryoniae 引起的严重真菌病害,影响全球黄瓜的产量和质量。然而,在黄瓜品种中尚未鉴定出 GSB 抗性基因。本研究以野生黄瓜品系‘PI 183967’为抗源,用于成年茎部 gummy 茎腐病抗性。利用来自‘PI 183967’和‘931’杂交的抗性系‘LM189’和感病系‘LM6’构建了一个 F2 群体。通过开发 InDel 和 SNP 标记,将 Chr.6 上的 gsb-s6.2 QTL 精细定位到一个包含六个基因的 34kb 区间内。接种后基因表达分析表明,两个候选基因(Csa6G046210 和 Csa6G046240)在抗性和感病亲本之间被诱导并差异表达,可能参与疾病防御。序列比对表明,Csa6G046210 编码一个多发性骨髓瘤肿瘤相关蛋白,在第三和第四外显子中存在两个非同义 SNP 和一个 InDel,在基础启动子区域的 TATA 盒中存在两个 InDel。Csa6G046240 编码一个 MYB 转录因子,在启动子的 AP2/ERF 和 MYB 基序中有六个变体。这两个候选基因为揭示 GSB 抗性机制奠定了基础,可能对黄瓜抗病性育种中的标记辅助选择有用。

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