Institute of Food Crops, Yunnan Academy of Agricultural Sciences, Kunming, 650205, China.
Institute of Resource Plants, Yunnan University, Kunming, 650500, China.
Theor Appl Genet. 2024 Nov 13;137(12):266. doi: 10.1007/s00122-024-04764-0.
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.
利用 QTL 作图和 GWAS 分析,在三个不同环境和 BLUP 值中一致鉴定出两个候选基因(Zm00001d051039 和 Zm00001d051147)。GWAS 分析鉴定出候选基因 Zm00001d044845。随后对这些基因进行了验证,发现它们与玉米灰斑病(GLS)抗性显著相关。灰斑病(GLS)是玉米(Zea mays L.)的一种主要叶部病害,在全球范围内造成了显著的产量损失。了解灰斑病抗性的遗传机制对于培育高产和抗病品种至关重要。在这项研究中,使用单粒传代法,将 8 个热带和亚热带种质与温带种质 Ye107 杂交,开发了一个嵌套关联作图(NAM)群体,该群体包含 1653 个 F2:8 RILs,由 8 个重组自交系(RIL)亚群组成。在三个不同的环境中对 NAM 群体进行了 GLS 抗性评估,通过 NAM 群体的测序生成了 593719 个高质量的单核苷酸多态性(SNP)。进行了连锁分析和全基因组关联研究(GWAS),以鉴定调控玉米 GLS 抗性的候选基因。两种分析都鉴定出了 25 个 QTL 和 149 个与 GLS 抗性显著相关的 SNP。在显著 SNP 的上下游筛选候选基因,鉴定出了三个新的候选基因(Zm00001d051039、Zm00001d051147 和 Zm00001d044845)。Zm00001d051039 和 Zm00001d051147 位于 4 号染色体上,在连锁(qGLS4-1 和 qGLS4-2)和 GWAS 分析中都共定位。SNP-138153206 位于候选基因 Zm00001d051039 的下游 0.499 kb 处,该基因编码 IN2-1 同源物 B 蛋白,是谷胱甘肽 S-转移酶(GST)的同源物。GSTs 和蛋白 IN2-1 同源物 B 在各种胁迫条件下清除活性氧,GSTs 被认为通过解毒活性亲电化合物来保护植物免受广泛的生物和非生物胁迫。Zm00001d051147 编码参与细胞壁木聚糖生物合成的 β-1,4-木糖基转移酶,增强了抗性。SNP-145813215 位于候选基因的下游 2.69 kb 处。SNP-5043412 在三个不同的环境和 BLUP 值中都被一致鉴定出来,位于候选基因 Zm00001d044845 的下游 8.788 kb 处,Zm00001d044845 编码 U -box 结构域包含蛋白 4(PUB4),该蛋白参与调节植物免疫。qRT-PCR 分析显示,在抗性亲本 TML139 的叶片中,三个候选基因的相对表达水平显著上调,表明这三个候选基因可能与 GLS 抗性有关。这项研究的结果对于旨在提高玉米对 GLS 抗性的标记辅助育种具有重要意义,为进一步阐明玉米灰斑病抗性的遗传机制和培育新的抗病品种奠定了基础。