Shen Tao, Gao Huawei, Wang Chao, Zheng Yunxiao, Song Weibin, Hou Peng, Zhu Liying, Zhao Yongfeng, Song Wei, Guo Jinjie
State Key Laboratory of North China Crop Improvement and Regulation, North China Key Laboratory for Crop Germplasm Resources of Education Ministry, Hebei Sub-Center of National Maize Improvement Center of China, College of Agronomy, Hebei Agricultural University, Baoding 071051, China.
State Key Laboratory of Maize Bio-Breeding, National Maize Improvement Center, Department of Plant Genetics and Breeding, China Agricultural University, Beijing 100107, China.
Plants (Basel). 2025 Jul 26;14(15):2315. doi: 10.3390/plants14152315.
Corn smut, caused by , significantly threatens maize production. This study evaluated 199 maize inbred lines at the seedling stage under greenhouse conditions for resistance to , identifying 39 highly resistant lines. A genome-wide association study (GWAS) using the mrMLM model detected 19 significant single-nucleotide polymorphism (SNP) loci. Based on a linkage disequilibrium (LD) decay distance of 260 kb, 226 candidate genes were identified. Utilizing the significant loci chr1_244281660 and chr5_220156746, two kompetitive allele-specific PCR (KASP) markers were successfully developed. A PCR-based sequence-specific oligonucleotide probe hybridization technique applied to the 199 experimental lines and 60 validation lines confirmed polymorphism for both markers, with selection efficiencies of 48.12% and 43.33%, respectively. The tested materials were derived from foundational inbred lines of domestic and foreign origin. Analysis of 39 highly resistant lines showed that the advantageous alleles carrying thymine/cytosine (T/C) predominated at frequencies of 94.87% and 53.84%, respectively. The genotype TTCC conferred high resistance, while CCTT was highly susceptible. The resistance exhibited high heritability and significant gene-by-environment interaction. This work systematically dissects the genetic basis of common smut resistance in maize, identifies favorable alleles, and provides a novel KASP marker-based strategy for developing disease-resistant germplasm.
玉米瘤黑粉病由[病原体名称未给出]引起,对玉米生产构成重大威胁。本研究在温室条件下对199个玉米自交系进行苗期抗[病原体名称未给出]鉴定,筛选出39个高抗自交系。利用mrMLM模型进行全基因组关联研究(GWAS),检测到19个显著的单核苷酸多态性(SNP)位点。基于260 kb的连锁不平衡(LD)衰减距离,鉴定出226个候选基因。利用显著位点chr1_244281660和chr5_220156746,成功开发了两个竞争性等位基因特异性PCR(KASP)标记。将基于PCR的序列特异性寡核苷酸探针杂交技术应用于199个试验系和60个验证系,证实了两个标记的多态性,选择效率分别为48.12%和43.33%。测试材料来源于国内外基础自交系。对39个高抗系的分析表明,携带胸腺嘧啶/胞嘧啶(T/C)的优势等位基因频率分别为94.87%和53.84%。基因型TTCC表现为高抗,而CCTT表现为高感。抗性表现出高遗传力和显著基因与环境互作。本研究系统解析了玉米抗瘤黑粉病的遗传基础,鉴定出有利等位基因,并为抗病种质创新提供了基于KASP标记的新策略。