QTL mapping and genome-wide association analysis reveal genetic loci and candidate gene for resistance to gray leaf spot in tropical and subtropical maize germplasm.

IF 4.4 1区 农林科学 Q1 AGRONOMY Theoretical and Applied Genetics Pub Date : 2024-11-13 DOI:10.1007/s00122-024-04764-0
Yanhui Pan, Fuyan Jiang, Ranjan K Shaw, Jiachen Sun, Linzhuo Li, Xingfu Yin, Yaqi Bi, Jiao Kong, Haiyang Zong, Xiaodong Gong, Babar Ijaz, Xingming Fan
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Abstract

Key message: Using QTL mapping and GWAS, two candidate genes (Zm00001d051039 and Zm00001d051147) were consistently identified across the three different environments and BLUP values. GWAS analysis identified the candidate gene, Zm00001d044845. These genes were subsequently validated to exhibit a significant association with maize gray leaf spot (GLS) resistance. Gray leaf spot (GLS) is a major foliar disease of maize (Zea mays L.) that causes significant yield losses worldwide. Understanding the genetic mechanisms underlying gray leaf spot resistance is crucial for breeding high-yielding and disease-resistant varieties. In this study, eight tropical and subtropical germplasms were crossed with the temperate germplasm Ye107 to develop a nested association mapping (NAM) population comprising 1,653 F2:8 RILs, consisting of eight recombinant inbred line (RIL) subpopulations, using the single-seed descent method. The NAM population was evaluated for GLS resistance in three different environments, and genotyping by sequencing of the NAM population generated 593,719 high-quality single-nucleotide polymorphisms (SNPs). Linkage analysis and genome-wide association studies (GWASs) were conducted to identify candidate genes regulating GLS resistance in maize. Both analyses identified 25 QTLs and 149 SNPs that were significantly associated with GLS resistance. Candidate genes were screened 20 Kb upstream and downstream of the significant SNPs, and three novel candidate genes (Zm00001d051039, Zm00001d051147, and Zm00001d044845) were identified. Zm00001d051039 and Zm00001d051147 were located on chromosome 4 and co-localized in both linkage (qGLS4-1 and qGLS4-2) and GWAS analyses. SNP-138,153,206 was located 0.499 kb downstream of the candidate gene Zm00001d051039, which encodes the protein IN2-1 homolog B, a homolog of glutathione S-transferase (GST). GSTs and protein IN2-1 homolog B scavenge reactive oxygen species under various stress conditions, and GSTs are believed to protect plants from a wide range of biotic and abiotic stresses by detoxifying reactive electrophilic compounds. Zm00001d051147 encodes a probable beta-1,4-xylosyltransferase involved in the biosynthesis of xylan in the cell wall, enhancing resistance. SNP-145,813,215 was located 2.69 kb downstream of the candidate gene. SNP-5,043,412 was consistently identified in three different environments and BLUP values and was located 8.788 kb downstream of the candidate gene Zm00001d044845 on chromosome 9. Zm00001d044845 encodes the U-box domain-containing protein 4 (PUB4), which is involved in regulating plant immunity. qRT-PCR analysis showed that the relative expression levels of the three candidate genes were significantly upregulated in the leaves of the TML139 (resistant) parent, indicating that these three candidate genes could be associated with resistance to GLS. The findings of this study are significant for marker-assisted breeding aimed at enhancing resistance to GLS in maize and lay the foundation for further elucidation of the genetic mechanisms underlying resistance to gray leaf spot in maize and breeding of new disease-resistant varieties.

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QTL 绘图和全基因组关联分析揭示了热带和亚热带玉米种质抗灰叶斑病的遗传位点和候选基因。
关键信息:利用 QTL 图谱和 GWAS,在三种不同环境和 BLUP 值中一致确定了两个候选基因(Zm00001d051039 和 Zm00001d051147)。GWAS 分析确定了候选基因 Zm00001d044845。随后验证了这些基因与玉米灰叶斑病(GLS)抗性的显著相关性。灰叶斑病(GLS)是玉米(Zea mays L.)的一种主要叶面病害,在全球范围内造成严重的产量损失。了解灰叶斑病抗性的遗传机制对于培育高产抗病品种至关重要。本研究采用单种子后裔法,将八个热带和亚热带种质与温带种质 Ye107 杂交,培育出一个嵌套关联图谱(NAM)群体,该群体由 1,653 个 F2:8 RILs 组成,包括八个重组近交系(RIL)亚群。对 NAM 群体在三种不同环境中的 GLS 抗性进行了评估,并通过测序对 NAM 群体进行了基因分型,产生了 593,719 个高质量的单核苷酸多态性(SNPs)。研究人员进行了连锁分析和全基因组关联研究(GWAS),以确定调控玉米 GLS 抗性的候选基因。这两项分析确定了与 GLS 抗性显著相关的 25 个 QTL 和 149 个 SNP。对显著 SNP 上下游 20 Kb 的候选基因进行了筛选,发现了三个新的候选基因(Zm00001d051039、Zm00001d051147 和 Zm00001d044845)。Zm00001d051039 和 Zm00001d051147 位于 4 号染色体上,并在连锁分析(qGLS4-1 和 qGLS4-2)和 GWAS 分析中共同定位。SNP-138,153,206位于候选基因Zm00001d051039下游0.499 kb处,该基因编码谷胱甘肽S-转移酶(GST)的同源蛋白IN2-1同源物B。谷胱甘肽 S 转移酶和蛋白 IN2-1 同源物 B 能清除各种胁迫条件下的活性氧,谷胱甘肽 S 转移酶被认为能通过解毒活性亲电化合物来保护植物免受各种生物和非生物胁迫。Zm00001d051147 编码一种可能的 beta-1,4-木糖基转移酶,参与细胞壁中木糖的生物合成,从而增强抗性。SNP-145,813,215 位于候选基因下游 2.69 kb。SNP-5,043,412在三种不同环境和BLUP值中被一致鉴定,位于9号染色体上候选基因Zm00001d044845下游8.788 kb处。qRT-PCR 分析表明,这三个候选基因在 TML139(抗性)亲本叶片中的相对表达水平显著上调,表明这三个候选基因可能与 GLS 的抗性有关。本研究的发现对旨在提高玉米抗GLS能力的标记辅助育种具有重要意义,并为进一步阐明玉米抗灰叶斑病的遗传机制和培育抗病新品种奠定了基础。
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来源期刊
CiteScore
9.60
自引率
7.40%
发文量
241
审稿时长
2.3 months
期刊介绍: Theoretical and Applied Genetics publishes original research and review articles in all key areas of modern plant genetics, plant genomics and plant biotechnology. All work needs to have a clear genetic component and significant impact on plant breeding. Theoretical considerations are only accepted in combination with new experimental data and/or if they indicate a relevant application in plant genetics or breeding. Emphasizing the practical, the journal focuses on research into leading crop plants and articles presenting innovative approaches.
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