| 孙圣洁,郭笑冉,陈 军,张 鑫,何家乐,张傲琰,张传量,宋鹏博,赵文莎,赵慧玲,卢 佳,魏俊杰,孙道杰.小麦株高全基因组关联分析及候选位点验证[J].麦类作物学报,2026,(8):1068 |
| 小麦株高全基因组关联分析及候选位点验证 |
| Genome-Wide Association Study of Plant Height in Wheat and Validation of the Candidate Loci |
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| DOI: |
| 中文关键词: 小麦 株高 全基因组关联分析 分子标记辅助育种 |
| 英文关键词:Wheat Plant height GWAS Marker-assisted breeding |
| 基金项目:国家重点研发计划项目(2016YFD0101802) |
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| 摘要点击次数: 130 |
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| 中文摘要: |
| 株高是影响小麦抗倒伏性和产量的重要农艺性状。为解析小麦株高的遗传基础并挖掘稳定调控位点,以来源于黄淮麦区的339份小麦自然群体为试验材料,结合9个环境下的株高表型数据和21K单核苷酸多态性(SNP)芯片基因型数据,采用混合线性模型开展全基因组关联分析(GWAS)。对关键关联区间进行连锁不平衡(LD)与单倍型分析,并利用包含327份材料、基于660K SNP芯片的自然群体进行跨群体验证,同时对关键区间进行基因注释并筛选候选基因。结果表明,共鉴定到66个与株高显著相关的稳定QTL。其中,在6D染色体490.34~492.42 Mb区间检测到一个新的主效稳定位点QPh.nwafu-6D,该位点在8个环境中稳定表达,平均表型变异解释率为8.23%;该区间可划分为2个LD区块,Block2中鉴定到3种单倍型,优势单倍型Block2_Hap1(频率84.1%)携带材料的株高显著低于其他单倍型,且在多个环境中与较高的千粒重显著相关。通过跨群体验证,核心SNP标记(SNP_Chr6D_492211566)Block2_Hap1基因型材料株高极显著低于Block2_Hap2基因型材料(P<0.001)。在该区间(490.34~492.42 Mb)进一步注释筛选到8个候选基因,功能上主要涉及激酶信号、转录调控、泛素化降解与激素响应等过程。 |
| 英文摘要: |
| Plant height(PH) is an important agronomic trait affecting lodging resistance and yield in wheat. To dissect the genetic basis of PH and identify stable loci, we analyzed a natural population of 339 wheat accessions from the Huang-Huai wheat region using PH phenotypes collected across nine environments and genotypes obtained with a 21K single nucleotide polymorphism(SNP) array. Genome-wide association study(GWAS) was conducted using a mixed linear model(MLM). Linkage disequilibrium(LD) and haplotype analyses were performed for the key associated interval, and the association was further validated in a natural population of 327 accessions genotyped with a 660K SNP array. Candidate genes within the target interval were annotated and prioritized. In total, 66 stable QTLs significantly associated with PH were identified. A novel major and stable QTL, QPh.nwafu-6D, was detected on chromosome 6D(490.34-492.42 Mb) and was consistently detected in eight environments, explaining 8.23% of the phenotypic variance on average. The interval was divided into two LD blocks. In Block2, three haplotypes were identified, and the favorable haplotype Block2_Hap1(frequency 84.1%) showed significantly reduced PH compared with other haplotypes and was significantly associated with higher thousand-kernel weight in multiple environments. In the validation population, accessions carrying the Block2_Hap1 genotype at the core SNP marker SNP_Chr6D_492211566 exhibited significantly lower PH than those with the Block2_Hap2 genotype(P<0.001). Eight candidate genes were further prioritized in this interval, mainly involved in kinase signaling, transcriptional regulation, ubiquitin-mediated protein degradation, and hormone responses. |
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